http://purl.org/dc/terms/
http://xmlns.com/foaf/0.1/
http://www.w3.org/2004/02/skos/core#
http://www.bridgmodel.org/owl/3.1#
2012-08-31
Biomedical Research Integrated Domain Group (BRIDG) Domain Analysis Model
http://purl.org/dc/dcmitype/Dataset
en-US
The Biomedical Research Integrated Domain Group (BRIDG) Model is a collaborative effort . The BRIDG model is an instance of a Domain Analysis Model (DAM). The goal of the BRIDG Model is to produce a shared view of the dynamic and static semantics for the domain of protocol-driven research and its associated regulatory artifacts. This domain of interest is further defined as:
Protocol-driven research and its associated regulatory artifacts: i.e. the data, organization, resources, rules, and processes involved in the formal assessment of the utility, impact, or other pharmacological, physiological, or psychological effects of a drug, procedure, process, or device on a human, animal, or other subject or substance plus all associated regulatory artifacts required for or derived from this effort, including data specifically associated with post-marketing adverse event reporting.
http://www.bridgmodel.org
BRIDG Semantic Coordination Committee (SCC)
mailto:bridgTHC-L@list.nih.gov
Clinical Data Interchange Standards Consortium (CDISC)
http://www.cdisc.org
Health Level Seven (HL7), Regulated Clinical Research Information Management (RCRIM) work group
http://www.hl7.org/Special/committees/rcrim/index.cfm
U.S. Food and Drug Administration (FDA)
http://nci.nih.gov
U.S. National Cancer Institute (NCI)
http://www.fda.gov
bridg:DataEntity
Abstract construct collecting all BRIDG classes together
bridg:SubDomain
Abstract construct collecting all BRIDG packages together
bridg:entityProperty
Grouper for attribute and association for situations where either may apply.
bridg:attributeProperty
Represents attributes of BRIDG classes
bridg:associationProperty
Represents associations between BRIDG classes
bridg:isAbstract
Identifies whether a class is considered "abstract" (i.e. not directly instantiatable)
bridg:DataEntity
xs:boolean
bridg:isDerived
Identifies whether a the semantics of a given attribute or association can be determined from other characteristics in the model. (At some point, these derivations might be formally expressed in OWL semantics.)
bridg:entityProperty
xs:boolean
none
shared
composite
bridg:associationType
Indicates the type of UML aggregation charactersitics an association shows
bridg:association
bridg:associationTypeDatatype
bridg:roleName
Indicates the role name when traversing the association to the target class
bridg:association
xs:string
bridg:constraint
Identifies a constraint that applies within the context of a class
bridg:BRIDG_Domain_Analysis_Model
BRIDG Domain Analysis Model
bridg:BRIDG_Domain_Analysis_Model
View Description:
This View shows the complete BRIDG Model (current Release) and specifically shows, for each class where it's applicable, the complete set of attributes for the class, partitioning the attributes as to whether they are "local" to the class or inherited from the class' super-type hierarchy.
bridg:Statistical_Analysis_Sub-Domain
Statistical Analysis Sub-Domain
bridg:Statistical_Analysis_Sub-Domain
View Description:
The Statistical Analysis Sub-Domain includes concepts describing the planning and performance of the statistical analysis of data collected during clinical trial research and their relationships. This sub-domain will eventually include the semantics for the entire Statistical Analysis lifecycle, but for BRIDG 3.2, only the Statistical Analysis Plan semantics are included.
bridg:Adverse_Event_Sub-Domain
Adverse Event Sub-Domain
bridg:Adverse_Event_Sub-Domain
View Description:
This view represents the Adverse Event (AE) semantics from the Adverse Event Domain Analysis Model, which was developed by representatives from several AE projects: HL7's Individual Case Safety Report (ICSR), CDISC's Study Data Tabulation Model for Human Subjects (SDTM), NCI's Cancer AE Reporting System (caAERS) and Adverse Event Expedited Reporting System (AdEERS), and the Federal Adverse Event Task Force (FAET).
The AE model introduced several new concept areas pertaining to devices, animals, and products.
There are 2 instance diagrams that illustrate the use of this view.
bridg:Adverse_Event_Sub-Domain
View Description:
The Adverse Event sub-domain is intended for those involved in safety related activities; such as detection, evaluation, follow-up and reporting. This includes safety issues involving people or products. It also includes activities during or after a research protocol.
bridg:Common_Sub-Domain
Common Sub-Domain
bridg:Common_Sub-Domain
View Description:
The Common sub-domain represents the semantics that are common to all (or most) of the other sub-domains. For example, it includes semantics for such things as people, organizations, places and materials.
bridg:Common_Sub-Domain
External Registry: We need an ontology of organization types. For Example, government, academic, pharmaceutical etc..
bridg:Protocol_Representation_Sub-Domain
Protocol Representation Sub-Domain
bridg:Protocol_Representation_Sub-Domain
View Description:
The Study Versioning View is intended to show the concepts within BRIDG that are related to a change in a study protocol; that is if a study protocol is changes what information needs to be kept about the old version. The majority of business requirements come from the C3PR project.
bridg:Protocol_Representation_Sub-Domain
View Description:
This View represents the core aspects of a protocol itself, the people, organizations and roles they may play in the context of a study.
Note: This view may absorb the Protocol-Driven Research and Study Design views in BRIDG 3.0.
bridg:Protocol_Representation_Sub-Domain
View Description:
The Protocol Representation sub-domain is intended for those involved in the planning and design of a research protocol. The majority of business requirements have come from those involved in clinical trial protocols. It focuses on the characteristics of a study and the definition and association of activities within the protocols, including "arms" and "epochs". It also includes the definitions of the roles that participate in those activities.
bridg:Protocol_Representation_Sub-Domain
Need to define the type of investigator
Study Principal Investigator will be defined as being responsible for the study as a whole (every protocol should have one Study Principal Investigator)
Site Principal Investigator will be person responsible for trial at a site
Other potential values for code list of roles:
• Coordinating Investigator (person coordinates multi-center site with satellite locations)
• Site Representative Investigator
• Investigator of Record
• Chief Investigator (defined as we define Study PI; new element from Clinical Trials European Directive, EMEA)
Modeling session should harmonize these values to develop a comprehensive list of values. In addition, the group discussed Credentialing information - while this is useful for regulatory purposes (1572), it may not be necessary for registries (see Notes for 6/14/05)
bridg:Protocol_Representation_Sub-Domain
View Description:
This view shows the core classes that collectively define protocol-driven research, the domain scoped/defined by the BRIDG model, i.e. the data, organization, resources, and processes involving the assessment of the utility, impact, or other pharmacological, physiological, or psychological effects of a drug, procedure, process, or device on a human, animal, or other biologic subject or substance plus all associated regulatory artifacts required or derived from said research.
Note that the THC has chosen to disambiguate the term "protocol" (and it's various overloaded terms including "trial" and "study" by defining a core class called StudyProtocol whose semantics enable a StudyProtocol to "contain" all of the various documents that collectively define the protocol and all of the activities that define the study. This view also includes the 'context' classes that are associated with the core StudyProtocol class. Finally, the class DocumentRelationship enables the documents collected in the course of a protocol's lifecycle (i.e. from planning to performing and beyond) to be related to each other with relationship types such as "updates," "replaces," "is a part of," "is an amendment to," etc.
bridg:Protocol_Representation_Sub-Domain
View Description:
This view is a representation of the CDISC Trial Design Model (TDM), NCI's Cancer Central Clinical Participant Registry (C3PR) Model and elements drawn from the CDISC HL7 Study Design message. Because of the complexity (and importance) of this model (as the basis for defining a computable representation of a study design) the THC has included several instance diagrams on the subject.
The different views of the design, the state-based view (used for planning and analysis) and the control-thread view (used for scheduling and execution), are described in the BRIDG Project Documentation and Release Notes for R1.1.
bridg:Regulatory_Sub-Domain
Regulatory Sub-Domain
bridg:Regulatory_Sub-Domain
View Description:
The Regulatory sub-domain is intended for those involved in the creation and review of submissions to regulatory authorities. The majority of business requirements come from the regulated product submission (RPS) message specification. It focuses on the documentation required for a product submission to the Food and Drug Administration (FDA).
bridg:Study_Conduct_Sub-Domain
Study Conduct Sub-Domain
bridg:Study_Conduct_Sub-Domain
status should be BRIDG status
bridg:Study_Conduct_Sub-Domain
This may me used by the External Registry group to model the drug intervention. Include other interventions like behavioral, vaccine, device, procedure.
bridg:Study_Conduct_Sub-Domain
Review SDTM and CTOM models
bridg:Study_Conduct_Sub-Domain
View Description:
The Study Conduct sub-domain is intended for those involved in the execution of a research study. The majority of business requirements have come from those involved in clinical trials. It focuses on the activities of conducting the study as well as the results from those activities.
bridg:Activity
Activity
bridg:Activity
true
bridg:Activity
Any action that can, in the context of a study or a post-marketing investigation, be defined, planned, scheduled or performed.
bridg:Activity
Administrative activities such as subject registration or informed consent
bridg:Activity
Clinical activities such as surgical procedure
bridg:Activity
laboratory test
bridg:Activity
administration of a drug
bridg:Activity
This is similar in idea to HL7 RIM's Act class
be participated in by Declaration
bridg:Activity
Unless constrained at any subclass level, all associations from Subject (including StudySubject) and ExperimentalUnit are valid for all activities.
bridg:Activity
urn:AE:Activity
bridg:Activity
urn:CTRPv1.0:Activity
bridg:Activity
urn:CTRPv3.8:Activity
bridg:Activity
urn:CTRRr3:Activity
bridg:Activity
urn:CTRv1.0:Activity
bridg:AdministrativeMemberCRA
AdministrativeMemberCRA
bridg:AdministrativeMemberCRA
false
bridg:AdministrativeMemberCRA
A clinical research associate (CRA) at a site who has the primary responsibility for communications and data related to a specific organizational network in which that site participates.
bridg:AdministrativeMemberCRA
Jane Doe is the Primary CRA for ECOG at Mayo Clinic; she receives all of the ECOG communications at Mayo and distributes them appropriately.
bridg:AdministrativeMemberCRA
urn:CoopGrp:AdministrativeMemberCRA
bridg:AdministrativeMemberPI
AdministrativeMemberPI
bridg:AdministrativeMemberPI
false
bridg:AdministrativeMemberPI
The principal investigator (PI) at a site who is responsible for all activities related to a specific organizational network's research at that site.
bridg:AdministrativeMemberPI
"Dr. Smith" is the ECOG site PI at Mayo Clinic. "Dr. Jones" is the site PI for the GOG network participation at Mayo Clinic. They are responsible for the overall management of the entire network's (ECOG
bridg:AdministrativeMemberPI
GOG) studies in which the Mayo Clinic participates.
bridg:AdministrativeMemberPI
urn:CoopGrp:AdministrativeMemberPI
bridg:AdverseEvent
AdverseEvent
bridg:AdverseEvent
false
bridg:AdverseEvent
Any unfavorable and unintended sign, symptom, disease, or other medical occurrence with a temporal association with the use of a medical product, procedure or other therapy, or in conjunction with a research study, regardless of causal relationship.
bridg:AdverseEvent
death
bridg:AdverseEvent
back pain
bridg:AdverseEvent
headache
bridg:AdverseEvent
pulmonary embolism
bridg:AdverseEvent
heart attack
bridg:AdverseEvent
The BRIDG SCC has a GForge Tracker Issue (#31893) indicating a need to validate the requirement that every AdverseEvent be described by a SafetyReportVersion.
bridg:AdverseEvent
urn:AE:AdverseEvent
bridg:AdverseEvent
urn:CTRv1.0:AdverseEvent
in IndividualCaseSafetyReport
bridg:AdverseEvent
urn:ICSRr2:AdverseEventAssessment
bridg:AdverseEvent
urn:NCI_CRF_Standard:AdverseEvent
bridg:AdverseEvent
urn:PSCv2.6:AdverseEvent
bridg:AdverseEvent
urn:SDTM_IGv3.1.2:AE.DOMAIN
bridg:AdverseEvent
urn:TDM:Incidents
bridg:AdverseEvent
urn:caAERSv2.2:AdverseEvent
bridg:AdverseEvent
urn:caAERSv2.2:ReportedAdverseEvent
bridg:AdverseEventOutcomeAssessment
AdverseEventOutcomeAssessment
bridg:AdverseEventOutcomeAssessment
false
bridg:AdverseEventOutcomeAssessment
The completed action of evaluating the final state of a subject or study subject who experienced an adverse event, which takes place after the adverse event occurs.
be participated in by Qualifier
bridg:AdverseEventOutcomeAssessment
Associations from Subject (including StudySubject) are valid for BiologicEntity and BiologicEntityGroup, not for Product, Specimen, HealthcareFacility or Organization. Associations from ExperimentalUnit are not valid.
bridg:AdverseEventOutcomeAssessment
urn:AE:Outcome
bridg:AdverseEventOutcomeAssessment
urn:CTRv1.0:AdverseEventOutcomeAssessment
bridg:AdverseEventOutcomeResult
AdverseEventOutcomeResult
bridg:AdverseEventOutcomeResult
false
bridg:AdverseEventOutcomeResult
The result of evaluating the final state of a person who experienced an adverse event.
bridg:AdverseEventOutcomeResult
Recovered/Resolved
bridg:AdverseEventOutcomeResult
Recovering/Resolving
bridg:AdverseEventOutcomeResult
Not Recovered/Not Resolved
bridg:AdverseEventOutcomeResult
Recovered/Resolved with Sequelae
bridg:AdverseEventOutcomeResult
Fatal
bridg:AdverseEventOutcomeResult
Unknown
bridg:AdverseEventOutcomeResult
urn:CTRv1.0:AdverseEventOutcomeResult
bridg:AdverseEventOutcomeResult
urn:SDTM_IGv3.1.1:AE.AEOUT
bridg:AdverseEventOutcomeResult
urn:caAERSv2.2:AdverseEventResponseDescription
bridg:AdverseEventSeriousness
AdverseEventSeriousness
bridg:AdverseEventSeriousness
false
bridg:AdverseEventSeriousness
Specifies the degree or extent of the consequence suffered by the subject or study subject.
bridg:AdverseEventSeriousness
resulted in death
bridg:AdverseEventSeriousness
required hospitalization
bridg:AdverseEventSeriousness
was life threatening
bridg:AdverseEventSeriousness
urn:CTRv1.0:AdverseEventSeriousness
bridg:AdverseEventSeriousness
urn:caAERSv2.2:Outcome
bridg:AmendmentChangeSummaryVersion
AmendmentChangeSummaryVersion
bridg:AmendmentChangeSummaryVersion
false
bridg:AmendmentChangeSummaryVersion
A document, memo or brief that enumerates the differences between two versions of a study protocol document.
bridg:AmendmentChangeSummaryVersion
Amendment
bridg:AmendmentChangeSummaryVersion
The term "Amendment" needs to be disambiguated since it sometimes refers to the amended version of the protocol (StudyProtocolDocumentVersion) and other times refers to the summary of changes (AmendmentChangeSummaryVersion) that are applied to a protocol to create a new version of the protocol.
bridg:AmendmentChangeSummaryVersion
urn:CTRv1.0:AmendmentChangeSummaryVersion
bridg:AmendmentChangeSummaryVersion
urn:PSCv2.6:Amendment
bridg:Animal
Animal
bridg:Animal
false
bridg:Animal
A non-human living organism that has membranous cell walls, requires oxygen and organic foods, and is capable of voluntary movement, as distinguished from a plant or mineral.
bridg:Animal
dog
bridg:Animal
cat
bridg:Animal
mouse
bridg:Animal
microorganism
bridg:Animal
urn:AE:Animal
bridg:Animal
urn:CTRv1.0:Animal
bridg:Animal
urn:HL7SD:Animal
bridg:Animal
urn:HL7SP:Animal
in IndividualCaseSafetyReport
bridg:Animal
urn:ICSRr2:Animal
bridg:Arm
Arm
bridg:Arm
false
bridg:Arm
A path through the study which describes what activities the study subject or experimental unit will be involved in as they pass through the study.
bridg:Arm
A study could have 2 arms named IV-Oral and Oral-IV. The name IV-Oral reflects a path that passes through IV treatment
bridg:Arm
then Oral treatment.
bridg:Arm
Group [CTRR Observational Studies]
bridg:Arm
An Arm is typically equivalent to a treatment group in a parallel design study. Generally, each subject is assigned to an arm, and the design of the study is reflected in the number and composition of the individual arms. This intended path through which the subject progresses in a study is composed of time point events (study cell) for each epoch of the study. Each time point event, in turn, has a pattern of child time points through which the subject would pass. This planned path thus describes how subjects assigned to the arm will be treated.
Mandatory Attribute Qualifier
bridg:Arm
At least one of the following attributes must be mandatory for Arm: name, typeCode.
armType Qualifier
bridg:Arm
armType is only valid for InterventionalStudyProtocolVersion.
name Unique
bridg:Arm
An Arm name must be unique within the context of the study that contains it.
bridg:Arm
urn:CTRPv1.0:Arm
bridg:Arm
urn:CTRPv3.8:Arm
bridg:Arm
urn:CTRRr3:Arm
bridg:Arm
urn:CTRv1.0:Arm
bridg:Arm
urn:HL7SD:Arm
bridg:Arm
urn:SDTM_IGv3.1.2:TA.DOMAIN
bridg:AssessedActivityRelationship
AssessedActivityRelationship
bridg:AssessedActivityRelationship
false
bridg:AssessedActivityRelationship
Specifies the link between an assessment (performed observation) and the performed activity that the assessment is based on.
bridg:AssessedActivityRelationship
The act of determining if graft failure occurred involves assessing a stem cell transplant.
bridg:AssessedResultRelationship
AssessedResultRelationship
bridg:AssessedResultRelationship
false
bridg:AssessedResultRelationship
Specifies the link between an assessment (performed observation) and the results of other performed observations that the assessment is based on.
bridg:AssessedResultRelationship
The acts of determining whether an adverse event occurred
bridg:AssessedResultRelationship
determining a diagnosis
bridg:AssessedResultRelationship
or determining a cause of death may each be based on evaluating several test results (PerformedObservation).
bridg:AssessedResultRelationship
urn:CTRv1.0:AssessedResultRelationship
in R_Product
bridg:AssessedResultRelationship
urn:ICSRr2:SequelTo
in IndividualCaseSafetyReport
bridg:AssessedResultRelationship
urn:ICSRr2:Subject10
in IndividualCaseSafetyReport
bridg:AssessedResultRelationship
urn:ICSRr2:Component2
in IndividualCaseSafetyReport
bridg:AssessedResultRelationship
urn:ICSRr2:component3
bridg:Assessor
Assessor
bridg:Assessor
false
bridg:Assessor
The person, organization, or device making an observation.
bridg:Assessor
healthcare provider
bridg:Assessor
adjudication committee
bridg:Assessor
family member
bridg:Assessor
radiologist
bridg:Assessor
vendor (may provide a uniform assessment for all sites participating in a study)
bridg:Assessor
heart rate monitor
bridg:Assessor
pace maker.
be a function performed by Exclusive Or
bridg:Assessor
Assessor might be a function performed by one and only one of the following: Subject, AssociatedBiologicEntity, HealthcareProvider, ResearchStaff, OversightCommittee, Laboratory, Device.
bridg:Assessor
urn:CTRv1.0:Assessor
in IndividualCaseSafetyReport
bridg:Assessor
urn:ICSRr2:AssignedEntity
in IndividualCaseSafetyReport
bridg:Assessor
urn:ICSRr2:AssignedEntity.code
in IndividualCaseSafetyReport
bridg:Assessor
urn:ICSRr2:Author1
in IndividualCaseSafetyReport
bridg:Assessor
urn:ICSRr2:Author2
bridg:Assessor
urn:SDTM_IGv3.1.1:CO.EVAL
bridg:Assessor
urn:SDTM_IGv3.1.1:EG.EVAL
bridg:Assessor
urn:SDTM_IGv3.1.1:PE.EVAL
bridg:AssociatedBiologicEntity
AssociatedBiologicEntity
bridg:AssociatedBiologicEntity
false
bridg:AssociatedBiologicEntity
An individual biologic entity connected/linked to another biologic entity.
bridg:AssociatedBiologicEntity
family member
bridg:AssociatedBiologicEntity
roommate
bridg:AssociatedBiologicEntity
nursing home attendant
Performer Scoper Type Unique
bridg:AssociatedBiologicEntity
A performer BiologicEntity and a scoper BiologicEntity may be associated to one another through AssociatedBiologicEntity more than once but the typeCode must be distinct (no duplicate performer/scoper/type triples).
bridg:AssociatedBiologicEntity
urn:AE:PersonalRelationship
bridg:AssociatedBiologicEntity
urn:CTRv1.0:AssociatedBiologicEntity
bridg:AssociatedBiologicEntity
urn:HL7SD:Role
bridg:AssociatedBiologicEntity
urn:HL7SP:Role
bridg:AssociatedBiologicEntity
urn:HL7SP:LivingSubject
in IndividualCaseSafetyReport
bridg:AssociatedBiologicEntity
urn:ICSRr2:Role2
in IndividualCaseSafetyReport
bridg:AssociatedBiologicEntity
urn:ICSRr2:ContactParty2
in IndividualCaseSafetyReport
bridg:AssociatedBiologicEntity
urn:ICSRr2:Role
bridg:Biologic
Biologic
bridg:Biologic
false
bridg:Biologic
A substance made from a living organism or thing it produces.
bridg:Biologic
virus
bridg:Biologic
therapeutic serum
bridg:Biologic
toxin
bridg:Biologic
antitoxin
bridg:Biologic
vaccine
bridg:Biologic
blood
bridg:Biologic
blood component or derivative
bridg:Biologic
allergenic product
bridg:Biologic
analogous product
bridg:Biologic
urn:CTRPv1.0:Biologic
bridg:Biologic
urn:CTRRr3:Biologic
bridg:Biologic
urn:CTRv1.0:Biologic
bridg:BiologicEntity
BiologicEntity
bridg:BiologicEntity
true
bridg:BiologicEntity
Any individual living (or previously living) being.
bridg:BiologicEntity
animal
bridg:BiologicEntity
human being
bridg:BiologicEntity
organism
Attribute Set actualIndicator Qualifier
bridg:BiologicEntity
name, birthDate, deathDate are valid only when actualIndicator = "true".
functions as PlannedStudySubject Qualifier
bridg:BiologicEntity
A BiologicEntity cannot be a PlannedStudySubject of a study if it is part of a BiologicEntityGroup that is a PlannedStudySubject of the same Study.
functions as StudySubject Qualifier
bridg:BiologicEntity
A BiologicEntity cannot be a StudySubject of a study if it is part of a BiologicEntityGroup that is a StudySubject of the same Study.
bridg:BiologicEntity
urn:AE:Organism
bridg:BiologicEntity
urn:CTRRr3:BiologicEntity
bridg:BiologicEntity
urn:CTRv1.0:BiologicEntity
bridg:BiologicEntity
urn:HL7SP:Access
bridg:BiologicEntityGroup
BiologicEntityGroup
bridg:BiologicEntityGroup
false
bridg:BiologicEntityGroup
A collection of biologic entities.
bridg:BiologicEntityGroup
flock of ducks
bridg:BiologicEntityGroup
litter of mice
bridg:BiologicEntityGroup
herd of cows
Attribute Set actualIndicator Qualifier
bridg:BiologicEntityGroup
name is valid only when actualIndicator = "true".
contain actualIndicator Qualifier
bridg:BiologicEntityGroup
containedBiologicEntityGroup must have the same value for actualIndicator as their containingBiologicEntityGroup.
bridg:BiologicEntityGroup
urn:AE:Group
bridg:BiologicEntityGroup
urn:CTRv1.0:BiologicEntityGroup
bridg:BiologicEntityGroup
urn:HL7SP:GroupKind
bridg:BiologicEntityGroup
urn:HL7SP:Member
bridg:BiologicEntityIdentifier
BiologicEntityIdentifier
bridg:BiologicEntityIdentifier
false
bridg:BiologicEntityIdentifier
The unique identification of a biologic entity in a specified context.
bridg:BiologicEntityIdentifier
This class is a resolution of the requirement for noting the type of an identifier which is not handled by the purely technical HL7 II data type.
identifies actualIndicator Qualifier
bridg:BiologicEntityIdentifier
Only BiologicEntity with actualIndicator = "true" is valid.
is assigned by actualIndicator Qualifier
bridg:BiologicEntityIdentifier
Only Organization with actualIndicator = "true" is valid.
bridg:BiologicEntityIdentifier
urn:AE:PersonIdentifier
bridg:BiologicEntityIdentifier
urn:CTRPv1.0:IdentifiedBiologicEntity
bridg:BiologicEntityIdentifier
urn:CTRPv3.8:IdentifiedEntity
bridg:BiologicEntityIdentifier
urn:CTRRr3:BiologicEntityIdentifier
bridg:BiologicEntityIdentifier
urn:CTRv1.0:BiologicEntityIdentifier
bridg:BiologicEntityIdentifier
urn:HCTv1.0:MD_Anderson_Specific_Content:_Donor.Donor_medical_record_number
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier
urn:ICSRr2:IdentifiedEntity2
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier
urn:ICSRr2:IdentifiedEntity
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier
urn:ICSRr2:IdentifiedEntity3
bridg:BiologicEntityPart
BiologicEntityPart
bridg:BiologicEntityPart
false
bridg:BiologicEntityPart
A limb, organ, or other portion of a biologic entity.
bridg:BiologicEntityPart
the left kidney of a person
bridg:BiologicEntityPart
a dog's right front paw
bridg:BiologicEntityPart
a patch of skin on a person's left forearm
quantity actualIndicator Qualifier
bridg:BiologicEntityPart
quantity shall only be permitted when the BiologicEntity.actualIndicator="false" and the BiologicEntityPart does not have an association to ExperimentalUnit.
bridg:BiologicEntityPart
urn:CTRRr3:BiologicEntityPart
bridg:BiologicEntityPart
urn:CTRv1.0:BiologicEntityPart
bridg:BiologicEntityPart
urn:HL7SD:Access
bridg:CausalAssessment
CausalAssessment
bridg:CausalAssessment
false
bridg:CausalAssessment
The judgment of relatedness between an adverse event and an activity or observation result.
bridg:CausalAssessment
The observation result of "diabetes" is assessed to have caused the AE.
bridg:CausalAssessment
The activity of administering a concomitant medication is assessed to have caused the AE.
bridg:CausalAssessment
The activity of administering the study drug is assessed to have caused the AE.
be participated in by Qualifier
bridg:CausalAssessment
Associations from Subject (including StudySubject) are valid for BiologicEntity and BiologicEntityGroup, not for Product, Specimen, HealthcareFacility or Organization. Associations from ExperimentalUnit are not valid.
bridg:CausalAssessment
urn:AE:CausalAssessment
bridg:CausalAssessment
urn:CTRv1.0:CausalAssessment
in IndividualCaseSafetyReport
bridg:CausalAssessment
urn:ICSRr2:AdverseEffectReference
in IndividualCaseSafetyReport
bridg:CausalAssessment
urn:ICSRr2:Subject2
in IndividualCaseSafetyReport
bridg:CausalAssessment
urn:ICSRr2:Subject4
in IndividualCaseSafetyReport
bridg:CausalAssessment
urn:ICSRr2:CausalityAssessment
in IndividualCaseSafetyReport
bridg:CausalAssessment
urn:ICSRr2:Component1
bridg:CollectingLaboratory
CollectingLaboratory
bridg:CollectingLaboratory
false
bridg:CollectingLaboratory
The laboratory that collects the specimen from an experimental unit.
bridg:CollectingLaboratory
urn:CTRv1.0:CollectingLaboratory
bridg:CollectingLaboratory
urn:LabViewer2.2:CentralLaboratory
bridg:CompanionStudyRelationship
CompanionStudyRelationship
bridg:CompanionStudyRelationship
false
bridg:CompanionStudyRelationship
Specifies the link between a parent study and a companion study.
bridg:CompanionStudyRelationship
The relationship exists between the version of the parent study and the non-versioned concept of the companion study because the relationship may be added in a new version of the parent study and references the overall notion of the companion study, not a particular version of the companion study.
bridg:CompanionStudyRelationship
urn:C3PRv2.9:CompanionStudyAssociation
bridg:CompanionStudyRelationship
urn:CTRv1.0:CompanionStudyRelationship
bridg:ConcomitantAgent
ConcomitantAgent
bridg:ConcomitantAgent
false
bridg:ConcomitantAgent
Substance used by the study subject either prior to or during the study that are not specified by the protocol.
bridg:ConcomitantAgent
Blood pressure medication prescribed either before or during a chemotherapy therapeutic trial.
bridg:ConcomitantAgent
tobacco
bridg:ConcomitantAgent
alcohol
bridg:ConcomitantAgent
DEPRECATED in BRIDG 3.1 because it was determined that the distinction between StudyAgent and ConcomitantAgent is no longer needed for performed activities (it was never made for defined activities). To be consistent all associations from (defined and performed) activities will now be directly to Product. StudyAgent will only be associated to StudyProtocolVersion, not to any activities. ConcomitantAgent is no longer needed.
BRIDG does not yet have a business requirement to include illicit use of drugs or abuse of drugs as concomitant agents.
bridg:ConcomitantAgent
urn:CTRv1.0:ConcomitantAgent
bridg:CooperativeGroup
CooperativeGroup
bridg:CooperativeGroup
false
bridg:CooperativeGroup
A group of researchers, cancer centers, and community doctors who provide infrastructure for studies of new cancer treatment, prevention, early detection, quality of life, and rehabilitation.
bridg:CooperativeGroup
Eastern Cooperative Oncology Group (ECOG)
bridg:CooperativeGroup
Southwest Oncology Group (SWOG).
bridg:CooperativeGroup
urn:CoopGrp:CooperativeGroup
bridg:CooperativeGroupMember
CooperativeGroupMember
bridg:CooperativeGroupMember
false
bridg:CooperativeGroupMember
An organization comprised of a group of treating sites.
bridg:CooperativeGroupMember
A group of cancer centers with outreach clinics forming a loose confederation for research purposes.
bridg:CooperativeGroupMember
urn:CoopGrp:MemberInstitution
bridg:Cosmetic
Cosmetic
bridg:Cosmetic
false
bridg:Cosmetic
An article intended to be rubbed, poured, sprinkled, or sprayed on or introduced into or otherwise applied to the human body for cleansing, beautifying, promoting attractiveness or altering the appearance.
bridg:Cosmetic
urn:CTRPv1.0:Cosmetic
bridg:Cosmetic
urn:CTRv1.0:Cosmetic
bridg:DataMonitoringCommitteeCharterVersion
DataMonitoringCommitteeCharterVersion
bridg:DataMonitoringCommitteeCharterVersion
false
bridg:DataMonitoringCommitteeCharterVersion
A key document that, together with the study protocol and Statistical Analysis Plan (SAP), prospectively defines the study's Data Monitoring Committee (DMC) infrastructure and, in particular, the DMC's responsibilities; stipulates who sees blinded results and who sees unblinded results; and establishes a method for communication between the DMC and the sponsor.
bridg:DataMonitoringCommitteeCharterVersion
urn:Statistics_v1.0:DataMonitoringCommitteeCharter
bridg:DefinedActivity
DefinedActivity
bridg:DefinedActivity
false
bridg:DefinedActivity
An activity that frequently occurs in studies (e.g. more than one time in more than one arm) and therefore is called out as a reusable template in a global library of activities outside the context of any particular study, and may be used in the composition of a defined subject activity group. A defined activity is a "kind of" activity rather than an "instance of" an activity.
bridg:DefinedActivity
Standard blood chemistries are frequently included in studies - also activities that are study-specific and recur more than one time in more than one arm may be defined
bridg:DefinedActivity
such as a substance administration activity involving X amount of drug Y.
bridg:DefinedActivity
A defined activity is represented here as a subtype of Activity, but could also be thought of as an activity at a particular stage in the business process in which the activities occur, i.e., in the "defined" stage rather than the "planned" stage, the "scheduled" stage or the "performed" stage.
Repeat Duration or Quantity Exclusive Or
bridg:DefinedActivity
A DefinedActivity may have a value for one and only one of the following: repeatDuration or repeatQuantity.
Repeat Frequency Exclusive Or
bridg:DefinedActivity
A DefinedActivity may have a value for one and only one of the following: repeatFrequencyCode or repeatFrequencyRatio.
be participated in by actualIndicator Qualifier
bridg:DefinedActivity
Only BiologicEntity, BiologicEntityGroup, Material, ProductGroup or Organization (via Subject or ExperimentalUnit) with actualIndicator = “false” is valid.
bridg:DefinedActivity
urn:CTRRr3:DefinedActivity
bridg:DefinedActivity
urn:CTRv1.0:DefinedActivity
bridg:DefinedActivity
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Act.priorityCode
bridg:DefinedActivity
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Supply.quality
bridg:DefinedActivity
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Encounter.priorityCode
bridg:DefinedActivity
urn:PSCv2.6:Activity
bridg:DefinedAdministrativeActivity
DefinedAdministrativeActivity
bridg:DefinedAdministrativeActivity
false
bridg:DefinedAdministrativeActivity
An activity defined at a global library level that is not directly related to hypothesis evaluation or testing, but is typically essential to the efficient and/or effective coordination and execution of a study.
bridg:DefinedAdministrativeActivity
assignment to a treatment arm
bridg:DefinedAdministrativeActivity
registration to a study
bridg:DefinedAdministrativeActivity
start of on-study period
bridg:DefinedAdministrativeActivity
end of on-study period
bridg:DefinedAdministrativeActivity
obtain informed consent
bridg:DefinedAdministrativeActivity
verify eligibility criteria
bridg:DefinedAdministrativeActivity
enroll
bridg:DefinedAdministrativeActivity
randomize
bridg:DefinedAdministrativeActivity
complete study visits
bridg:DefinedAdministrativeActivity
exit trial
bridg:DefinedAdministrativeActivity
break treatment blind
bridg:DefinedAdministrativeActivity
protocol violation
bridg:DefinedAdministrativeActivity
premature withdrawal
bridg:DefinedAdministrativeActivity
urn:CTRv1.0:DefinedAdministrativeActivity
bridg:DefinedAdverseEvent
DefinedAdverseEvent
bridg:DefinedAdverseEvent
false
bridg:DefinedAdverseEvent
A reusable, template description of any unfavorable and unintended sign, symptom, disease, or other medical occurrence with a temporal association with the use of a medical product, procedure or other therapy, or in conjunction with a research study, regardless of causal relationship.
bridg:DefinedAdverseEvent
death
bridg:DefinedAdverseEvent
back pain
bridg:DefinedAdverseEvent
headache
bridg:DefinedAdverseEvent
pulmonary embolism
bridg:DefinedAdverseEvent
heart attack
bridg:DefinedAdverseEvent
urn:CTRv1.0:DefinedAdverseEvent
bridg:DefinedAdverseEvent
urn:SDTM_IGv3.1.2:AE.AEOCCUR
bridg:DefinedCompositionRelationship
DefinedCompositionRelationship
bridg:DefinedCompositionRelationship
false
bridg:DefinedCompositionRelationship
A relationship between a composite activity and a component activity that comprises it, i.e. parent and child activities, where all these activities are part of a global library of activities.
bridg:DefinedCompositionRelationship
A battery of tests may be composed of multiple routine labs that are always ordered together as a group.
bridg:DefinedCompositionRelationship
A glucose tolerance test which is comprised of administering glucose and taking multiple timed blood samples which are then tested for glucose.
bridg:DefinedCompositionRelationship
This class helps represent an AND relationship between siblings with the same parent activity.
bridg:DefinedCompositionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:DefinedCompositionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:DefinedCompositionRelationship
urn:CTRv1.0:DefinedCompositionRelationship
in R_Product
bridg:DefinedCompositionRelationship
urn:ICSRr2:Component
bridg:DefinedCompositionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:DefinedCompositionRelationship
urn:TDM:TriggeringRule
bridg:DefinedContingentOnRelationship
DefinedContingentOnRelationship
bridg:DefinedContingentOnRelationship
false
bridg:DefinedContingentOnRelationship
A relationship between an activity and some criteria to determine if the activity should occur where all activities are part of the global library of activities.
bridg:DefinedContingentOnRelationship
Only perform a certain lab test if drug X was administered. (target = another activity)
bridg:DefinedContingentOnRelationship
Only perform a substance administration of drug X if the blood pressure was over some threshold number. (target = observation result from another activity that is an observation)
bridg:DefinedContingentOnRelationship
Only perform a substance administration of drug Y if the blood pressure was over some threshold number and either the result of a certain lab test was positive or the subject's temperature was elevated
bridg:DefinedContingentOnRelationship
i.e. "(A and (B or C))".
bridg:DefinedContingentOnRelationship
The criteria to evaluation the relationship could be one of the following:
- the outcome of another activity where the source activity does not occur unless the target activity outcome has occurred
- another activity where the source activity does not occur unless the target activity has occurred
- a group of other criteria that may be composed of a mix of other activities, observation results and/or other groups.
To evaluate whether the contingency was satisfied, the simple existence of a PerformedActivity (or subclass) related to the DefinedActivity (or subclass) is not enough by itself. The PerformedActivity.statusCode and PerformedActivity.negationIndicator must also be checked to ensure that the activity was actually performed. PerformedActivity.statusCode must be "Completed" and PerformedActivity.negationIndicator must not be "true".
be contingent upon Exclusive Or
bridg:DefinedContingentOnRelationship
A DefinedContingentOnRelationship must be associated to one and only one of the following: DefinedActivity, DefinedObservationResult, DefinedCriterionGroup.
completionRequiredIndicator Qualifier
bridg:DefinedContingentOnRelationship
completionRequiredBeforeStartingIndicator may only be used if the target of this relationship is an activity, not if the target is an observation result or a criterion group.
bridg:DefinedContingentOnRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:DefinedContingentOnRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:DefinedContingentOnRelationship
urn:CTRv1.0:DefinedContingentOnRelationship
bridg:DefinedContingentOnRelationship
urn:HL7SD:EligibilityCriterion.Precondition2
bridg:DefinedContingentOnRelationship
urn:TDM:TriggeringRule
bridg:DefinedContingentOnRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:DefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedCriterionGroup
false
bridg:DefinedCriterionGroup
A collection of conditions joined together via composition (ANDed) and/or optionality (ORed) to form a logical expression upon which the execution of an activity is based or upon which the cessation of a repeated activity is based, where components of the group may include other activities, observation results and/or other criterion groups, and where both the criterion group and it's components are defined as part of the global library.
bridg:DefinedCriterionGroup
(A and (B or C))
bridg:DefinedCriterionGroup
where A might be an activity
bridg:DefinedCriterionGroup
B and C might be 2 different observation results
bridg:DefinedCriterionGroup
and the two sets of parentheses are 2 criterion groups
bridg:DefinedCriterionGroup
one inside (a component of) the other.
bridg:DefinedCriterionGroup
A criterion group represents the parentheses around a set of criteria in a logical expression.
bridg:DefinedCriterionGroup
urn:CTRv1.0:DefinedCriterionGroup
bridg:DefinedCriterionGroup
urn:TDMv2:DefinedCriterionGroup
bridg:DefinedCriterionGroupCompositionRelationship
DefinedCriterionGroupCompositionRelationship
bridg:DefinedCriterionGroupCompositionRelationship
false
bridg:DefinedCriterionGroupCompositionRelationship
A relationship between a criterion group and an activity, observation result or other criterion group that is a component of the group, i.e. a relationship between a logical set of parenthesis and one of the items inside the parentheses, where the criterion group and its components are both part of a global library of activities.
bridg:DefinedCriterionGroupCompositionRelationship
A battery of tests may be composed of multiple routine labs that are always ordered together as a group.
bridg:DefinedCriterionGroupCompositionRelationship
A glucose tolerance test which is comprised of administering glucose and taking multiple timed blood samples which are then tested for glucose.
bridg:DefinedCriterionGroupCompositionRelationship
This class helps represent an AND relationship between siblings in the same criterion group.
is the component of Exclusive Or
bridg:DefinedCriterionGroupCompositionRelationship
A DefinedCriterionGroupCompositionRelationship must be associated to one and only one of the following targets: DefinedActivity, DefinedObservationResult, DefinedCriterionGroup.
bridg:DefinedCriterionGroupCompositionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:DefinedCriterionGroupCompositionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:DefinedCriterionGroupCompositionRelationship
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship
bridg:DefinedCriterionGroupCompositionRelationship
urn:TDM:TriggeringRule
bridg:DefinedCriterionGroupCompositionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:DefinedCriterionGroupOptionRelationship
DefinedCriterionGroupOptionRelationship
bridg:DefinedCriterionGroupOptionRelationship
false
bridg:DefinedCriterionGroupOptionRelationship
A relationship between a criterion group and an option that can satisfy it, either an activity, observation result or other criterion group, i.e. a relationship between a logical set of parenthesis and one of the options inside the parentheses, where the criterion group and its option are both part of a global library of activities.
bridg:DefinedCriterionGroupOptionRelationship
A pain management criterion group may be comprised of three options
bridg:DefinedCriterionGroupOptionRelationship
one for substance administration of Tylenol
bridg:DefinedCriterionGroupOptionRelationship
another for substance administration of aspirin
bridg:DefinedCriterionGroupOptionRelationship
and a third for substance administration of ibuprofen. The pain management criterion would be satisfied/accomplished with any one of these activities and would be associated to each of the three via a different DefinedCriterionGroupOptionRelationship.
bridg:DefinedCriterionGroupOptionRelationship
This class helps represent an OR relationship between siblings in the same criterion group.
be the choice that has as option Exclusive Or
bridg:DefinedCriterionGroupOptionRelationship
A DefinedCriterionGroupOptionRelationship must be associated to one and only one of the following targets: DefinedActivity, DefinedObservationResult, DefinedCriterionGroup.
bridg:DefinedCriterionGroupOptionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:DefinedCriterionGroupOptionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:DefinedCriterionGroupOptionRelationship
urn:CTRv1.0:DefinedCriterionGroupOptionRelationship
bridg:DefinedCriterionGroupOptionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:DefinedCriterionGroupOptionRelationship
urn:TDM:TriggeringRule
bridg:DefinedEligibilityCriterion
DefinedEligibilityCriterion
bridg:DefinedEligibilityCriterion
false
bridg:DefinedEligibilityCriterion
An activity defined at a global library level that identifies one of a set of conditions that a subject must meet in order to participate in a study, or that a study subject must meet into order to participate in a certain part of the study.
be participated in by Qualifier
bridg:DefinedEligibilityCriterion
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:DefinedEligibilityCriterion
urn:C3PRv2.9:EligibilityCriteria.questionText
bridg:DefinedEligibilityCriterion
urn:CTRRr3:DefinedEligibilityCriterion
bridg:DefinedEligibilityCriterion
urn:CTRv1.0:DefinedEligibilityCriterion
bridg:DefinedEligibilityCriterion
urn:HL7SD:EligibilityCriterion
bridg:DefinedEligibilityCriterionAnswer
DefinedEligibilityCriterionAnswer
bridg:DefinedEligibilityCriterionAnswer
false
bridg:DefinedEligibilityCriterionAnswer
A reusable, "template" description of an allowable response to an eligibility criterion question.
bridg:DefinedExclusionCriterion
DefinedExclusionCriterion
bridg:DefinedExclusionCriterion
false
bridg:DefinedExclusionCriterion
An activity defined at a global library level that identifies a characteristic or requirement intended to be applied to a potential study subject to determine whether they may not participate in a study.
bridg:DefinedExclusionCriterion
Must be over the age of 18.
bridg:DefinedExclusionCriterion
urn:CTRRr3:DefinedExclusionCriterion
bridg:DefinedExclusionCriterion
urn:CTRv1.0:DefinedExclusionCriterion
bridg:DefinedExperimentalUnitAllocation
DefinedExperimentalUnitAllocation
bridg:DefinedExperimentalUnitAllocation
false
bridg:DefinedExperimentalUnitAllocation
An administrative activity defined at a global library level that is the assignment of an experimental unit to a portion of the study, such as an arm or a portion of an arm (when secondary allocations may occur).
bridg:DefinedExperimentalUnitAllocation
randomization
bridg:DefinedExperimentalUnitAllocation
direct assignment based on eligibility criteria
bridg:DefinedExperimentalUnitAllocation
etc.
bridg:DefinedExperimentalUnitAllocation
"Escalating dose cohort studies" enroll subjects in successive arms
bridg:DefinedExperimentalUnitAllocation
i.e.
bridg:DefinedExperimentalUnitAllocation
one arm is completely filled before any subjects are enrolled in the next arm. In such a study
bridg:DefinedExperimentalUnitAllocation
allocation depends on which arms have been fully enrolled and which are currently open for enrollment. Note that this example assumes that the experimental unit is the subject (rather than a part of a subject or a group of subjects).
Repeat Not Applicable
bridg:DefinedExperimentalUnitAllocation
The Repeat attributes should not be used for a DefinedExperimentalUnitAllocation.
be participated in by Qualifier
bridg:DefinedExperimentalUnitAllocation
Associations from ExperimentalUnit are valid. Associations from Subject (including StudySubject) are not valid.
bridg:DefinedExperimentalUnitAllocation
urn:C3PR:Randomization
bridg:DefinedExperimentalUnitAllocation
urn:CTRv1.0:DefinedExperimentalUnitAllocation
bridg:DefinedExpressionVariableRelationship
DefinedExpressionVariableRelationship
bridg:DefinedExpressionVariableRelationship
false
bridg:DefinedExpressionVariableRelationship
A relationship between a DefinedSubstanceAdministration and a DefinedObservation that identifies a factor used in a relative dose expression to calculate an absolute dose.
bridg:DefinedExpressionVariableRelationship
Relationship of a calculated dose on a substance administration and a weight observation.
bridg:DefinedExpressionVariableRelationship
Relationship of a calculated dose on a substance administration and a body surface area observation.
bridg:DefinedExpressionVariableRelationship
Formulas are used for direct mathematical calculations. Conditional assertions make use of the DefinedContingentOnRelationship class.
bridg:DefinedExpressionVariableRelationship
urn:CTRv1.0:DefinedExpressionVariableRelationship
bridg:DefinedImaging
DefinedImaging
bridg:DefinedImaging
false
bridg:DefinedImaging
An activity defined at the global library level whose intention is to obtain pictures of the interior or exterior of the body usually for diagnostic reasons.
bridg:DefinedImaging
X-ray
bridg:DefinedImaging
MRI
be participated in by Qualifier
bridg:DefinedImaging
Associations from Subject (including StudySubjects) and ExperimentalUnit are valid for BiologicEntity, BiologicEntityGroup, BiologicEntityPart, and Specimen, not for Product, ProductGroup, Organization or HealthcareFacility.
bridg:DefinedImaging
urn:CTRv1.0:DefinedImaging
bridg:DefinedInclusionCriterion
DefinedInclusionCriterion
bridg:DefinedInclusionCriterion
false
bridg:DefinedInclusionCriterion
An activity defined at a global library level that identifies a characteristic or requirement intended to be applied to a potential study subject to determine whether they may participate in a study.
bridg:DefinedInclusionCriterion
pregnancy
bridg:DefinedInclusionCriterion
urn:CTRRr3:DefinedInclusionCriterion
bridg:DefinedInclusionCriterion
urn:CTRv1.0:DefinedInclusionCriterion
bridg:DefinedMaterialProcessStep
DefinedMaterialProcessStep
bridg:DefinedMaterialProcessStep
false
bridg:DefinedMaterialProcessStep
An activity defined at a global library level that is an action of processing a material.
bridg:DefinedMaterialProcessStep
freezing
bridg:DefinedMaterialProcessStep
thawing
bridg:DefinedMaterialProcessStep
spinning
bridg:DefinedMaterialProcessStep
embedding
bridg:DefinedMaterialProcessStep
dividing
bridg:DefinedMaterialProcessStep
aliquot
bridg:DefinedMaterialProcessStep
adding additives or growth factors
bridg:DefinedMaterialProcessStep
product manipulation
bridg:DefinedMaterialProcessStep
Material process may be performed on any kind of material, such as a specimen, nanomaterial, or biologic. The result of the process may a similar or different kind of material, for instance a specimen may be the result of a specimen processing step (e.g., aliquot or division of a specimen), or alternatively a blood product has anticoagulants added to it to preserve the product. Other processsing steps, such as adding growth factor to induce cell growth, may be performed on the blood product.
bridg:DefinedMaterialStorage
DefinedMaterialStorage
bridg:DefinedMaterialStorage
false
bridg:DefinedMaterialStorage
An administrative activity defined at a global library level that is an action of safekeeping harvested material in a repository or depository.
bridg:DefinedMaterialStorage
refrigeration
bridg:DefinedMaterialStorage
cryopreservation
bridg:DefinedMaterialStorage
dehydration
bridg:DefinedMaterialStorage
There is a difference between the act of changing the state of material, which is represented by DefinedMaterialProcessStep, and the act of maintaining state of the material by storing it, which is represented by DefinedMaterialStorage.
be participated in by Qualifier
bridg:DefinedMaterialStorage
Associations from Subject (including StudySubject) and ExperimentalUnit are valid for Specimen and Product, not for BiologicEntity, BIologicEntityPart, BiologicEntityGroup, ProductGroup, HealthcareFacility or Organization.
bridg:DefinedMedicalConditionResult
DefinedMedicalConditionResult
bridg:DefinedMedicalConditionResult
false
bridg:DefinedMedicalConditionResult
A reusable template description of a sign, symptom, disease, or other medical occurrence.
bridg:DefinedMedicalConditionResult
death
bridg:DefinedMedicalConditionResult
back pain
bridg:DefinedMedicalConditionResult
headache
bridg:DefinedMedicalConditionResult
pulmonary embolism
bridg:DefinedMedicalConditionResult
heart attack
bridg:DefinedMedicalConditionResult
pregnancy
bridg:DefinedMedicalConditionResult
flu
bridg:DefinedMedicalConditionResult
broken bone
bridg:DefinedMedicalConditionResult
menstrual period
bridg:DefinedMedicalConditionResult
depression
bridg:DefinedMedicalConditionResult
Clinical Events
bridg:DefinedMedicalConditionResult
Medical History
bridg:DefinedMedicalConditionResult
urn:CTRv1.0:DefinedMedicalConditionResult
bridg:DefinedNotification
DefinedNotification
bridg:DefinedNotification
false
bridg:DefinedNotification
An administrative activity defined at the global library level that represents the communication of a message to a recipient.
bridg:DefinedNotification
An alert sent to a study PI that the study has reached 75% of target subject accrual.
be participated in by Qualifier
bridg:DefinedNotification
Associations from Subject (including StudySubject) are valid. Associations from ExperimentalUnit are not valid.
be received by actualIndicator Qualifier
bridg:DefinedNotification
Only Organization or Person (via NotificationReceiver) with actualIndicator = "false" is valid.
bridg:DefinedNotification
urn:caAERSv2.2:PlannedNotification
bridg:DefinedNotification
urn:caAERSv2.2:PlannedEmailNotification
bridg:DefinedObservation
DefinedObservation
bridg:DefinedObservation
false
bridg:DefinedObservation
An activity defined at a global library level whose intention is to obtain a result by observing, monitoring, measuring or otherwise qualitatively or quantitatively gathering data or information about one or more aspects of a subject's, study subject's or experimental unit's physiologic or psychologic state.
bridg:DefinedObservation
blood chemistry panel
bridg:DefinedObservation
body mass index calculation
bridg:DefinedObservation
blood pressure measurement
bridg:DefinedObservation
urn:CTRPv3.8:PlannedObservation
bridg:DefinedObservation
urn:CTRRr3:DefinedObservation
bridg:DefinedObservation
urn:CTRv1.0:DefinedObservation
bridg:DefinedObservationResult
DefinedObservationResult
bridg:DefinedObservationResult
false
bridg:DefinedObservationResult
A reusable, "template" description of possible findings of an observation.
bridg:DefinedObservationResult
A blood pressure measurement may result in a diastolic number and a systolic number.
bridg:DefinedObservationResult
The DefinedObservationResult class can be used to represent defined ranges for contingencies by constraining the result attribute from ANY to IVL<PQ>, for instance, or any other range value. Such DefinedObservationResults may be used as criteria for conditional activities or repeated activities.
bridg:DefinedObservationResult
urn:CTRRr3:DefinedObservationResult
bridg:DefinedObservationResult
urn:CTRv1.0:DefinedObservationResult
bridg:DefinedOptionRelationship
DefinedOptionRelationship
bridg:DefinedOptionRelationship
false
bridg:DefinedOptionRelationship
A relationship between a composite activity and an option that can satisfy it, i.e. choice and option activities, where all these activities are part of a global library of activities.
bridg:DefinedOptionRelationship
A pain management activity may be comprised of three options
bridg:DefinedOptionRelationship
one for substance administration of Tylenol
bridg:DefinedOptionRelationship
another for substance administration of aspirin
bridg:DefinedOptionRelationship
and a third for substance administration of ibuprofen. The pain management activity would be satisfied/accomplished with any one of these activities and would be associated to each of the three via a different DefinedOptionRelationship.
bridg:DefinedOptionRelationship
This class helps represent an OR relationship between siblings with the same parent activity.
bridg:DefinedOptionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:DefinedOptionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:DefinedOptionRelationship
urn:CTRv1.0:DefinedOptionRelationship
bridg:DefinedOptionRelationship
urn:TDM:TriggeringRule
bridg:DefinedOptionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:DefinedProcedure
DefinedProcedure
bridg:DefinedProcedure
false
bridg:DefinedProcedure
An activity defined at a global library level that is an action whose immediate and primary intention is the alteration of the physical condition of the subject, study subject or experimental unit.
bridg:DefinedProcedure
Procedures may involve the disruption of some body surface (e.g. an incision in a surgical procedure).
bridg:DefinedProcedure
Conservative procedures such as reduction of a luxated joint
bridg:DefinedProcedure
including physiotherapy such as chiropractic treatment
bridg:DefinedProcedure
massage
bridg:DefinedProcedure
balneotherapy
bridg:DefinedProcedure
acupuncture
bridg:DefinedProcedure
shiatsu.
use actualIndicator Qualifier
bridg:DefinedProcedure
Only Product with actualIndicator = “false” is valid.
bridg:DefinedProcedure
urn:CTRPv3.8:PlannedProcedure
bridg:DefinedProcedure
urn:CTRR:Intervention_Name
bridg:DefinedProcedure
urn:CTRRr3:DefinedProcedure
bridg:DefinedProcedure
urn:CTRv1.0:DefinedProcedure
bridg:DefinedRepeatActivityUntilRule
DefinedRepeatActivityUntilRule
bridg:DefinedRepeatActivityUntilRule
false
bridg:DefinedRepeatActivityUntilRule
A relationship between a defined repeating activity and the criteria that may trigger the repeating activity to stop, where all items are part of a global library.
bridg:DefinedRepeatActivityUntilRule
Continue repeating kidney dialysis until kidney transplant surgery. Continue performing a certain lab test weekly until the three-month checkup occurs. (target = another activity) Continue substance administration of drug X until the blood pressure is over some minimum threshold number. (target = observation result from another activity that is an observation) Continue substance administration of drug Y until the blood pressure is over some minimum threshold number and either the result of a certain lab test is positive or the subject's temperature is elevated
bridg:DefinedRepeatActivityUntilRule
i.e. "(A and (B or C))".
bridg:DefinedRepeatActivityUntilRule
The criteria to stop the repeating activity by be one of the following:
- another defined activity where the repeating activity stops if this other activity occurs
- a defined observation result where the repeating activity stops if this observation result occurs
- a defined criteria group where the repeating activity stops if this group logically evaluates to true based on its components
be repeated until Exclusive Or
bridg:DefinedRepeatActivityUntilRule
A DefinedRepeatActivityUntilRule must be associated to one and only one of the following: DefinedActivity, DefinedObservationResult, DefinedCriterionGroup.
bridg:DefinedRepeatActivityUntilRule
urn:CTOM:ActivityRelationship.typeCode
bridg:DefinedRepeatActivityUntilRule
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:DefinedRepeatActivityUntilRule
urn:CTRv1.0:DefinedRepeatActivityUntilRule
bridg:DefinedRepeatActivityUntilRule
urn:TDM:TriggeringRule
bridg:DefinedRepeatActivityUntilRule
urn:TDM:AbstractRule.evaluableExpression
bridg:DefinedSpecimenCollection
DefinedSpecimenCollection
bridg:DefinedSpecimenCollection
false
bridg:DefinedSpecimenCollection
An activity defined at a global library level that is an action of gathering samples that may be used for subsequent analysis.
bridg:DefinedSpecimenCollection
blood draw
results in actualIndicator Qualifier
bridg:DefinedSpecimenCollection
Only Material (via Specimen) with actualIndicator = “false” is valid.
bridg:DefinedSpecimenCollection
urn:BRIDGSCC:Model_Integrity
bridg:DefinedSpecimenCollection
urn:CTRv1.0:DefinedSpecimenCollection
bridg:DefinedStratificationCriterion
DefinedStratificationCriterion
bridg:DefinedStratificationCriterion
false
bridg:DefinedStratificationCriterion
An activity defined at a global library level that identifies pre-treatment factors by which study subjects are segregated to assure balance of these factors during analysis or before randomization to a study arm or some smaller segment of a study. The decisive factor used to help segregate the study subject into a stratum group for analysis or randomization purposes.
Permissible Result Qualifier
bridg:DefinedStratificationCriterion
A DefinedStratificationCriterion must be associated with 2 or more DefinedStratificationCriterionPermissibleResults.
be participated in by Qualifier
bridg:DefinedStratificationCriterion
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:DefinedStratificationCriterion
urn:C3PRv2.9:StratificationCriterion
bridg:DefinedStratificationCriterion
urn:CTRv1.0:DefinedStratificationCriterion
bridg:DefinedStratificationCriterion
urn:NCI_CRF_Standard:CDE_3608v4.0:_Study_Stratification_Text
bridg:DefinedStratificationCriterionPermissibleResult
DefinedStratificationCriterionPermissibleResult
bridg:DefinedStratificationCriterionPermissibleResult
false
bridg:DefinedStratificationCriterionPermissibleResult
A reusable, "template" description of an allowable response to a stratification criterion.
bridg:DefinedStratificationCriterionPermissibleResult
The stratification criterion for gender can have permissible answers of male and female
Association Cardinality Qualifier
bridg:DefinedStratificationCriterionPermissibleResult
For associations between DefinedStratificationCriterion and DefinedStratificationCriterionPermissibleResult (via DefinedObservation and DefinedObservationResult), the cardinality should be 2..* on the DefinedStratificationCriterionPermissibleResult.
bridg:DefinedStratificationCriterionPermissibleResult
urn:C3PRv2.9:StratificationCriterionAnswerCombination
bridg:DefinedStratificationCriterionPermissibleResult
urn:C3PRv2.9:StratificationCriterionPermissibleAnswer
bridg:DefinedStratificationCriterionPermissibleResult
urn:CTRv1.0:DefinedStratificationCriterionPermissibleResult
bridg:DefinedStudyAdministrativeActivity
DefinedStudyAdministrativeActivity
bridg:DefinedStudyAdministrativeActivity
false
bridg:DefinedStudyAdministrativeActivity
An administrative activity defined at a global library level that is independent of a study subject but is necessary for the conduct of the study.
bridg:DefinedStudyAdministrativeActivity
IRB Approval
bridg:DefinedStudyAdministrativeActivity
site enrollment
bridg:DefinedStudyAdministrativeActivity
FDA audit
be participated in by Not Applicable
bridg:DefinedStudyAdministrativeActivity
Associations from Subject (including StudySubject) and ExperimentalUnit are not valid.
bridg:DefinedStudyAdministrativeActivity
urn:CTRv1.0:DefinedStudyAdministrativeActivity
bridg:DefinedStudyAgentTransfer
DefinedStudyAgentTransfer
bridg:DefinedStudyAgentTransfer
false
bridg:DefinedStudyAgentTransfer
An administrative activity defined at a global library level that is an action in which an authorized party at a designated study site dispenses or receives a study agent to/from a study subject, though as a defined activity, no actual study subject is identified.
bridg:DefinedStudyAgentTransfer
Dispensing a bottle of pills
bridg:DefinedStudyAgentTransfer
The term "study agent" only pertains within the context of a given study. To make this explicit in BRIDG it was determined that the StudyAgent class would only be used to connect Product to StudyProtocolVersion. All activity-related classes would be associated directly to Product to avoid the issues of activities that may cross study boundaries. To determine if a given activity uses a study agent one need only compare the product used in the activity with the list of products associated to StudyAgent for a given StudyProtocolVersion. It should be noted that this determination could be different for different studies and could evolve over the course of a given study.
be participated in by Qualifier
bridg:DefinedStudyAgentTransfer
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
is a transfer of Qualifier
bridg:DefinedStudyAgentTransfer
Associations from Product are valid only for Products that are associated to StudyAgent with the same StudyProtocolVersion as the StudyProtocolVersion associated to the DefinedStudyAgentTransfer.
is a transfer of actualIndicator Qualifier
bridg:DefinedStudyAgentTransfer
Only Product with actualIndicator = "false" is valid.
bridg:DefinedStudySubjectMilestone
DefinedStudySubjectMilestone
bridg:DefinedStudySubjectMilestone
false
bridg:DefinedStudySubjectMilestone
An administrative activity defined at a global library level that represents a common administrative landmark for a study subject in the course of a study.
bridg:DefinedStudySubjectMilestone
obtain informed consent
bridg:DefinedStudySubjectMilestone
verify eligibility criteria
bridg:DefinedStudySubjectMilestone
enroll
bridg:DefinedStudySubjectMilestone
registration to a study
bridg:DefinedStudySubjectMilestone
randomize
bridg:DefinedStudySubjectMilestone
assignment to a treatment arm
bridg:DefinedStudySubjectMilestone
start of on-study period
bridg:DefinedStudySubjectMilestone
complete study visits
bridg:DefinedStudySubjectMilestone
end of on-study period
bridg:DefinedStudySubjectMilestone
exit trial
bridg:DefinedStudySubjectMilestone
break treatment blind
bridg:DefinedStudySubjectMilestone
protocol violation
bridg:DefinedStudySubjectMilestone
premature withdrawal
be participated in by Qualifier
bridg:DefinedStudySubjectMilestone
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:DefinedStudySubjectMilestone
urn:C3PRv2.9:ScheduledEpoch.scEpochWorkflowStatus
bridg:DefinedStudySubjectMilestone
urn:CTRv1.0:DefinedStudySubjectMilestone
bridg:DefinedSubjectActivityGroup
DefinedSubjectActivityGroup
bridg:DefinedSubjectActivityGroup
false
bridg:DefinedSubjectActivityGroup
A collection of activities from a global library that would be performed on a common study subject.
bridg:DefinedSubjectActivityGroup
Clinic visit during which a physical exam
bridg:DefinedSubjectActivityGroup
a blood test
bridg:DefinedSubjectActivityGroup
and a substance administration occur
bridg:DefinedSubjectActivityGroup
Telephone contact during which temperature
bridg:DefinedSubjectActivityGroup
blood pressure and adverse events are reported
bridg:DefinedSubjectActivityGroup
Recording multiple observation results in a diary
bridg:DefinedSubjectActivityGroup
A treatment strategy that consists of drug administrations with rules for modifying doses
bridg:DefinedSubjectActivityGroup
study segment
bridg:DefinedSubjectActivityGroup
course
bridg:DefinedSubjectActivityGroup
treatment strategy
bridg:DefinedSubjectActivityGroup
period
bridg:DefinedSubjectActivityGroup
cycle
be participated in by Qualifier
bridg:DefinedSubjectActivityGroup
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:DefinedSubjectActivityGroup
urn:C3PRv2.9:Arm.name
bridg:DefinedSubjectActivityGroup
urn:CTRv1.0:DefinedSubjectActivityGroup
bridg:DefinedSubjectActivityGroup
urn:caAERSv2.2:Arm
bridg:DefinedSubjectActivityGroup
urn:caAERSv2.2:TreatmentAssignment
bridg:DefinedSubstanceAdministration
DefinedSubstanceAdministration
bridg:DefinedSubstanceAdministration
false
bridg:DefinedSubstanceAdministration
An activity defined at a global library level that is an action of applying, introducing or otherwise giving medications or other substances to a subject or experimental unit.
bridg:DefinedSubstanceAdministration
Administration of methotrexate as part of chemotherapy.
Dose Expression Qualifier
bridg:DefinedSubstanceAdministration
If a dose expression uses parameters, each parameter must be defined as a DefinedExpressionVariableRelationship.localVariableName.
Dose Qualifier
bridg:DefinedSubstanceAdministration
productDose, periodProductDoseTotal must only be used when the DefinedSubstanceAdministration is associated to a single Product. Otherwise, it would be ambiguous to which Product the amounts indicated in these attributes apply.
be participated in by Qualifier
bridg:DefinedSubstanceAdministration
Associations from Subject (including StudySubject) are valid only for BiologicEntity, BiologicEntityGroup and Specimen, not for Product, HealthcareFacility or Organization. Associations from ExperimentalUnit are valid for BiologicEntity, BiologicEntityGroup, BiologicEntityPart and Specimen, but not for Product or ProductGroup.
bridg:DefinedSubstanceAdministration
urn:CTRPv3.8:PlannedSubstanceAdministration
bridg:DefinedSubstanceAdministration
urn:CTRRr3:DefinedSubstanceAdministration
bridg:DefinedSubstanceAdministration
urn:CTRv1.0:DefinedSubstanceAdministration
bridg:Device
Device
bridg:Device
false
bridg:Device
An object intended for use whether alone or in combination for diagnostic, prevention, monitoring, therapeutic, scientific, and/or experimental purposes.
bridg:Device
tongue depressor
bridg:Device
pacemaker
bridg:Device
insulin pump
bridg:Device
EKG machine
bridg:Device
x-ray machine
bridg:Device
mass spectrometer
bridg:Device
polymerase chain reaction (PCR) machine
bridg:Device
microscope
bridg:Device
pH meter
Attribute Set actualIndicator Qualifier
bridg:Device
effectiveDateRange, codeModifiedText, lotNumberText, expirationDate, manufactureDate, returnedToReprocessorDate are valid only when actualIndicator = "true".
bridg:Device
urn:AE:Device
bridg:Device
urn:CTRPv1.0:Device
bridg:Device
urn:CTRRr3:Device
bridg:Device
urn:CTRv1.0:Device
in R_Product
bridg:Device
urn:ICSRr2:DeviceInstance
bridg:Device
urn:caAERSv2.2:MedicalDevice
bridg:Distributor
Distributor
bridg:Distributor
false
bridg:Distributor
An organization who takes part in the distribution chain for a product, as it is moved from its producer to the ultimate consumer.
bridg:Distributor
urn:AE:Distributor
bridg:Document
Document
bridg:Document
false
bridg:Document
An organized representation of information in publishable, human-readable form (that persists over time).
bridg:Document
Study Protocol
bridg:Document
Adverse Event Report
bridg:Document
Expedited Adverse Event Report
bridg:Document
Institutional Review Board (IRB) Report
bridg:Document
X-Ray Report
bridg:Document
Lab Summary Report
bridg:Document
Autopsy Report
bridg:Document
A document groups the various document versions and has the following characteristics: 1) Stewardship, 2) Potential for authentication, 3) Wholeness, 4) Human readability, 5) Persistence, 6) Global vs local context (the person that signs it is the author of all sections unless otherwise noted).
Regulatory processes require the submission of documents from the Applicant to the Regulatory Authority. These documents are varied in focus and are often defined by the field of study or by the regulatory application requirements of the region or Regulatory Authority (e.g., Integrated Summary of Safety, Pharmacokinetics Written Summary).
bridg:Document
urn:AE:Document
bridg:Document
urn:C3PRv2.9:Consent
bridg:Document
urn:CTRPv1.0:Document
bridg:Document
urn:CTRPv3.8:Document
bridg:Document
urn:CTRR:Protocol_Title
bridg:Document
urn:CTRv1.0:Document
in IndividualCaseSafetyReport
bridg:Document
urn:ICSRr2:document
bridg:Document
urn:RPS1:Documentation
bridg:Document
urn:Statistics_v1.0:Document
bridg:DocumentAuthor
DocumentAuthor
bridg:DocumentAuthor
false
bridg:DocumentAuthor
The individual who is responsible for the content of a document.
bridg:DocumentAuthor
A healthcare provider could be the author of a study protocol document
Performer Document Pair Unique
bridg:DocumentAuthor
Each DocumentVersion can have more than one DocumentAuthor but each of them must be a different ResearchStaff, Subject, AssociatedBiologicEntity, or HealthcareProvider (no duplicate Person/ResearchOrganization pairs).
Study Author performed by Qualifier
bridg:DocumentAuthor
When the DocumentAuthor is an author for a StudyProtocolDocumentVersion, the DocumentAuthor must be a function performed by a HealthcareProvider or ResearchStaff only.
be a function performed by Exclusive Or
bridg:DocumentAuthor
A DocumentAuthor is a function performed by one and only one of the following: ResearchStaff, Subject, AssociatedBiologicEntity, HealthcareProvider.
be a function performed by Qualifier
bridg:DocumentAuthor
The DocumentAuthor must be a function performed by a Subject who is a Person and not an Animal or Product or Specimen.
bridg:DocumentAuthor
urn:AE:Reporter
bridg:DocumentAuthor
urn:CTRv1.0:DocumentAuthor
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:LocatedEntity2
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:Participant2
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:AssignedEntity
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:LocatedEntity
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:Participant1
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:Author3
in IndividualCaseSafetyReport
bridg:DocumentAuthor
urn:ICSRr2:AssignedEntity.code
bridg:DocumentAuthor
urn:caAERSv2.2:RoleBasedRecipient.role
bridg:DocumentAuthor
urn:caAERSv2.2:Reporter
bridg:DocumentAuthor
urn:caAERSv2.2:Physician
bridg:DocumentIdentifier
DocumentIdentifier
bridg:DocumentIdentifier
false
bridg:DocumentIdentifier
The unique identification of a document in a specified context.
bridg:DocumentIdentifier
In context of a study protocol document
bridg:DocumentIdentifier
document identifiers are the various unique identifiers assigned to a study by different organizations.
bridg:DocumentIdentifier
This class is a resolution of the requirement for noting the type of an identifier which is not handled by the purely technical HL7 II data type.
bridg:DocumentIdentifier
NOTE: Until further clarification, the BRIDG SCC believes the IND/IDE regulatory application serial number is the number assigned by the applicant/sponsor to a document that is either a supplement or an amendment to the original submission unit and is represented using DocumentIdentifier.identifer.
bridg:DocumentIdentifier
NOTE: Until further clarification, the BRIDG SCC believes the IND/IDE regulatory application serial number is the number assigned by the applicant/sponsor to a document that is either a supplement or an amendment to the original submission unit and is represented using DocumentIdentifier.identifer.
be assigned by Exclusive Or
bridg:DocumentIdentifier
A DocumentIdentifier is assigned by one and only one of the following: Organization, StudyRegistry, SystemOfRecord.
be assigned by actualIndicator Qualifier
bridg:DocumentIdentifier
Only Organization with actualIndicator = "true" is valid.
bridg:DocumentIdentifier
urn:CTRRr3:DocumentIdentifier
bridg:DocumentIdentifier
urn:CTRv1.0:DocumentIdentifier
bridg:DocumentIdentifier
urn:HL7SP:DocumentIdentifier
in IndividualCaseSafetyReport
bridg:DocumentIdentifier
urn:ICSRr2:Authorization
in IndividualCaseSafetyReport
bridg:DocumentIdentifier
urn:ICSRr2:StudyRegistration
bridg:DocumentIdentifier
urn:Statistics_v1.0:DocumentIdentifier
bridg:DocumentVersion
DocumentVersion
bridg:DocumentVersion
false
bridg:DocumentVersion
A representation of a particular edition or snapshot of a document as it exists at a particular point in time.
bridg:DocumentVersion
Version 3 of a case report form (CRF) for a physical exam
bridg:DocumentVersion
version 2 of an informed consent form.
language Qualifier
bridg:DocumentVersion
DocumentVersion.languageCode must equal DocumentVersion.text(ED).languageCode if both are non-null.
bridg:DocumentVersion
urn:C3PRv2.9:Consent
bridg:DocumentVersion
urn:C3PRv2.9:StudySubjectConsentVersion
bridg:DocumentVersion
urn:CTRRr3:Document
bridg:DocumentVersion
urn:CTRv1.0:DocumentVersion
bridg:DocumentVersion
urn:Statistics_v1.0:DocumentVersion
bridg:DocumentVersion
urn:caAERSv2.2:NotificationAttachment
bridg:DocumentVersionRelationship
DocumentVersionRelationship
bridg:DocumentVersionRelationship
false
bridg:DocumentVersionRelationship
Specifies the meaning (or semantics) of the relationship between one document version and another.
bridg:DocumentVersionRelationship
The DocumentVersions on either side of the DocumentVersionRelationship do not necessarily have to be related to the same Document, or even have the same Document.typeCode.
bridg:DocumentVersionRelationship
NOTE: BRIDG SCC acknowledges that there are two ways to represent the relationship between a study protocol and a document that is cited by the study protocol: 1) use the StudyProtocolVersion to StudyReference association; 2) use the StudyProtocolVersion > StudyProtocolDocumentVersion > DocumentVersionRelationship associations. The first is more direct and uses domain terminology, while the second is more consistent with other document-to-document associations. The SCC hopes to clarify this ambiguity in a future release when a project dealing with publications or a related area comes to harmonization.
bridg:DocumentVersionRelationship
urn:CTRPv3.8:StudyRelationship
StudyRelationship
bridg:DocumentVersionRelationship
urn:CTRPv3.8:StudyProtocol.
bridg:DocumentVersionRelationship
urn:CTRv1.0:DocumentVersionRelationship
bridg:DocumentVersionRelationship
urn:HL7SD:ReplacementOf1
in IndividualCaseSafetyReport
bridg:DocumentVersionRelationship
urn:ICSRr2:reference
in IndividualCaseSafetyReport
bridg:DocumentVersionRelationship
urn:ICSRr2:SourceOf2
in IndividualCaseSafetyReport
bridg:DocumentVersionRelationship
urn:ICSRr2:SourceOf1
bridg:DocumentVersionRelationship
urn:RPS1:RelatedDocumentation
bridg:DocumentVersionWorkflowStatus
DocumentVersionWorkflowStatus
bridg:DocumentVersionWorkflowStatus
false
bridg:DocumentVersionWorkflowStatus
The workflow status associated with a document version from submission thru abstraction.
bridg:DocumentVersionWorkflowStatus
Please refer to the Processing Status state transition diagram for further details.
bridg:DocumentVersionWorkflowStatus
urn:CTRPv1.0:DocumentWorkflowStatus
bridg:DocumentVersionWorkflowStatus
urn:CTRPv3.8:DocumentWorkflowStatus
bridg:DocumentVersionWorkflowStatus
urn:CTRv1.0:DocumentVersionWorkflowStatus
bridg:DocumentVersionWorkflowStatus
urn:RPS1:Documentation.status
bridg:DonorRegistry
DonorRegistry
bridg:DonorRegistry
false
bridg:DonorRegistry
An organization that administers the registration of donors of materials for transplantation.
bridg:DonorRegistry
'Be The Match' registry maintained by the National Marrow Donor Program (NMDP)
bridg:DonorRegistry
The registry should contain basic information about each donor sufficient to identify duplicate entries and match donors to potential recipients.
There may be names for the registry, e.g., "Be The Match", however, we do not have a requirement for adding this at this time.
bridg:Drug
Drug
bridg:Drug
false
bridg:Drug
An article other than food intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease; or intended to affect the structure or any function of the body.
bridg:Drug
aspirin
bridg:Drug
urn:CTRPv1.0:Drug
bridg:Drug
urn:CTRv1.0:Drug
bridg:Drug
urn:caAERSv2.2:ChemoAgent
bridg:Epoch
Epoch
bridg:Epoch
false
bridg:Epoch
One of a set of ordered partitions of a subject's, study subject's or experimental unit's participation in a study. An Epoch represents a state within a study such that subjects in separate arms within that state are comparable.
Each epoch serves a purpose in the study as a whole, typically exposing the subject to a treatment or preparing them for a treatment, or gathering post-treatment data. Activities and activity results control the subject's movement from one epoch to another.
bridg:Epoch
A study designed to assess the effects of treatments might have 3 epochs.
bridg:Epoch
A Screening Epoch in which subjects' eligibility is determined and baseline measurements are made.
bridg:Epoch
A Treatment Epoch during which treatments are given and effects of treatment are assessed.
bridg:Epoch
A Follow-up Epoch during which post-treatment assessments are conducted.
bridg:Epoch
A subject moves from one epoch to another and can only be in one epoch at a time. The subject can only move to an epoch with a greater sequenceNumber. Activities in the same epoch but a different arm need not be similar in time and pattern. Subjects in different arms will not necessarily pass through the same epochs.
Mandatory Attribute Qualifier
bridg:Epoch
At least one of the following attributes must be mandatory for Epoch: name, typeCode, sequenceNumber.
name Unique
bridg:Epoch
An Epoch name must be unique within the context of the study that contains it.
bridg:Epoch
urn:C3PRv2.9:Epoch
bridg:Epoch
urn:CTRPv3.8:Epoch
bridg:Epoch
urn:CTRv1.0:Epoch
bridg:Epoch
urn:PSCv2.6:Epoch
bridg:Epoch
urn:caAERSv2.2:Epoch
bridg:EvaluatedActivityRelationship
EvaluatedActivityRelationship
bridg:EvaluatedActivityRelationship
false
bridg:EvaluatedActivityRelationship
Specifies the link between an adverse event causal assessment and the activity evaluated as a possible cause.
bridg:EvaluatedActivityRelationship
Administration of cold medicine may be evaluated as a cause of an adverse event.
bridg:EvaluatedActivityRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:EvaluatedActivityRelationship
urn:CTRv1.0:EvaluatedActivityRelationship
in IndividualCaseSafetyReport
bridg:EvaluatedActivityRelationship
urn:ICSRr2:Subject3
in IndividualCaseSafetyReport
bridg:EvaluatedActivityRelationship
urn:ICSRr2:Subject11
bridg:EvaluatedActivityRelationship
urn:caAERSv2.2:AdverseEventAttribution
bridg:EvaluatedActivityRelationship
urn:caAERSv2.2:SurgeryAttribution
bridg:EvaluatedActivityRelationship
urn:caAERSv2.2:CourseAgentAttribution
bridg:EvaluatedActivityRelationship
urn:caAERSv2.2:ConcomitantMedicationAttribution
bridg:EvaluatedActivityRelationship
urn:caAERSv2.2:DeviceAttribution
bridg:EvaluatedActivityRelationship
urn:caAERSv2.2:RadiationAttribution
bridg:EvaluatedResultRelationship
EvaluatedResultRelationship
bridg:EvaluatedResultRelationship
false
bridg:EvaluatedResultRelationship
Specifies the link between an adverse event causal assessment and the observation result evaluated as a possible cause.
bridg:EvaluatedResultRelationship
A diagnosis of diabetes may be evaluated as a cause of an adverse event.
bridg:EvaluatedResultRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:EvaluatedResultRelationship
urn:CTRv1.0:EvaluatedResultRelationship
bridg:EvaluatedResultRelationship
urn:caAERSv2.2:AdverseEventAttribution
bridg:EvaluatedResultRelationship
urn:caAERSv2.2:DiseaseAttribution
bridg:ExpandedAccessStudyProtocolVersion
ExpandedAccessStudyProtocolVersion
bridg:ExpandedAccessStudyProtocolVersion
false
bridg:ExpandedAccessStudyProtocolVersion
An action plan of a pre-clinical or clinical study describing the procedure for obtaining an experimental drug or device for patients who are not adequately treated by existing therapy, who do not meet eligibility criteria for enrollment, or who are otherwise unable to participate in a controlled clinical study.
bridg:ExpandedAccessStudyProtocolVersion
This type of study is used to register all types of non-protocol access to experimental treatments, including protocol exception, single-patient IND, treatment IND, compassionate use, emergency use, continued access and parallel track. (Parallel track means there is a separate group of subjects that go through the same protocol activities but that didn't get on the main study due to different reasons such as eligibility criteria, location, etc. and their outcome data is collected and analyzed, just not analyzed with the other data, rather in parallel.)
bridg:ExpandedAccessStudyProtocolVersion
urn:CTRRr3:Study.typeCode
bridg:ExpandedAccessStudyProtocolVersion
urn:CTRv1.0:ExpandedAccessStudyProtocolVersion
bridg:ExperimentalUnit
ExperimentalUnit
bridg:ExperimentalUnit
false
bridg:ExperimentalUnit
A physical entity which is the primary unit of interest in a specific research objective.
bridg:ExperimentalUnit
If all pigs in a pen receive the same intervention in their feed
bridg:ExperimentalUnit
and the primary observations and analyses of interest are associated with the entire pen (e.g. total feed consumed
bridg:ExperimentalUnit
total weight of all pigs combined)
bridg:ExperimentalUnit
then the pen of pigs rather than the individual animal is the experimental unit. [example from the CDISC/HL7 Study Participation message]
bridg:ExperimentalUnit
A human may have 10 patches of skin each considered an experimental unit. A product may have 10 bearings in it
bridg:ExperimentalUnit
each considered an experimental unit. Alternatively
bridg:ExperimentalUnit
the whole human or product may be an experimental unit.
bridg:ExperimentalUnit
Depending on the research objectives, a single study may have multiple levels of experimental units, such as whole people and patches of skin.
In an interventional study, the experimental unit is assigned to an intervention. The experimental unit is also the unit of primary statistical analysis. Commonly the individual study subject (animal, person or product) is the experimental unit. Different experimental units must be capable of receiving different experimental interventions.
be a function performed by Exclusive Or
bridg:ExperimentalUnit
An ExperimentalUnit may be a function performed by one and only one of the following: BiologicEntityPart, BiologicEntity, BiologicEntityGroup, Product, ProductGroup, Specimen.
bridg:ExperimentalUnit
urn:CTRRr3:ExperimentalUnit
bridg:ExperimentalUnit
urn:CTRv1.0:ExperimentalUnit
bridg:ExperimentalUnit
urn:HL7SP:ExperimentalUnit
bridg:FoodProduct
FoodProduct
bridg:FoodProduct
false
bridg:FoodProduct
A substance consumed by a human or animal for nutritional purposes.
bridg:FoodProduct
broccoli
bridg:FoodProduct
donuts
bridg:FoodProduct
pet treats
bridg:FoodProduct
urn:CTRPv1.0:FoodProduct
bridg:FoodProduct
urn:CTRv1.0:FoodProduct
bridg:Funding
Funding
bridg:Funding
false
bridg:Funding
Fiscal support for research from industry, government, or non-commercial, non-governmental organizations.
bridg:Funding
Funding from pharmaceutical
bridg:Funding
device or biotechnology companies
bridg:Funding
the US NIH or the Gates Foundation.
s of Monetary or Material Support
bridg:Funding
urn:CTRR:Source
bridg:Funding
urn:caAERSv2.2:StudyFundingSponsor
bridg:GeneralStatisticalConsideration
GeneralStatisticalConsideration
bridg:GeneralStatisticalConsideration
false
bridg:GeneralStatisticalConsideration
Information needed for conducting multiple analyses.
bridg:GeneralStatisticalConsideration
Centers within a region with fewer than 3 subjects will be grouped into a pooled center for the region.
bridg:GeneralStatisticalConsideration
urn:Statistics_v1.0:
bridg:GovernmentFunding
GovernmentFunding
bridg:GovernmentFunding
false
bridg:GovernmentFunding
Fiscal support from governmental organizations.
bridg:GovernmentFunding
United States National Institutes of Health (NIH)
bridg:HealthcareFacility
HealthcareFacility
bridg:HealthcareFacility
false
bridg:HealthcareFacility
An organization that devotes some or all of its resources (people, places, things) to the delivery of healthcare services (including the financial and administrative management of those resources).
bridg:HealthcareFacility
Northwestern Memorial Hospital
bridg:HealthcareFacility
A healthcare facility may be manifest as a single physical location (e.g. building), or, alternatively, as a distributed collection of physical spaces.
bridg:HealthcareFacility
urn:C3PRv2.9:RemoteHealthcareSite
bridg:HealthcareFacility
urn:C3PRv2.9:HealthcareSite
bridg:HealthcareFacility
urn:CTRPv1.0:HealthCareFacility
bridg:HealthcareFacility
urn:CTRPv3.8:HealthCareFacility
bridg:HealthcareFacility
urn:CTRv1.0:HealthcareFacility
bridg:HealthcareFacility
urn:HL7SD:StudySite
bridg:HealthcareFacility
urn:HL7SP:StudySite
bridg:HealthcareFacility
urn:HL7SP:Site
bridg:HealthcareFacility
urn:LabViewer2.2:HealthcareSite
bridg:HealthcareFacility
urn:PSCv2.6:Site
bridg:HealthcareProvider
HealthcareProvider
bridg:HealthcareProvider
false
bridg:HealthcareProvider
A person who directly or indirectly administers interventions that are designed to improve the physical or emotional status of a biologic entity. A person licensed, certified or otherwise authorized or permitted by law to administer healthcare in the ordinary course of business or practice of a profession.
bridg:HealthcareProvider
urn:C3PRv2.9:HealthcareSiteInvestigator
bridg:HealthcareProvider
urn:C3PRv2.9:Investigator
bridg:HealthcareProvider
urn:CTRPv1.0:HealthCareProvider
bridg:HealthcareProvider
urn:CTRPv3.8:HealthCareProvider
bridg:HealthcareProvider
urn:CTRRr3:HealthcareProvider
bridg:HealthcareProvider
urn:CTRv1.0:HealthcareProvider
bridg:HealthcareProvider
urn:HL7SP:LicensedEntity
bridg:HealthcareProvider
urn:HL7SP:Investigator
bridg:HealthcareProvider
urn:LabViewer2.2:Investigator
bridg:HealthcareProvider
urn:caAERSv2.2:SiteInvestigator
bridg:HealthcareProvider
urn:caAERSv2.2:RoleBasedRecipient.role
bridg:HealthcareProvider
urn:caAERSv2.2:Investigator
bridg:HealthcareProviderGroup
HealthcareProviderGroup
bridg:HealthcareProviderGroup
false
bridg:HealthcareProviderGroup
A collection of healthcare providers loosely based upon a criterion (i.e., specialty, department, credentials).
bridg:HealthcareProviderGroup
urn:C3PRv2.9:InvestigatorGroup
bridg:HealthcareProviderGroup
urn:CoopGrp:HealthcareProviderGroup
bridg:HealthcareProviderGroupMember
HealthcareProviderGroupMember
bridg:HealthcareProviderGroupMember
false
bridg:HealthcareProviderGroupMember
The role of an individual healthcare provider as a constituent part of a group.
bridg:HealthcareProviderGroupMember
urn:C3PRv2.9:SiteInvestigatorGroupAffiliation
bridg:HealthcareProviderGroupMember
urn:CoopGrp:HealthcareProviderGroupMember
bridg:IntegratedStatisticalAnalysisPlan
IntegratedStatisticalAnalysisPlan
bridg:IntegratedStatisticalAnalysisPlan
false
bridg:IntegratedStatisticalAnalysisPlan
A type of statistical analysis plan that is intended to draw conclusions across multiple studies.
bridg:IntegratedStatisticalAnalysisPlan
Plan for integrated analysis of safety data in support of the Integrated Summary of Safety (ISS).
bridg:IntegratedStatisticalAnalysisPlan
Plan for integrated analysis of efficacy data in support of the Integrated Summary of Effectiveness (ISE).
bridg:IntegratedStatisticalAnalysisPlan
Plan for multi-study analysis to be presented in a manuscript.
bridg:IntegratedStatisticalAnalysisPlan
Plan for a meta-analysis of literature studies.
bridg:IntegratedStatisticalAnalysisPlan
urn:Statistics_v1.0:IntegratedStatisticalAnalysisPlan
bridg:InterventionalStudyProtocolVersion
InterventionalStudyProtocolVersion
bridg:InterventionalStudyProtocolVersion
false
bridg:InterventionalStudyProtocolVersion
An action plan of a pre-clinical or clinical study in which study subjects or experimental units are assigned by an investigator based on a protocol to receive specific interventions.
bridg:InterventionalStudyProtocolVersion
Study subjects or experimental units may receive diagnostic, therapeutic or other types of interventions. The assignment of the intervention may or may not be random. The study subjects or experimental units are then followed and biomedical and/or health outcomes are assessed.
blindedRoleCode Qualifier
bridg:InterventionalStudyProtocolVersion
For blindedRoleCode, the roles identified map to StudySubject, StudyInvestigator, Assessor, and AssociatedBiologicEntity.
dataMonitoringCommitteeIndicator Qualifier
bridg:InterventionalStudyProtocolVersion
If dataMonitoringCommitteeIndicator = "false", there must not be an associated OversightCommittee (via StudyOversightAuthority) with typeCode = "data monitoring committee".
bridg:InterventionalStudyProtocolVersion
urn:C3PR:Study.type
bridg:InterventionalStudyProtocolVersion
urn:CTGOV:Study_Type_-_Interventional
bridg:InterventionalStudyProtocolVersion
urn:CTRPv1.0:InterventionalStudyProtocol
bridg:InterventionalStudyProtocolVersion
urn:CTRPv3.8:InterventionalStudyProtocol
bridg:InterventionalStudyProtocolVersion
urn:CTRR:Study_Type
bridg:InterventionalStudyProtocolVersion
urn:CTRRr3:InterventionalStudy
bridg:InterventionalStudyProtocolVersion
urn:CTRRr3:Study.typeCode
bridg:InterventionalStudyProtocolVersion
urn:CTRv1.0:InterventionalStudyProtocolVersion
bridg:InterventionalStudyProtocolVersion
urn:WHO:Study_Type
bridg:Laboratory
Laboratory
bridg:Laboratory
false
bridg:Laboratory
An organization with the capability and competency to perform scientific research, experiments and measurements.
bridg:Laboratory
urn:CTRv1.0:Laboratory
bridg:Laboratory
urn:HL7SP:ServiceProvider
bridg:Manufacturer
Manufacturer
bridg:Manufacturer
false
bridg:Manufacturer
bridg:Manufacturer
urn:CTRv1.0:Manufacturer
in R_Product
bridg:Manufacturer
urn:ICSRr2:performance1
bridg:Material
Material
bridg:Material
false
bridg:Material
A physical substance.
bridg:Material
drug
bridg:Material
device
bridg:Material
specimen
Attribute Set actualIndicator Qualifier
bridg:Material
effectiveDateRange is valid only when actualIndicator = "true".
bridg:Material
urn:CTRPv1.0:Material
bridg:Material
urn:CTRRr3:Material
bridg:Material
urn:CTRv1.0:Material
in R_Specimen universal
bridg:Material
urn:ICSRr2:ManufacturedMaterial
in R_Specimen universal
bridg:Material
urn:ICSRr2:Natural
bridg:MaterialIdentifier
MaterialIdentifier
bridg:MaterialIdentifier
false
bridg:MaterialIdentifier
The unique identification of a material in a specific context.
bridg:MaterialIdentifier
This class is a resolution of the requirement for noting the type of an identifier which is not handled by the purely technical HL7 II data type.
be assigned by actualIndicator Qualifier
bridg:MaterialIdentifier
Only Organization with actualIndicator = "true" is valid.
bridg:MaterialIdentifier
urn:CTRv1.0:MaterialIdentifier
in R_Product
bridg:MaterialIdentifier
urn:ICSRr2:IdentifiedItem
bridg:MaterialName
MaterialName
bridg:MaterialName
false
bridg:MaterialName
The non-unique textual identification of a material in a specified context.
bridg:MaterialName
urn:CTRv1.0:MaterialName
in R_Product
bridg:MaterialName
urn:ICSRr2:NamedEntity
bridg:MaterialResource
MaterialResource
bridg:MaterialResource
false
bridg:MaterialResource
Physical supplies provided by an individual company, institution, or organization for the conduct of research.
bridg:MaterialResource
In kind contributions
bridg:MaterialResource
donations of study drug
bridg:MaterialResource
device
bridg:MaterialResource
etc.
s of Monetary or Material Support
bridg:MaterialResource
urn:CTRR:Source
bridg:NotificationReceiver
NotificationReceiver
bridg:NotificationReceiver
false
bridg:NotificationReceiver
A person or organization that is the target of a notification.
be a function performed by Exclusive Or
bridg:NotificationReceiver
A Notification Receiver might be a function performed by one and only one of the following: HealthcareProvider, ReportSubmitter, DocumentAuthor, Organization, StudyPersonnel, StudySitePersonnel.
bridg:NotificationReceiver
urn:C3PRv2.9:UserBasedRecipient
bridg:NotificationReceiver
urn:C3PRv2.9:Recipient
bridg:NotificationReceiver
urn:caAERSv2.2:ContactMechanismBasedRecipient
bridg:NotificationReceiver
urn:caAERSv2.2:Recipient
bridg:NotificationReceiver
urn:caAERSv2.2:RoleBasedRecipient
bridg:ObservationResultActionTakenRelationship
ObservationResultActionTakenRelationship
bridg:ObservationResultActionTakenRelationship
false
bridg:ObservationResultActionTakenRelationship
Specifies the link between an observation result and the actions taken as a result of that relationship
bridg:ObservationResultActionTakenRelationship
An electrical problem (product investigation result) in a device could result in a recall (product action taken) of the device.
bridg:ObservationResultActionTakenRelationship
An abnormal lab result triggers a follow-up lab test for further investingation.
bridg:ObservationResultActionTakenRelationship
Study dose reduced or protocol treatment change due to an adverse event.
bridg:ObservationResultActionTakenRelationship
AdverseEventActionTakenRelationship
bridg:ObservationResultActionTakenRelationship
ProductActionTakenRelationship
bridg:ObservationResultActionTakenRelationship
Action taken relationship is generally used for "unplanned" activities rather than those already determined in "contingent" relationships in the planned study design.
bridg:ObservationResultActionTakenRelationship
urn:AE:ActionTaken
bridg:ObservationResultActionTakenRelationship
urn:AE:ProductInvestigation.productReturnedIndicator
bridg:ObservationResultActionTakenRelationship
urn:AE:ProductInvestigation.remedialActionTaken
bridg:ObservationResultActionTakenRelationship
urn:CTRv1.0:ObservationResultActionTakenRelationship
bridg:ObservationResultActionTakenRelationship
urn:CTRv1.0:AdverseEventActionTakenRelationship
bridg:ObservationResultActionTakenRelationship
urn:CTRv1.0:ProductActionTakenRelationship
bridg:ObservationResultActionTakenRelationship
urn:NCI_CRF_Standard:CDE_2435042v1.2:_Protocol_Deviation_Action_Text
bridg:ObservationalStudyProtocolVersion
ObservationalStudyProtocolVersion
bridg:ObservationalStudyProtocolVersion
false
bridg:ObservationalStudyProtocolVersion
An action plan of a pre-clinical or clinical study in which biomedical and/or health outcomes are assessed in pre-defined groups of study subjects or experimental units. Study subjects or experimental units in the study may receive diagnostic, therapeutic, or other interventions, but the investigator does not assign specific interventions to the study subjects or experimental units of the study.
bridg:ObservationalStudyProtocolVersion
urn:C3PR:Study.type
bridg:ObservationalStudyProtocolVersion
urn:CTGOV:Study_Type_-_Observational
bridg:ObservationalStudyProtocolVersion
urn:CTRR:Study_Type
bridg:ObservationalStudyProtocolVersion
urn:CTRRr3:Study.typeCode
bridg:ObservationalStudyProtocolVersion
urn:CTRRr3:ObservationalStudy
bridg:ObservationalStudyProtocolVersion
urn:CTRv1.0:ObservationalStudyProtocolVersion
bridg:ObservationalStudyProtocolVersion
urn:WHO:Study_Type
bridg:Organization
Organization
bridg:Organization
false
bridg:Organization
A formalized group of persons or other organizations collected together for a common purpose (such as administrative, legal, political) and the infrastructure to carry out that purpose.
bridg:Organization
US National Cancer Institute (NCI); CDISC; HL7
bridg:Organization
ACME Corporation
Attribute Set actualIndicator Qualifier
bridg:Organization
name, postalAddress, telecomAddress are valid only when actualIndicator = "true".
bridg:Organization
urn:C3PRv2.9:HealthcareSite
bridg:Organization
urn:C3PRv2.9:Organization
bridg:Organization
urn:CTRPv1.0:Organization
bridg:Organization
urn:CTRPv3.8:OrganizationalGroup
bridg:Organization
urn:CTRPv3.8:Organization
bridg:Organization
urn:CTRR:Protocol_Identifier_Source
bridg:Organization
urn:CTRRr3:Organization
bridg:Organization
urn:CTRv1.0:Organization
bridg:Organization
urn:HL7SP:Organization
bridg:Organization
urn:HL7SP:LicenseIssuer
in E_Organization informational
bridg:Organization
urn:ICSRr2:Organization
in R_Product
bridg:Organization
urn:ICSRr2:ProductIdentifierIssuer
in R_Product
bridg:Organization
urn:ICSRr2:Organization
in IndividualCaseSafetyReport
bridg:Organization
urn:ICSRr2:TerritorialAuthority
in R_Product
bridg:Organization
urn:ICSRr2:Agency
in IndividualCaseSafetyReport
bridg:Organization
urn:ICSRr2:Organization
bridg:Organization
urn:LabViewer2.2:Organization
bridg:OrganizationIdentifier
OrganizationIdentifier
bridg:OrganizationIdentifier
false
bridg:OrganizationIdentifier
The unique identification of an organization in a specified context.
bridg:OrganizationIdentifier
This class is a resolution of the requirement for noting the type of an identifier which is not handled by the purely technical HL7 II data type.
be assigned by Exclusive Or
bridg:OrganizationIdentifier
An OrganizationIdentifier is assigned by one and only one of the following: Organization, SystemOfRecord.
be assigned by actualIndicator Qualifier
bridg:OrganizationIdentifier
Only Organization with actualIndicator = "true" is valid.
identifies actualIndicator Qualifier
bridg:OrganizationIdentifier
Only Organization with actualIndicator = "true" is valid.
bridg:OrganizationIdentifier
urn:CTRPv3.8:IdentifiedEntity
bridg:OrganizationIdentifier
urn:CTRv1.0:OrganizationIdentifier
in IndividualCaseSafetyReport
bridg:OrganizationIdentifier
urn:ICSRr2:IdentifiedEntity2
bridg:OrganizationIdentifier
urn:caAERSv2.2:OrganizationAssignedIdentifier
bridg:OrganizationRelationship
OrganizationRelationship
bridg:OrganizationRelationship
false
bridg:OrganizationRelationship
Specifies the link between one organization and another.
bridg:OrganizationRelationship
The relationship between an organization and its legal representative
bridg:OrganizationRelationship
the whole/part relationship between an organization and its sub organizations (e.g. departments
bridg:OrganizationRelationship
divisions).
bridg:OrganizationRelationship
urn:CTRPv3.8:OrganizationalGroupRelationship
bridg:OrganizationRelationship
urn:CTRPv3.8:OrganizationalRelationship
bridg:OrganizationRelationship
urn:CTRRr3:OrganizationRelationship
bridg:OrganizationRelationship
urn:CTRv1.0:OrganizationRelationship
Universal
bridg:OrganizationRelationship
urn:HL7SD:E_Organization
in R_Product
bridg:OrganizationRelationship
urn:ICSRr2:AssignedEntity
in R_Product
bridg:OrganizationRelationship
urn:ICSRr2:AssignedEntity3
in IndividualCaseSafetyReport
bridg:OrganizationRelationship
urn:ICSRr2:AssignedEntity2
bridg:OrganizationalContact
OrganizationalContact
bridg:OrganizationalContact
false
bridg:OrganizationalContact
A person who provides or receives information on behalf of an organization.
be a function performed by actualIndicator Qualifier
bridg:OrganizationalContact
Only Person with actualIndicator = "true" is valid.
handles communication for actualIndicator Qualifier
bridg:OrganizationalContact
Only Organization with actualIndicator = "true" is valid.
bridg:OrganizationalContact
urn:AE:ContactPerson
bridg:OrganizationalContact
urn:CTRPv1.0:OrganizationalContact
bridg:OrganizationalContact
urn:CTRPv3.8:OrganizationalContact
bridg:OrganizationalContact
urn:CTRRr3:OrganizationalContact
bridg:OrganizationalContact
urn:CTRv1.0:OrganizationalContact
in E_Organization informational
bridg:OrganizationalContact
urn:ICSRr2:ContactParty
in R_Product
bridg:OrganizationalContact
urn:ICSRr2:contactParty
in IndividualCaseSafetyReport
bridg:OrganizationalContact
urn:ICSRr2:ContactParty
bridg:OversightAuthority
OversightAuthority
bridg:OversightAuthority
false
bridg:OversightAuthority
An organization with monitoring, regulatory, or supervisory authority over biomedical research at the local, regional, national, or international level.
bridg:OversightAuthority
Medicines and Healthcare Products Regulatory Agency (MHRA) in the UK
bridg:OversightAuthority
Food and Drug Administration (FDA) in the USA
bridg:OversightAuthority
World Health Organization (WHO)
bridg:OversightAuthority
Institutional Review Board (IRB)
bridg:OversightAuthority
Ethics committee
bridg:OversightAuthority
Research ethics board
bridg:OversightAuthority
urn:CTRR:Oversight_Authority
bridg:OversightAuthority
urn:CTRRr3:OversightAuthority
bridg:OversightAuthority
urn:CTRv1.0:OversightAuthority
bridg:OversightCommittee
OversightCommittee
bridg:OversightCommittee
false
bridg:OversightCommittee
An organization that approves, monitors and reviews biomedical research to protect the rights, safety and welfare of the study subjects. This committee performs critical oversight functions for research conducted on human study subjects that are scientific, ethical, and regulatory.
bridg:OversightCommittee
Institutional Review Board (IRB)
bridg:OversightCommittee
ethics committee
bridg:OversightCommittee
research ethics board
bridg:OversightCommittee
urn:CTOM:HealthcareSiteParticipantRole.roleCode
bridg:OversightCommittee
urn:CTRPv1.0:OversightCommittee
bridg:OversightCommittee
urn:CTRPv3.8:OversightCommittee
bridg:OversightCommittee
urn:CTRRr3:OversightCommittee
bridg:OversightCommittee
urn:CTRv1.0:OversightCommittee
bridg:OversightCommittee
urn:HL7SP:ServiceProvider
bridg:OversightCommittee
urn:HL7SP:Verifier
bridg:OversightCommittee
urn:HL7SP:EthicalCommittee
bridg:OversightCommittee
urn:HSDBv1.0:[Lead_Organization]_.Organization_Type
bridg:Package
Package
bridg:Package
false
bridg:Package
A container within which the product is delivered or shipped.
bridg:Package
a shipping carton
bridg:Package
bottle
bridg:Package
urn:AE:Package
bridg:Package
urn:CTRv1.0:Package
in R_Product
bridg:Package
urn:ICSRr2:PackagedProduct
bridg:PerformedActivity
PerformedActivity
bridg:PerformedActivity
false
bridg:PerformedActivity
An activity that is successfully or unsuccessfully completed.
bridg:PerformedActivity
CBC performed on a specific StudySubject on a given day.
bridg:PerformedActivity
A scheduled blood draw that is missed by a specific ExperimentalUnit on a given day.
be participated in by actualIndicator Qualifier
bridg:PerformedActivity
Only BiologicEntity, BiologicEntityGroup, Material, ProductGroup or Organization (via Subject or ExperimentalUnit) with actualIndicator = “true” is valid.
be performed by actualIndicator Qualifier
bridg:PerformedActivity
Only Person, Organization or Device (via Performer) with actualIndicator = "true" is valid.
containingEpoch Qualifier
bridg:PerformedActivity
The containing Epoch association must not be present for PerformedActivities that instantiate PlannedActivities (or ScheduledActivites that instantiate PlannedActivities) with an association to Epoch.
dateRange Qualifier
bridg:PerformedActivity
When PerformedObservation.focalDateRange is present, PerformedObservation.dateRange must be a single date.
instantiates Exclusive Or
bridg:PerformedActivity
A PerformedActivity must instantiate one and only one of the following: DefinedActivity, PlannedActivity, ScheduledActivity.
occurs in the context of Qualifier
bridg:PerformedActivity
A PerformedActivity is only directly related to a StudyProtocolVersion if it is instantiating a PlannedActivity or ScheduledActivity (not a DefinedActivity).
bridg:PerformedActivity
urn:AE:PerformedActivity
bridg:PerformedActivity
urn:C3PRv2.9:ScheduledArm
bridg:PerformedActivity
urn:CTRPv3.8:PerformedActivity
bridg:PerformedActivity
urn:CTRv1.0:PerformedActivity
in R_Product
bridg:PerformedActivity
urn:ICSRr2:productActChoice
in R_Product
bridg:PerformedActivity
urn:ICSRr2:ProductEvent
bridg:PerformedActivity
urn:LabViewer2.2:Activity
bridg:PerformedActivity
urn:PSCv2.6:Occurred
bridg:PerformedActivity
urn:SDTM_IGv3.1.2:SE.DOMAIN
bridg:PerformedActivity
urn:SDTM_IGv3.1.2:SV.DOMAIN
bridg:PerformedActivity
urn:caAERSv2.2:AdverseEventReportingPeriod
bridg:PerformedActivity
urn:caAERSv2.2:TreatmentInformation
bridg:PerformedActivity
urn:caAERSv2.2:CourseDate
bridg:PerformedAdministrativeActivity
PerformedAdministrativeActivity
bridg:PerformedAdministrativeActivity
false
bridg:PerformedAdministrativeActivity
The completed action within the context of a given study that is not directly related to the study's overarching hypothesis evaluation or testing, but is nonetheless essential to the efficient and/or effective coordination and execution of the study.
bridg:PerformedAdministrativeActivity
assignment to a treatment arm
bridg:PerformedAdministrativeActivity
registration to a study
bridg:PerformedAdministrativeActivity
start of on-study period
bridg:PerformedAdministrativeActivity
end of on-study period
bridg:PerformedAdministrativeActivity
obtain informed consent
bridg:PerformedAdministrativeActivity
verify eligibility criteria
bridg:PerformedAdministrativeActivity
enroll
bridg:PerformedAdministrativeActivity
randomize
bridg:PerformedAdministrativeActivity
complete study visits
bridg:PerformedAdministrativeActivity
exit study
bridg:PerformedAdministrativeActivity
break treatment blind
bridg:PerformedAdministrativeActivity
protocol violation
bridg:PerformedAdministrativeActivity
premature withdrawal
bridg:PerformedAdministrativeActivity
etc.
be performed at actualIndicator Qualifier
bridg:PerformedAdministrativeActivity
Only Organization (via StudySite) with actualIndicator = "true" is valid.
bridg:PerformedAdministrativeActivity
urn:CTRPv3.8:PerformedAdministrativeActivity
bridg:PerformedAdministrativeActivity
urn:CTRv1.0:PerformedAdministrativeActivity
bridg:PerformedAdministrativeActivity
urn:HL7SP:RegistrationEvent
bridg:PerformedClinicalInterpretation
PerformedClinicalInterpretation
bridg:PerformedClinicalInterpretation
false
bridg:PerformedClinicalInterpretation
An assessment which involves determining the meaning of one or more other observation results.
bridg:PerformedClinicalInterpretation
The results of a white blood cell count may be interpreted as constituting a grade 2 toxicity.
Derived Attribute Exclusive Or
bridg:PerformedClinicalInterpretation
Only one of the following attributes will be populated in any given instance: toxicityGradeCode, severityCode, clinicallySignificantIndicator, abnormalIndicator.
bridg:PerformedClinicalInterpretation
urn:CTRv1.0:PerformedClinicalInterpretation
bridg:PerformedClinicalInterpretation
urn:HCTv1.0:CDE_2871889:Disease__Disorder_or_Finding.Was_there_a_history_of_clinically_significant_fungal_infection?
bridg:PerformedClinicalResult
PerformedClinicalResult
bridg:PerformedClinicalResult
false
bridg:PerformedClinicalResult
A result of a clinical observation, i.e. from an examination, test or direct observation performed on the experimental unit.
bridg:PerformedClinicalResult
The performed observation of "WBC count" would be associated to a clinical result called "WBC result" in which the results of the observation (7500 WBCs) would be stored.
bridg:PerformedClinicalResult
There is an association between the observation that has the original data (and the original units) and the observation in which the data elements have been converted into standardized units.
If further use case are discovered it may be necessary to move the recursive relationship up to PerformedObservationResult.
reference Qualifier
bridg:PerformedClinicalResult
If a PerformedClinicalResult references a ReferenceResult, it is required that PerformedClinicalResult.typeCode = ReferenceResult.valueTypeCode. It is further required that the fastingStatusIndicator on the PerformedSpecimenCollection that produced the specimen upon which the clinical test was performed = ReferenceResult.fastingStatusIndicator if specified.
bridg:PerformedClinicalResult
urn:CTRv1.0:PerformedClinicalResult
bridg:PerformedClinicalResult
urn:LabViewer2.2:LaboratoryResult
bridg:PerformedClinicalResult
urn:caAERSv2.2:LabValue
bridg:PerformedCompositionRelationship
PerformedCompositionRelationship
bridg:PerformedCompositionRelationship
false
bridg:PerformedCompositionRelationship
A relationship between a composite activity and a component activity that comprises it, i.e. parent and child activities where all activities have occurred in the context of a particular study.
bridg:PerformedCompositionRelationship
An unplanned substance administration occurs as part of a planned encounter.
bridg:PerformedCompositionRelationship
A planned substance administration occurs as part of an encounter that is different than the one in which it was originally planned.
bridg:PerformedCompositionRelationship
An unplanned encounter contains a number of activities.
bridg:PerformedCompositionRelationship
Particularly relevant when one or both of the activities are not planned as the composition relationship can't be established using the normal PlannedCompositionRelationship or DefinedCompositionRelationship.
Composition Relationship Qualifier
bridg:PerformedCompositionRelationship
The PerformedCompositionRelationship class may only be used when there is no DefinedCompositionRelationship or PlannedCompositionRelationship between the objects that the source and target relationship instantiate (directly or indirectly). I.e., if the composition relationship can reasonably be expressed in the defined or planned representation, it must be expressed there, not in the performed representation.
PerformedActivity
bridg:PerformedCompositionRelationship
urn:CTRv1.0:PerformedActivity.contained
bridg:PerformedDiagnosis
PerformedDiagnosis
bridg:PerformedDiagnosis
false
bridg:PerformedDiagnosis
The identification of a disease or illness by examining the signs and symptoms.
bridg:PerformedDiagnosis
urn:C3PRv2.9:DiseaseHistory
bridg:PerformedDiagnosis
urn:CTRv1.0:PerformedDiagnosis
bridg:PerformedDiagnosis
urn:HCTv1.0:CDE_2962088:Involvement_and_Extent_of_Disease.Specify_other_co-existing_phakomatosis:
bridg:PerformedDiagnosis
urn:caAERSv2.2:DiseaseHistory
bridg:PerformedDiagnosis
urn:caAERSv2.2:StudyParticipantDiseaseHistory
bridg:PerformedDiagnosisProcedureRelationship
PerformedDiagnosisProcedureRelationship
bridg:PerformedDiagnosisProcedureRelationship
false
bridg:PerformedDiagnosisProcedureRelationship
Specifies the link between a diagnosis and the procedure performed to address it.
bridg:PerformedEligibilityCriterion
PerformedEligibilityCriterion
bridg:PerformedEligibilityCriterion
false
bridg:PerformedEligibilityCriterion
One of a set of conditions that a study subject must meet in order to participate in a study.
be participated in by Qualifier
bridg:PerformedEligibilityCriterion
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:PerformedEligibilityCriterion
urn:CTRv1.0:PerformedEligibilityCriterion
bridg:PerformedEligibilityCriterion
urn:SDTM_IGv3.1.2:IE.DOMAIN
bridg:PerformedExclusionCriterion
PerformedExclusionCriterion
bridg:PerformedExclusionCriterion
false
bridg:PerformedExclusionCriterion
A characteristic or requirement that disqualifies a subject from participation in a study.
bridg:PerformedExclusionCriterion
pregnancy
bridg:PerformedExclusionCriterion
urn:C3PR:ExclusionEligibilityCriterion
bridg:PerformedExclusionCriterion
urn:CTRv1.0:PerformedExclusionCriterion
bridg:PerformedExperimentalUnitAllocation
PerformedExperimentalUnitAllocation
bridg:PerformedExperimentalUnitAllocation
false
bridg:PerformedExperimentalUnitAllocation
The completed action that is the assignment of an experimental unit to a portion of the study, such as an arm or a portion of an arm (when secondary allocations may occur).
bridg:PerformedExperimentalUnitAllocation
Mrs. Smith is assigned to Arm A.
be participated in by Qualifier
bridg:PerformedExperimentalUnitAllocation
Associations from ExperimentalUnit are valid. Associations from Subject (including StudySubject) are not valid.
bridg:PerformedExperimentalUnitAllocation
urn:NCI_CRF_Standard:CDE_2454528v1.0:_Protocol_Arm_Assignment_Text
bridg:PerformedHistopathology
PerformedHistopathology
bridg:PerformedHistopathology
false
bridg:PerformedHistopathology
The findings from a microscopic study of characteristic tissue abnormalities by employing various cytochemical and immunocytochemical stains.
bridg:PerformedHistopathology
urn:CTRv1.0:PerformedHistopathology
bridg:PerformedImaging
PerformedImaging
bridg:PerformedImaging
false
bridg:PerformedImaging
The completed action of obtaining pictures of the interior or exterior of the body usually for diagnostic reasons.
bridg:PerformedImaging
X-ray
bridg:PerformedImaging
MRI
bridg:PerformedImaging
etc
be participated in by Qualifier
bridg:PerformedImaging
Associations from Subject (including StudySubject) and Experimental Unit are valid for BiologicEntity, BiologicEntityGroup, BiologicEntityPart and Specimen, not for Product, ProductGroup, Organization or HealthcareFacility.
bridg:PerformedImaging
urn:CTRv1.0:PerformedImaging
bridg:PerformedInclusionCriterion
PerformedInclusionCriterion
bridg:PerformedInclusionCriterion
false
bridg:PerformedInclusionCriterion
A characteristic or requirement that a subject must meet to participate in a study.
bridg:PerformedInclusionCriterion
Must be over the age of 18
bridg:PerformedInclusionCriterion
urn:C3PR:InclusionEligibilityCriterion
bridg:PerformedInclusionCriterion
urn:CTRv1.0:PerformedInclusionCriterion
bridg:PerformedLesionDescription
PerformedLesionDescription
bridg:PerformedLesionDescription
false
bridg:PerformedLesionDescription
A characterization of the extent of any localized or abnormal change in the structure of part of an organ or tissue.
bridg:PerformedLesionDescription
urn:CTRv1.0:PerformedLesionDescription
bridg:PerformedMaterialProcessStep
PerformedMaterialProcessStep
bridg:PerformedMaterialProcessStep
false
bridg:PerformedMaterialProcessStep
The completed act of processing a material.
bridg:PerformedMaterialProcessStep
freezing
bridg:PerformedMaterialProcessStep
thawing
bridg:PerformedMaterialProcessStep
spinning
bridg:PerformedMaterialProcessStep
embedding
bridg:PerformedMaterialProcessStep
dividing
bridg:PerformedMaterialProcessStep
aliquot
bridg:PerformedMaterialProcessStep
adding additives or growth factors
bridg:PerformedMaterialProcessStep
product manipulation
bridg:PerformedMaterialProcessStep
Material process may be performed on any kind of material, such as a specimen, nanomaterial, or biologic. The result of the process may a similar or different kind of material, for instance a specimen may be the result of a specimen processing step (e.g., aliquot or division of a specimen), or alternatively a blood product has anticoagulants added to it to preserve the product. Other processsing steps, such as adding growth factor to induce cell growth, may be performed on the blood product.
be participated in by Qualifier
bridg:PerformedMaterialProcessStep
Associations from Subject (including StudySubject) and ExperimentalUnit are valid for Specimen, Product and ProductGroup, not for BiologicEntity, BiologicEntityPart, BiologicEntityGroup, HealthcareFacility or Organization.
bridg:PerformedMaterialStorage
PerformedMaterialStorage
bridg:PerformedMaterialStorage
false
bridg:PerformedMaterialStorage
The completed action of safekeeping harvested material in a depository.
bridg:PerformedMaterialStorage
refrigeration
bridg:PerformedMaterialStorage
cryopreservation
bridg:PerformedMaterialStorage
dehydration
bridg:PerformedMaterialStorage
etc.
bridg:PerformedMaterialStorage
There is a difference between the act of changing the state of material, which is represented by PerformedMaterialProcessStep, and the act of maintaining state of the material by storing it, which is represented by PerformedMaterialStorage.
be participated in by Qualifier
bridg:PerformedMaterialStorage
Associations from Subject (including StudySubject) and ExperimentalUnit are valid for Specimen and Product, not for BiologicEntity, BIologicEntityPart, BiologicEntityGroup, ProductGroup, HealthcareFacility or Organization.
bridg:PerformedMedicalConditionResult
PerformedMedicalConditionResult
bridg:PerformedMedicalConditionResult
false
bridg:PerformedMedicalConditionResult
Any sign, symptom, disease, or other medical occurrence.
bridg:PerformedMedicalConditionResult
death
bridg:PerformedMedicalConditionResult
back pain
bridg:PerformedMedicalConditionResult
headache
bridg:PerformedMedicalConditionResult
pulmonary embolism
bridg:PerformedMedicalConditionResult
heart attack
bridg:PerformedMedicalConditionResult
pregnancy
bridg:PerformedMedicalConditionResult
flu
bridg:PerformedMedicalConditionResult
broken bone
bridg:PerformedMedicalConditionResult
menstrual period
bridg:PerformedMedicalConditionResult
depression
bridg:PerformedMedicalConditionResult
Clinical Events
bridg:PerformedMedicalConditionResult
Medical History
bridg:PerformedMedicalConditionResult
This condition may have been recalled by the subject or a caregiver or provided in their medical record.
bridg:PerformedMedicalConditionResult
urn:CTRv1.0:PerformedMedicalConditionResult
bridg:PerformedMedicalConditionResult
urn:NCI_CRF_Standard:MedicalHistory
bridg:PerformedMedicalConditionResult
urn:caAERSv2.2:StudyParticipantPreExistingCondition
bridg:PerformedNotification
PerformedNotification
bridg:PerformedNotification
false
bridg:PerformedNotification
The completed action within the context of a given study that represents the communication of a message to a recipient.
be participated in by Qualifier
bridg:PerformedNotification
Associations from Subject (including StudySubject) are valid. Associations from ExperimentalUnit are not valid.
be received by actualIndicator Qualifier
bridg:PerformedNotification
Only Person or Organization (via NotificationReceiver) with actualIndicator = "true" is valid.
bridg:PerformedNotification
urn:C3PRv2.9:ScheduledNotification
bridg:PerformedObservation
PerformedObservation
bridg:PerformedObservation
false
bridg:PerformedObservation
The completed action of observing, monitoring, measuring or otherwise qualitatively or quantitatively gathering data or information about one or more aspects of a subject, study subject, or experimental unit.
bridg:PerformedObservation
lab test
bridg:PerformedObservation
taking vital signs
bridg:PerformedObservation
physical exam
be performed by (lab) actualIndicator Qualifier
bridg:PerformedObservation
Only Organization (via PerformingLaboratory) with actualIndicator = "true" is valid.
be reported by Qualifier
bridg:PerformedObservation
A PerformedObservation is reported by an Assessor. The inherited association of Performer (from Activity) is not valid for a PerformedObservation.
be reported by actualIndicator Qualifier
bridg:PerformedObservation
Only Person, Device or Organization (via Assessor) with actualIndicator = "true" is valid.
bridg:PerformedObservation
urn:CTRPv3.8:PerformedObservation
bridg:PerformedObservation
urn:CTRv1.0:PerformedStudyObservation
bridg:PerformedObservation
urn:CTRv1.0:PerformedObservation
in IndividualCaseSafetyReport
bridg:PerformedObservation
urn:ICSRr2:RelatedInvestigation
in IndividualCaseSafetyReport
bridg:PerformedObservation
urn:ICSRr2:Subject7
in IndividualCaseSafetyReport
bridg:PerformedObservation
urn:ICSRr2:InvestigativeEvent
in IndividualCaseSafetyReport
bridg:PerformedObservation
urn:ICSRr2:ObservationEvent
bridg:PerformedObservation
urn:LabViewer2.2:LaboratoryTest
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:EG.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:VS.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:PE.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:MH.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:SC.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:LB.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:MS.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:PC.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:PP.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:FA.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:CE.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:MB.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:QS.DOMAIN
bridg:PerformedObservation
urn:SDTM_IGv3.1.2:CO.DOMAIN
bridg:PerformedObservation
urn:caAERSv2.2:Lab
bridg:PerformedObservationResult
PerformedObservationResult
bridg:PerformedObservationResult
false
bridg:PerformedObservationResult
The finding obtained by observing, monitoring, measuring or otherwise qualitatively or quantitatively recording one or more aspects of physiologic or psychologic processes.
bridg:PerformedObservationResult
urn:C3PRv2.9:SubjectEligibilityAnswer
bridg:PerformedObservationResult
urn:CTRPv3.8:ObservationResult
bridg:PerformedObservationResult
urn:CTRPv3.8:PerformedObservationResult
bridg:PerformedObservationResult
urn:CTRv1.0:PerformedObservationResult
bridg:PerformedObservationResult
urn:HCTv1.0:CDE_2769634:Adverse_Events.Specify_other_most_likely_cause_of_the_adverse_event:
in IndividualCaseSafetyReport
bridg:PerformedObservationResult
urn:ICSRr2:InvestigationCharacteristic
in R_Product
bridg:PerformedObservationResult
urn:ICSRr2:Characteristics
bridg:PerformedProcedure
PerformedProcedure
bridg:PerformedProcedure
false
bridg:PerformedProcedure
The completed action whose immediate and primary intention is the alteration of the physical or mental condition of the subject, study subject or experimental unit.
bridg:PerformedProcedure
Procedures may involve the disruption of some body surface (e.g. an incision in a surgical procedure) conservative procedures such as reduction of a luxated joint
bridg:PerformedProcedure
including physiotherapy such as chiropractic treatment
bridg:PerformedProcedure
massage
bridg:PerformedProcedure
balneotherapy
bridg:PerformedProcedure
acupuncture
bridg:PerformedProcedure
shiatsu
bridg:PerformedProcedure
counseling
bridg:PerformedProcedure
etc.
uses actualIndicator Qualifier
bridg:PerformedProcedure
Only Product with actualIndicator = "true" is valid.
bridg:PerformedProcedure
urn:AE:Intervention
bridg:PerformedProcedure
urn:CTRv1.0:PerformedProcedure
in IndividualCaseSafetyReport
bridg:PerformedProcedure
urn:ICSRr2:ProductUseReference
in A_ProductReportingRelevantInformation
bridg:PerformedProcedure
urn:ICSRr2:Procedure
bridg:PerformedProcedure
urn:caAERSv2.2:TreatmentAssignment
bridg:PerformedProcedure
urn:caAERSv2.2:SurgeryIntervention
bridg:PerformedProcedure
urn:caAERSv2.2:RadiationIntervention
bridg:PerformedProcedure
urn:caAERSv2.2:StudyParticipantPriorTherapy
bridg:PerformedProductInvestigation
PerformedProductInvestigation
bridg:PerformedProductInvestigation
false
bridg:PerformedProductInvestigation
The completed process of evaluating a product after it has been returned to the manufacturer or reprocessor.
be participated in by Qualifier
bridg:PerformedProductInvestigation
Associations from Subject (including StudySubject) are valid only for Product, not for BiologicEntity, BiologicEntityGroup, Specimen, HealthcareFacility or Organization. Associations from ExperimentalUnit are not valid.
is triggered by Exclusive Or
bridg:PerformedProductInvestigation
A PerformedProductInvestigation is triggered by one and only one of the following: AdverseEvent, PerformedProductProblemDiscovery.
bridg:PerformedProductInvestigation
urn:AE:ProductInvestigation
bridg:PerformedProductInvestigation
urn:CTRv1.0:PerformedProductInvestigation
in IndividualCaseSafetyReport
bridg:PerformedProductInvestigation
urn:ICSRr2:Subject5
in IndividualCaseSafetyReport
bridg:PerformedProductInvestigation
urn:ICSRr2:Subject6
in IndividualCaseSafetyReport
bridg:PerformedProductInvestigation
urn:ICSRr2:ProductDefectAssessment
bridg:PerformedProductInvestigationResult
PerformedProductInvestigationResult
bridg:PerformedProductInvestigationResult
false
bridg:PerformedProductInvestigationResult
Information captured while conducting research on a product.
bridg:PerformedProductInvestigationResult
An electrical problem in a device.
bridg:PerformedProductInvestigationResult
urn:CTRv1.0:PerformedProductInvestigationResult
bridg:PerformedProductProblemDiscovery
PerformedProductProblemDiscovery
bridg:PerformedProductProblemDiscovery
false
bridg:PerformedProductProblemDiscovery
The recognition of a product defect that needs to be reported.
bridg:PerformedProductProblemDiscovery
An imaging device is discovered to be leaking radiation. This was discovered on Jan. 10th
bridg:PerformedProductProblemDiscovery
but it suspected to have been leaking for a week. This element maps to the ProductDefectDiscovery class in ICSR and maps to the MedWatch Form 3500A section B1 (Product problem checkbox).
bridg:PerformedProductProblemDiscovery
The BRIDG SCC has a GForge Tracker Issue (#31893) indicating a need to validate the requirement that every PerformedProductProblemDiscovery be described by a SafetyReportVersion.
bridg:PerformedProductProblemDiscovery
urn:AE:ProductProblemDiscovery
bridg:PerformedProductProblemDiscovery
urn:CTRv1.0:PerformedProductProblemDiscovery
in IndividualCaseSafetyReport
bridg:PerformedProductProblemDiscovery
urn:ICSRr2:DefectReference
bridg:PerformedProductTransport
PerformedProductTransport
bridg:PerformedProductTransport
false
bridg:PerformedProductTransport
A completed action of transporting a product between a point of origin and a point of destination.
bridg:PerformedProductTransport
Delivery of drugs from the manufacturer to a medical facility.
ServiceDeliveryLocation Qualifier
bridg:PerformedProductTransport
At least the origin or destination ServiceDeliveryLocation must be known for a PerformedProductTransport.
be participated in by Qualifier
bridg:PerformedProductTransport
Associations from Subject (including StudySubject) are valid for Product, not for BiologicEntity, BiologicEntityGroup, Specimen, HealthcareFacility or Organization. Associations from ExperimentalUnit are not valid.
have destination actualIndicator Qualifier
bridg:PerformedProductTransport
Only Organization (via ServiceDeliveryLocation) with actualIndicator = "true" is valid.
originates at actualIndicator Qualifier
bridg:PerformedProductTransport
Only Organization (via ServiceDeliveryLocation) with actualIndicator = "true" is valid.
bridg:PerformedProductTransport
urn:CTRv1.0:PerformedProductTransport
in R_Product
bridg:PerformedProductTransport
urn:ICSRr2:TransportationEvent
in R_Product
bridg:PerformedProductTransport
urn:ICSRr2:Destination
in R_Product
bridg:PerformedProductTransport
urn:ICSRr2:Origin
bridg:PerformedProtocolDeviation
PerformedProtocolDeviation
bridg:PerformedProtocolDeviation
false
bridg:PerformedProtocolDeviation
A designation of an event as a variation from process or procedures defined in a study protocol.
bridg:PerformedProtocolDeviation
Study subject not withdrawn as per protocol
bridg:PerformedProtocolDeviation
excluded concomitant medication
bridg:PerformedProtocolDeviation
treatment deviation.
bridg:PerformedProtocolDeviation
Deviations usually do not preclude the overall evaluability of subject data for either efficacy or safety.
be addressed by actualIndicator Qualifier
bridg:PerformedProtocolDeviation
Only Person (via StudySitePersonnel) with actualIndicator = "true" is valid.
be authorized by actualIndicator Qualifier
bridg:PerformedProtocolDeviation
Only Person or Organization (via StudyLegalSponsor) with actualIndicator = "true" is valid.
be managed by actualIndicator Qualifier
bridg:PerformedProtocolDeviation
Only Person (via StudyResearchCoordinator) with actualIndicator = "true" is valid.
bridg:PerformedProtocolDeviation
urn:CTRv1.0:PerformedProtocolDeviation
bridg:PerformedProtocolDeviation
urn:NCI_CRF_Standard:ProtocolDeviation
bridg:PerformedProtocolDeviation
urn:SDTM_IGv3.1.2:DV.DOMAIN
bridg:PerformedSpecimenCollection
PerformedSpecimenCollection
bridg:PerformedSpecimenCollection
false
bridg:PerformedSpecimenCollection
The completed action of gathering samples that may be used for subsequent analysis.
bridg:PerformedSpecimenCollection
blood draw
be performed by (lab) actualIndicator Qualifier
bridg:PerformedSpecimenCollection
Only Organization (via CollectingLaboratory) with actualIndicator = "true" is valid.
results in actualIndicator Qualifier
bridg:PerformedSpecimenCollection
Only Material (via Specimen) with actualIndicator = “true” is valid.
bridg:PerformedSpecimenCollection
urn:CTRv1.0:PerformedSpecimenCollection
in R_Specimen universal
bridg:PerformedSpecimenCollection
urn:ICSRr2:SpecimenCollectionProcess
bridg:PerformedSpecimenCollection
urn:LabViewer2.2:SpecimenCollection
bridg:PerformedStudyAdministrativeActivity
PerformedStudyAdministrativeActivity
bridg:PerformedStudyAdministrativeActivity
false
bridg:PerformedStudyAdministrativeActivity
The completed study level administrative activity that is independent of a study subject.
bridg:PerformedStudyAdministrativeActivity
IRB Approval
bridg:PerformedStudyAdministrativeActivity
site enrollment
bridg:PerformedStudyAdministrativeActivity
FDA audit
be participated in by Not Applicable
bridg:PerformedStudyAdministrativeActivity
Associations from Subject (including StudySubject) and ExperimentalUnit are not valid.
bridg:PerformedStudyAdministrativeActivity
urn:CTRv1.0:PerformedStudyAdministrativeActivity
bridg:PerformedStudyAdministrativeActivity
urn:HL7SP:Study.evaluation
bridg:PerformedStudyAgentTransfer
PerformedStudyAgentTransfer
bridg:PerformedStudyAgentTransfer
false
bridg:PerformedStudyAgentTransfer
The completed action in which an authorized party at a designated study site dispenses or receives a study agent to/from a study subject.
bridg:PerformedStudyAgentTransfer
StudySubject receives a bottle of pills.
bridg:PerformedStudyAgentTransfer
Original units can be derived from the translation attribute of the PQ data type on PerformedStudyAgentTransfer.quantity.
The term "study agent" only pertains within the context of a given study. To make this explicit in BRIDG it was determined that the StudyAgent class would only be used to connect Product to StudyProtocolVersion. All activity-related classes would be associated directly to Product to avoid the issues of activities that may cross study boundaries. To determine if a given activity uses a study agent one need only compare the product used in the activity with the list of products associated to StudyAgent for a given StudyProtocolVersion. It should be noted that this determination could be different for different studies and could evolve over the course of a given study.
be authorized by actualIndicator Qualifier
bridg:PerformedStudyAgentTransfer
Only Person (via StudySiteResearchCoordinator) with actualIndicator = "true" is valid.
be participated in by Qualifier
bridg:PerformedStudyAgentTransfer
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
is a transfer of Qualifier
bridg:PerformedStudyAgentTransfer
Associations from Product are valid only for Products that are associated to StudyAgent with the same StudyProtocolVersion as the StudyProtocolVersion associated to the PerformedStudyAgentTransfer.
is a transfer of actualIndicator Qualifier
bridg:PerformedStudyAgentTransfer
Only Product with actualIndicator = "true" is valid.
bridg:PerformedStudyAgentTransfer
urn:CTRv1.0:PerformedStudyAgentTransfer
bridg:PerformedStudyAgentTransfer
urn:SDTM_IGv3.1.2:DA.DOMAIN
bridg:PerformedStudySubjectMilestone
PerformedStudySubjectMilestone
bridg:PerformedStudySubjectMilestone
false
bridg:PerformedStudySubjectMilestone
The completed action which marks a common administrative landmark for a study subject in the course of a study.
bridg:PerformedStudySubjectMilestone
obtain informed consent
bridg:PerformedStudySubjectMilestone
verify eligibility criteria
bridg:PerformedStudySubjectMilestone
enroll
bridg:PerformedStudySubjectMilestone
registration to a study
bridg:PerformedStudySubjectMilestone
randomize
bridg:PerformedStudySubjectMilestone
assignment to a treatment arm
bridg:PerformedStudySubjectMilestone
start of on-study period
bridg:PerformedStudySubjectMilestone
complete study visits
bridg:PerformedStudySubjectMilestone
end of on-study period
bridg:PerformedStudySubjectMilestone
exit study
bridg:PerformedStudySubjectMilestone
break treatment blind
bridg:PerformedStudySubjectMilestone
premature withdrawal
Date Exclusive Or
bridg:PerformedStudySubjectMilestone
Only one of the date attributes will be populated in any given instance.
be participated in by Qualifier
bridg:PerformedStudySubjectMilestone
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:PerformedStudySubjectMilestone
urn:C3PRv2.9:ScheduledEpoch
bridg:PerformedStudySubjectMilestone
urn:CTRPv3.8:PerformedSubjectMilestone
bridg:PerformedStudySubjectMilestone
urn:CTRv1.0:PerformedStudySubjectMilestone
bridg:PerformedStudySubjectMilestone
urn:LabViewer2.2:SubjectAssignment
bridg:PerformedStudySubjectMilestone
urn:NCI_CRF_Standard:Registration
bridg:PerformedStudySubjectMilestone
urn:NCI_CRF_Standard:Enrollment
bridg:PerformedStudySubjectMilestone
urn:SDTM_IGv3.1.2:DS.DOMAIN
bridg:PerformedSubstanceAdministration
PerformedSubstanceAdministration
bridg:PerformedSubstanceAdministration
false
bridg:PerformedSubstanceAdministration
The completed action of applying, introducing or otherwise giving medications or other substances to the subject or experimental unit.
bridg:PerformedSubstanceAdministration
An experimental unit who receives methotrexate as part of chemotherapy
bridg:PerformedSubstanceAdministration
radiation therapy.
bridg:PerformedSubstanceAdministration
For a SubstanceAdministration
bridg:PerformedSubstanceAdministration
targetAnatomicSiteCode = coronary artery
bridg:PerformedSubstanceAdministration
approachAnatomicSiteCode = groin
bridg:PerformedSubstanceAdministration
routeOfAdministrationCode = intra-arterial.
Active Ingredient Qualifier
bridg:PerformedSubstanceAdministration
activeIngredientDose, periodActiveIngredientDoseTotal must only be used when the PerformedSubstanceAdministration is associated to a StudyAgent that has only one active ingredient. Otherwise, it would be ambiguous to which active ingredient the amounts indicated in these attributes apply.
Dose Qualifier
bridg:PerformedSubstanceAdministration
productDose, periodProductDoseTotal, treatmentVehicleAmount, activeIngredientDose, periodActiveIngredientDoseTotal must only be used when the PerformedSubstanceAdministration is associated to a single StudyAgent. Otherwise, it would be ambiguous to which agent the amounts indicated in these attributes apply.
be participated in by Qualifier
bridg:PerformedSubstanceAdministration
Associations from Subject (including StudySubject) are valid only for BiologicEntity, BiologicEntityGroup and Specimen, not for Product, HealthcareFacility or Organization. Associations from ExperimentalUnit are valid for BiologicEntity, BiologicEntityGroup, BiologicEntityPart and Specimen, but not for Product or ProductGroup.
relativeToReference Qualifier
bridg:PerformedSubstanceAdministration
endRelativeToReference must not logically precede the startRelativeToReference. For example, if startRelativeToReference is "during", endRelativeToReference must not be "before".
substanceUnknownIndicator Qualifier
bridg:PerformedSubstanceAdministration
PerformedSubstanceAdministration.substanceUnknownIndicator must = "false" if an association from this procedure to a product exists.
bridg:PerformedSubstanceAdministration
urn:AE:Intervention
bridg:PerformedSubstanceAdministration
urn:CTRv1.0:PerformedSubstanceAdministration
bridg:PerformedSubstanceAdministration
urn:HCTv1.0:CDE_3040303:Therapies.Was_another_radioisotope_administered?
bridg:PerformedSubstanceAdministration
urn:HCTv1.0:CDE_2934704:Therapies.Were_tyrosine_kinase_inhibitors_administered?
bridg:PerformedSubstanceAdministration
urn:SDTM_IGv3.1.2:SU.DOMAIN
bridg:PerformedSubstanceAdministration
urn:SDTM_IGv3.1.2:EX.DOMAIN
bridg:PerformedSubstanceAdministration
urn:SDTM_IGv3.1.2:CM.DOMAIN
bridg:PerformedSubstanceAdministration
urn:caAERSv2.2:StudyParticipantConcomitantMedication
bridg:PerformedSubstanceAdministration
urn:caAERSv2.2:StudyParticipantPriorTherapy
bridg:PerformedSubstanceExtraction
PerformedSubstanceExtraction
bridg:PerformedSubstanceExtraction
false
bridg:PerformedSubstanceExtraction
The completed action of extracting something from an associated study subject for the purpose of the extracted product to be administered to a study subject.
bridg:PerformedSubstanceExtraction
A donor giving Bone Marrow Stem Cells for a Stem Cell Transplant
bridg:PerformedSubstanceExtraction
The study subject could be the same for the extraction and the intended administration.
This is different than a PerformedSpecimenCollection, in that the intent is different: This is a donation.
produces actualIndicator Qualifier
bridg:PerformedSubstanceExtraction
Only Biologic with actualIndicator = "true" is valid.
bridg:Performer
Performer
bridg:Performer
false
bridg:Performer
A person, organization or device that participates in an activity.
bridg:Performer
surgeon
bridg:Performer
performing laboratory
bridg:Performer
monitoring device
be a function performed by Exclusive Or
bridg:Performer
A Performer might be a function performed by one and only one of the following: Person, Organization, Device.
bridg:Performer
urn:AE:PerformingParty
bridg:Performer
urn:CTRRr3:Performer
bridg:Performer
urn:CTRv1.0:Performer
Universal
bridg:Performer
urn:HL7SD:R_AssignedEntity
in R_Product
bridg:Performer
urn:ICSRr2:author
in R_Product
bridg:Performer
urn:ICSRr2:performer
in IndividualCaseSafetyReport
bridg:Performer
urn:ICSRr2:AssignedEntity
in IndividualCaseSafetyReport
bridg:Performer
urn:ICSRr2:participant3
bridg:Performer
urn:TDM:PlannedSubjectActivity.whoPerforms
bridg:Performer
urn:caAERSv2.2:MedicalDevice.otherDeviceOperator
bridg:PerformingLaboratory
PerformingLaboratory
bridg:PerformingLaboratory
false
bridg:PerformingLaboratory
The laboratory that actually performed the test and that is also therefore the source of the data.
bridg:PerformingLaboratory
A laboratory providing analyses of samples collected in clinical care or research.
bridg:PerformingLaboratory
urn:CTRv1.0:PerformingLaboratory
bridg:PerformingLaboratory
urn:LabViewer2.2:PerformingLaboratory
bridg:Person
Person
bridg:Person
false
bridg:Person
A human being.
Attribute Set actualIndicator Qualifier
bridg:Person
name, birthDate, deathDate, initials, postalAddress, telecomAddress are valid only when actualIndicator = "true".
bridg:Person
urn:AE:Person
bridg:Person
urn:C3PRv2.9:Person
bridg:Person
urn:CTRPv1.0:Person
bridg:Person
urn:CTRPv3.8:Person
bridg:Person
urn:CTRRr3:Person
bridg:Person
urn:CTRv1.0:Person
bridg:Person
urn:HL7SD:Person
bridg:Person
urn:HL7SP:Person
bridg:Person
urn:HL7SP:InvestigativePerson
in IndividualCaseSafetyReport
bridg:Person
urn:ICSRr2:Person2
in E_Organization informational
bridg:Person
urn:ICSRr2:ContactPerson
in R_Product
bridg:Person
urn:ICSRr2:AssignedEntity2
in IndividualCaseSafetyReport
bridg:Person
urn:ICSRr2:Person
in R_Product
bridg:Person
urn:ICSRr2:contactPerson
bridg:Person
urn:LabViewer2.2:Person
bridg:Person
urn:NCI_CRF_Standard:Demography
bridg:Person
urn:caAERSv2.2:Person
bridg:Place
Place
bridg:Place
false
bridg:Place
A bounded physical location which may contain structures.
bridg:Place
ambulance
bridg:Place
helicopter
bridg:Place
manufacturing site
bridg:Place
service delivery location
bridg:Place
home
bridg:Place
emergency department
bridg:Place
surgical suite
bridg:Place
patient room
bridg:Place
Constraints: Place may be natural or man-made. The geographic position of a place may or may not be constant.
Discussion: Places may be work facilities (where relevant acts occur), homes (where people live) or offices (where people work). Places may contain sub-places (floor, room, booth, bed). Places may also be sites that are investigated in the context of health care, social work, public health administration (e.g., buildings, picnic grounds, day care centers, prisons, counties, states, and other focuses of epidemiological events).
physicalAddress Qualifier
bridg:Place
physicalAddress should not contain PO Box address parts.
bridg:Place
urn:AE:ServiceDeliveryLocation
bridg:Place
urn:CTRv1.0:Place
in A_ProductReportingRelevantInformation
bridg:Place
urn:ICSRr2:LocatedEntity
in IndividualCaseSafetyReport
bridg:Place
urn:ICSRr2:Place
in A_ProductReportingRelevantInformation
bridg:Place
urn:ICSRr2:Location
in E_Place universal
bridg:Place
urn:ICSRr2:Place
in R_Product
bridg:Place
urn:ICSRr2:territory
bridg:PlannedActivity
PlannedActivity
bridg:PlannedActivity
false
bridg:PlannedActivity
An activity that is intended to occur or start at some point in the context of a particular study.
bridg:PlannedActivity
Pregnancy tests are planned for study subjects who are females of childbearing potential.
bridg:PlannedActivity
A PlannedActivity may be a container of other activities and have a complex structure involving components, options and contingencies using the associated relationship classes. This structure allows the representation of concepts in previous versions of BRIDG such as StudyCells, StudySegments and StudySubjectEncounters. A PlannedActivity could also be thought of as an activity at a particular stage in the business process in which the activities occur, i.e., in the "planned" stage rather than the "scheduled" stage or the "performed" stage. An instance of a PlannedActivity is not assigned to a particular Subject, StudySubject, or ExperimentalUnit, but to a "kind of" Subject, StudySubject, or ExperimentalUnit.
Repeat Duration or Quantity Exclusive Or
bridg:PlannedActivity
A PlannedActivity may have a value for one and only one of the following: repeatDuration or repeatQuantity.
Repeat Frequency Exclusive Or
bridg:PlannedActivity
A PlannedActivity may have a value for one and only one of the following: repeatFrequencyCode or repeatFrequencyRatio.
be participated in by actualIndicator Qualifier
bridg:PlannedActivity
Only BiologicEntity, BiologicEntityGroup, Material, ProductGroup or Organization (via Subject or ExperimentalUnit) with actualIndicator = "false" are valid.
bridg:PlannedActivity
urn:C3PRv2.9:ExclusionEligibilityCriteria
bridg:PlannedActivity
urn:C3PRv2.9:EligibilityCriteria
bridg:PlannedActivity
urn:C3PRv2.9:PhoneCallRandomization
bridg:PlannedActivity
urn:C3PRv2.9:Randomization
bridg:PlannedActivity
urn:C3PRv2.9:Arm
bridg:PlannedActivity
urn:C3PRv2.9:InclusionEligibilityCriteria
bridg:PlannedActivity
urn:CTRPv3.8:Intervention
bridg:PlannedActivity
urn:CTRPv3.8:PlannedActivity
bridg:PlannedActivity
urn:CTRRr3:PlannedActivity
bridg:PlannedActivity
urn:CTRRr3:PlannedIntervention
bridg:PlannedActivity
urn:CTRv1.0:PlannedActivity
bridg:PlannedActivity
urn:LabViewer2.2:SpecimenCollection.plannedIndicator
bridg:PlannedActivity
urn:LabViewer2.2:Activity.plannedIndicator
bridg:PlannedActivity
urn:PSCv2.6:PlannedActivity
bridg:PlannedActivity
urn:PSCv2.6:Period
bridg:PlannedActivity
urn:PSCv2.6:StudySegment
bridg:PlannedActivity
urn:SDTM_IGv3.1.2:TI.DOMAIN
bridg:PlannedCompositionRelationship
PlannedCompositionRelationship
bridg:PlannedCompositionRelationship
false
bridg:PlannedCompositionRelationship
A relationship between a composite activity and a component activity that comprises it, i.e. parent and child activities where all activities are intended to occur at some point in the context of a particular study.
bridg:PlannedCompositionRelationship
A battery of tests may be composed of multiple routine labs that are always ordered together as a group.
bridg:PlannedCompositionRelationship
A glucose tolerance test which is comprised of administering glucose and taking multiple timed blood samples which are then tested for glucose.
bridg:PlannedCompositionRelationship
This class helps represent an AND relationship between siblings with the same parent activity.
bridg:PlannedCompositionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:PlannedCompositionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:PlannedCompositionRelationship
urn:CTRv1.0:PlannedCompositionRelationship
bridg:PlannedCompositionRelationship
urn:HL7SD:PlannedActivity.precondition1.conjunctionCode
bridg:PlannedCompositionRelationship
urn:HL7SD:EligibilityCriterion.Precondition2.conjunctionCode
bridg:PlannedCompositionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:PlannedCompositionRelationship
urn:TDM:TriggeringRule
bridg:PlannedContingentOnRelationship
PlannedContingentOnRelationship
bridg:PlannedContingentOnRelationship
false
bridg:PlannedContingentOnRelationship
A relationship between a planned activity and some criteria to determine if the activity should occur where all activities are intended to occur at some point in the context of a particular study.
bridg:PlannedContingentOnRelationship
Only perform a certain lab test if drug X was administered. (target = another activity)
bridg:PlannedContingentOnRelationship
Only perform a substance administration of drug X if the blood pressure was over some threshold number. (target = observation result from another activity that is an observation)
bridg:PlannedContingentOnRelationship
Only perform a substance administration of drug Y if the blood pressure was over some threshold number and either the result of a certain lab test was positive or the subject's temperature was elevated
bridg:PlannedContingentOnRelationship
i.e. "(A and (B or C))".
bridg:PlannedContingentOnRelationship
The criteria may be one of the following:
- another planned activity where the source activity does not occur unless the target activity has occurred
- the defined outcome of another planned activity where the source activity does not occur unless the target activity outcome has occurred
- a planned group of other criteria that may be composed of a mix of other activities, observation results and/or other groups
To evaluate whether the contingency was satisfied, the simple existence of a PerformedActivity (or subclass) related to the DefinedActivity (or subclass) is not enough by itself. The PerformedActivity.statusCode and PerformedActivity.negationIndicator must also be checked to ensure that the activity was actually performed. PerformedActivity.statusCode must be "Completed" and PerformedActivity.negationIndicator must not be "true".
be contingent upon Exclusive Or
bridg:PlannedContingentOnRelationship
A PlannedContingentOnRelationship must be associated to one and only one of the following: PlannedActivity, DefinedObservationResult, PlannedCriterionGroup.
completionRequiredIndicator Qualifier
bridg:PlannedContingentOnRelationship
completionRequiredBeforeStartingIndicator may only be used if the target of this relationship is an activity, not if the target is an observation result or a criterion group.
bridg:PlannedContingentOnRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:PlannedContingentOnRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:PlannedContingentOnRelationship
urn:CTRv1.0:PlannedContingentOnRelationship
bridg:PlannedContingentOnRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:PlannedContingentOnRelationship
urn:TDM:TriggeringRule
bridg:PlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedCriterionGroup
false
bridg:PlannedCriterionGroup
A collection of conditions joined together via composition (ANDed) and/or optionality (ORed) to form a logical expression upon which the execution of an activity is based or upon which the cessation of a repeated activity is based, where components of the group may include other activities, observation results and/or other criterion groups, and where both the criterion group and its components are planned to be used at a particular point in a particular study.
bridg:PlannedCriterionGroup
(A and (B or C))
bridg:PlannedCriterionGroup
where A might be an activity
bridg:PlannedCriterionGroup
B and C might be 2 different observation results
bridg:PlannedCriterionGroup
and the two sets of parentheses are 2 criterion groups
bridg:PlannedCriterionGroup
one inside (a component of) the other.
bridg:PlannedCriterionGroup
A criterion group represents the parentheses around a set of criteria in a logical expression.
bridg:PlannedCriterionGroup
urn:CTRv1.0:PlannedCriterionGroup
bridg:PlannedCriterionGroup
urn:TDMv2:PlannedCriterionGroup
bridg:PlannedCriterionGroupCompositionRelationship
PlannedCriterionGroupCompositionRelationship
bridg:PlannedCriterionGroupCompositionRelationship
false
bridg:PlannedCriterionGroupCompositionRelationship
A relationship between a planned criterion group and a planned activity, planned observation result or other planned criterion group that is a component, i.e. a relationship between a logical set of parenthesis and one of the items inside the parentheses.
bridg:PlannedCriterionGroupCompositionRelationship
A battery of tests may be composed of multiple routine labs that are always ordered together as a group.
bridg:PlannedCriterionGroupCompositionRelationship
A glucose tolerance test which is comprised of administering glucose and taking multiple timed blood samples which are then tested for glucose.
bridg:PlannedCriterionGroupCompositionRelationship
This class helps represent an AND relationship between siblings in the same criterion group.
be the parent of Exclusive Or
bridg:PlannedCriterionGroupCompositionRelationship
A PlannedCriterionGroupCompositionRelationship must be associated to one and only one of the following targets: PlannedActivity, DefinedObservationResult, PlannedCriterionGroup.
bridg:PlannedCriterionGroupCompositionRelationship
urn:CTGOV:ActivityRelationship.typeCode
bridg:PlannedCriterionGroupCompositionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:PlannedCriterionGroupCompositionRelationship
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship
bridg:PlannedCriterionGroupCompositionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:PlannedCriterionGroupCompositionRelationship
urn:TDM:TriggeringRule
bridg:PlannedCriterionGroupOptionRelationship
PlannedCriterionGroupOptionRelationship
bridg:PlannedCriterionGroupOptionRelationship
false
bridg:PlannedCriterionGroupOptionRelationship
A relationship between a planned criterion group and an option that can satisfy it, either a planned activity, a planned observation result or another planned criterion group, i.e. a relationship between a logical set of parenthesis and one of the options inside the parentheses.
bridg:PlannedCriterionGroupOptionRelationship
A pain management criterion group may be comprised of three options
bridg:PlannedCriterionGroupOptionRelationship
one for substance administration of Tylenol
bridg:PlannedCriterionGroupOptionRelationship
another for substance administration of aspirin
bridg:PlannedCriterionGroupOptionRelationship
and a third for substance administration of ibuprofen. The pain management criterion would be satisfied/accomplished with any one of these activities and would be associated to each of the three via a different DefinedCriterionGroupOptionRelationship.
bridg:PlannedCriterionGroupOptionRelationship
This class helps represent an OR relationship between siblings in the same criterion group.
is a choice that has as option Exclusive Or
bridg:PlannedCriterionGroupOptionRelationship
A PlannedCriterionGroupOptionRelationship must be associated to one and only one of the following targets: PlannedActivity, DefinedObservationResult, PlannedCriterionGroup.
bridg:PlannedCriterionGroupOptionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:PlannedCriterionGroupOptionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:PlannedCriterionGroupOptionRelationship
urn:CTRv1.0:PlannedCriterionGroupOptionRelationship
bridg:PlannedCriterionGroupOptionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:PlannedCriterionGroupOptionRelationship
urn:TDM:TriggeringRule
bridg:PlannedEligibilityCriterion
PlannedEligibilityCriterion
bridg:PlannedEligibilityCriterion
true
bridg:PlannedEligibilityCriterion
An activity that is intended to occur at some point in the context of a particular study that represents a characteristic or requirement intended to be applied to a potential study subject to determine whether or not they may participate in a study.
bridg:PlannedEligibilityCriterion
The reason for the PlannedEligibilityCriterion structure is to allow questions defined as agnostic criteria in DefinedEligibilityCriterion, that is, they could be used either as inclusion or exclusion criteria, to be referenced in specific study protocols and allow the inclusion/exclusion distinction to be determined for that study specifically.
bridg:PlannedEligibilityCriterion
urn:CTRPv3.8:PlannedEligibilityCriterion
bridg:PlannedExclusionCriterion
PlannedExclusionCriterion
bridg:PlannedExclusionCriterion
false
bridg:PlannedExclusionCriterion
An activity that is intended to occur at some point in the context of a particular study that represents a characteristic or requirement intended to be applied to a potential study subject to determine whether they may not participate in a study.
bridg:PlannedExclusionCriterion
The reason for the PlannedEligibilityCriterion structure is to allow questions defined as agnostic criteria in DefinedEligibilityCriterion, that is, they could be used either as inclusion or exclusion criteria, to be referenced in specific study protocols and allow the inclusion/exclusion distinction to be determined for that study specifically.
bridg:PlannedInclusionCriterion
PlannedInclusionCriterion
bridg:PlannedInclusionCriterion
false
bridg:PlannedInclusionCriterion
An activity that is intended to occur at some point in the context of a particular study that represents a characteristic or requirement intended to be applied to a potential study subject to determine whether they may participate in a study.
bridg:PlannedInclusionCriterion
The reason for the PlannedEligibilityCriterion structure is to allow questions defined as agnostic criteria in DefinedEligibilityCriterion, that is, they could be used either as inclusion or exclusion criteria, to be referenced in specific study protocols and allow the inclusion/exclusion distinction to be determined for that study specifically.
bridg:PlannedInclusionCriterion
urn:CTRPv3.8:PlannedEligibilityCriterion.inclusionIndicator
bridg:PlannedNotification
PlannedNotification
bridg:PlannedNotification
false
bridg:PlannedNotification
An activity that is intended to occur at some point in the context of a particular study that represents the communication of a message to a recipient.
Accrual Threshold Percent Exclusive Or
bridg:PlannedNotification
A PlannedNotification may have a value for one and only one for the following: studyAccrualThresholdPercent or studySiteAccrualThresholdPercent.
be participated in by Qualifier
bridg:PlannedNotification
Associations from Subject (including StudySubject) are valid. Associations from ExperimentalUnit are not valid.
be received by actualIndicator Qualifier
bridg:PlannedNotification
Only Organization or Person (via NotificationReceiver) with actualIndicator = "false" is valid.
bridg:PlannedNotification
urn:C3PRv2.9:PlannedNotification
bridg:PlannedOptionRelationship
PlannedOptionRelationship
bridg:PlannedOptionRelationship
false
bridg:PlannedOptionRelationship
A relationship between a composite activity and an option that can satisfy it, i.e. choice and option activities, where all the activities are intended to occur at some point in the context of a particular study.
bridg:PlannedOptionRelationship
A pain management activity may be comprised of three options
bridg:PlannedOptionRelationship
one for substance administration of Tylenol
bridg:PlannedOptionRelationship
another for substance administration of aspirin
bridg:PlannedOptionRelationship
and a third for substance administration of ibuprofen. The pain management activity would be satisfied/accomplished with any one of these activities and would be associated to each of the three via a different DefinedOptionRelationship.
bridg:PlannedOptionRelationship
This class helps represent an OR relationship between siblings with the same parent activity.
bridg:PlannedOptionRelationship
urn:CTOM:ActivityRelationship.typeCode
bridg:PlannedOptionRelationship
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:PlannedOptionRelationship
urn:CTRv1.0:PlannedOptionRelationship
bridg:PlannedOptionRelationship
urn:HL7SD:EligibilityCriterion.Precondition2.conjunctionCode
bridg:PlannedOptionRelationship
urn:HL7SD:PlannedActivity.precondition1.conjunctionCode
bridg:PlannedOptionRelationship
urn:TDM:AbstractRule.evaluableExpression
bridg:PlannedOptionRelationship
urn:TDM:TriggeringRule
bridg:PlannedRandomizationBookAllocation
PlannedRandomizationBookAllocation
bridg:PlannedRandomizationBookAllocation
false
bridg:PlannedRandomizationBookAllocation
An activity that is intended to occur at some point in the context of a particular study and that is the assignment of an experimental unit to a portion of the study, such as an arm or a portion of an arm (when secondary allocations may occur) based on a randomization book.
bridg:PlannedRandomizationBookAllocation
A randomization book is a predefined set of assignments to portions of a study based on criteria, such as stratum group for example, that ensures a desired distribution of experimental units across those portions of the study. For example, the book entries indicate which arm a given experimental unit, Joe, is assigned to based on the fact that he's the 5th person in stratum group #2.
DefinedActivity Qualifier
bridg:PlannedRandomizationBookAllocation
A PlannedRandomizationBookAllocation can only reference a StudyActivity that points to DefinedExperimentalUnitAllocation, not any other DefinedActivity subclass.
Repeat Not Applicable
bridg:PlannedRandomizationBookAllocation
The Repeat attributes should not be used for a PlannedRandomizationBookAllocation.
be participated in by Qualifier
bridg:PlannedRandomizationBookAllocation
Associations from ExperimentalUnit are valid. Associations from Subject (including StudySubject) are not valid.
bridg:PlannedRandomizationBookAllocation
urn:C3PR:BookRandomization
bridg:PlannedRandomizationBookAllocation
urn:C3PRv2.9:BookRandomization
bridg:PlannedRandomizationBookAllocation
urn:CTRRr3:PlannedRandomizationBookAllocation
bridg:PlannedRepeatActivityUntilRule
PlannedRepeatActivityUntilRule
bridg:PlannedRepeatActivityUntilRule
false
bridg:PlannedRepeatActivityUntilRule
A relationship between a planned repeating activity and the criteria that may trigger the repeating activity to stop, where all items are intended to occur at some point in the context of a particular study.
bridg:PlannedRepeatActivityUntilRule
Continue repeating kidney dialysis until kidney transplant surgery.
bridg:PlannedRepeatActivityUntilRule
The criteria may be one of the following:
- another planned activity where the repeating activity stops if this other activity occurs
- a defined observation result where the repeating activity stops if this observation result occurs as a result of a planned observation
- a planned criteria group where the repeating activity stops if this group logically evaluates to true based on its components
be repeated until Exclusive Or
bridg:PlannedRepeatActivityUntilRule
A PlannedRepeatActivityUntilRule must be associated to one and only one of the following: PlannedActivity, DefinedObservationResult, PlannedCriterionGroup.
bridg:PlannedRepeatActivityUntilRule
urn:CTOM:ActivityRelationship.typeCode
bridg:PlannedRepeatActivityUntilRule
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:PlannedRepeatActivityUntilRule
urn:CTRv1.0:PlannedRepeatActivityUntilRule
bridg:PlannedRepeatActivityUntilRule
urn:TDM:TriggeringRule
bridg:PlannedRepeatActivityUntilRule
urn:TDM:AbstractRule.evaluableExpression
bridg:PlannedStudySite
PlannedStudySite
bridg:PlannedStudySite
false
bridg:PlannedStudySite
A facility in which study activities are intended to be conducted.
bridg:PlannedStudySite
The site where the study subject encounter is intended to occur
bridg:PlannedStudySite
or the site of the Investigator.
be a function planned to be performed by Exclusive Or
bridg:PlannedStudySite
A PlannedStudySite is a function planned to be performed by one and only one of the following: HealthcareFacility, Organization (serving as a PlannedStudySite but is not a HealthcareFacility).
bridg:PlannedStudySite
urn:BRIDGSCC:Model_Integrity_-_Study_Versioning
bridg:PlannedStudySite
urn:CTRv1.0:PlannedStudySite
bridg:PlannedStudySubject
PlannedStudySubject
bridg:PlannedStudySubject
false
bridg:PlannedStudySubject
A kind of physical entity which is intended to be the primary unit of operational and/or administrative interest in a study.
bridg:PlannedStudySubject
10 Adult males
bridg:PlannedStudySubject
20 female 6-month old chickens
bridg:PlannedStudySubject
Some studies may specify multiple kinds of subjects, each with their own quantity.
be a function performed by actualIndicator Qualifier
bridg:PlannedStudySubject
Only BiologicEntity, Material (via Subject) with actualIndicator = "false" is valid.
bridg:PlannedStudySubject
urn:CTRv1.0:PlannedSubject
bridg:PlannedSubjectActivityGroup
PlannedSubjectActivityGroup
bridg:PlannedSubjectActivityGroup
false
bridg:PlannedSubjectActivityGroup
A collection of activities that are intended to occur or start for the same study subject at a specific point in the context of a particular study.
bridg:PlannedSubjectActivityGroup
Clinic visit during which a physical exam
bridg:PlannedSubjectActivityGroup
a blood test
bridg:PlannedSubjectActivityGroup
and a substance administration occur
bridg:PlannedSubjectActivityGroup
Telephone contact during which temperature
bridg:PlannedSubjectActivityGroup
blood pressure and adverse events are reported
bridg:PlannedSubjectActivityGroup
Recording multiple observation results in a diary
bridg:PlannedSubjectActivityGroup
A treatment strategy that consists of drug administrations with rules for modifying doses
bridg:PlannedSubjectActivityGroup
visit
bridg:PlannedSubjectActivityGroup
time point
bridg:PlannedSubjectActivityGroup
study segment
bridg:PlannedSubjectActivityGroup
course
bridg:PlannedSubjectActivityGroup
treatment strategy
bridg:PlannedSubjectActivityGroup
period
bridg:PlannedSubjectActivityGroup
cycle
be participated in by Qualifier
bridg:PlannedSubjectActivityGroup
Associations from Subject are valid only for StudySubject. Associations from ExperimentalUnit are not valid.
bridg:PlannedSubjectActivityGroup
urn:CTRv1.0:PlannedSubjectActivityGroup
bridg:PlannedSubjectActivityGroup
urn:SDTM_IGv3.1.2:TE.DOMAIN
bridg:PlannedSubjectActivityGroup
urn:SDTM_IGv3.1.2:TV.DOMAIN
bridg:PrincipalStatisticalAnalysisPlanVersion
PrincipalStatisticalAnalysisPlanVersion
bridg:PrincipalStatisticalAnalysisPlanVersion
false
bridg:PrincipalStatisticalAnalysisPlanVersion
A type of statistical analysis plan that is the main, comprehensive, pre-specified collection of analyses that support the Clinical Study Report (CSR) or other similar study report.
bridg:PrincipalStatisticalAnalysisPlanVersion
Analyses that arise after PrincipalStatisticalAnalysisPlanVersion finalization but during preparation of the clinical study report are handled by SupplementalStatisticalAnalysisPlanVersion.
bridg:PrincipalStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:PrincipalStatisticalAnalysisPlanVersion
bridg:ProcessedProduct
ProcessedProduct
bridg:ProcessedProduct
false
bridg:ProcessedProduct
Specifies the link between a processor and a product produced by that processor.
bridg:ProcessedProduct
urn:CTRv1.0:ProcessedProduct
in R_Product
bridg:ProcessedProduct
urn:ICSRr2:ManufacturedProduct2
bridg:ProcessingSite
ProcessingSite
bridg:ProcessingSite
false
bridg:ProcessingSite
The particular plant or processing location at which the product was processed
bridg:ProcessingSite
GSK Zebulon
bridg:ProcessingSite
NC
bridg:ProcessingSite
The site could pertain to a different corporation than the one which is the formal manufacturer.
bridg:ProcessingSite
urn:AE:ManufacturingSite
bridg:Processor
Processor
bridg:Processor
false
bridg:Processor
An organization defined as being responsible for making, assembling, refurbishing, packaging, etc. a product.
bridg:Processor
The maker identified on the product's box.
bridg:Processor
In some cases, the responsible organization will actually be listed as a reprocessor of the item.
bridg:Processor
urn:AE:Manufacturer
bridg:Processor
urn:CTRv1.0:Processor
bridg:Product
Product
bridg:Product
false
bridg:Product
A thing produced by or resulting from a process.
bridg:Product
drug
bridg:Product
device
bridg:Product
animal and human drugs; therapeutic biologics; allergenics; cell
bridg:Product
tissue and gene therapy products; blood components; blood derivative products; devices; animal (pets and livestock) and human food/feed (medicated and un-medicated); cosmetics; pet treats; dietary supplements [examples from FDA's list of regulated products]
Attribute Set actualIndicator Qualifier
bridg:Product
effectiveDateRange, codeModifiedText, lotNumberText, expirationDate are valid only when actualIndicator = "true".
Distributor Qualifier
bridg:Product
If Product.actualIndicator = "true", then the upper limit is 1 on the Distributor association.
ProcessingSite Qualifier
bridg:Product
If Product.actualIndicator = "true", then the upper limit is 1 on the ProcessingSite association.
Processor Qualifier
bridg:Product
If Product.actualIndicator = "true", then the upper limit is 1 on the Processor association.
bridg:Product
urn:AE:Component
bridg:Product
urn:AE:Product
bridg:Product
urn:AE:Ingredient
bridg:Product
urn:CTRPv1.0:Product
bridg:Product
urn:CTRRr3:Product
bridg:Product
urn:CTRv1.0:Product
bridg:Product
urn:HL7SD:Product
bridg:Product
urn:HL7SP:Product
in R_Product
bridg:Product
urn:ICSRr2:Substance
in R_Product
bridg:Product
urn:ICSRr2:Container
in R_Product
bridg:Product
urn:ICSRr2:InstanceOfKind
in R_Product
bridg:Product
urn:ICSRr2:ManufacturedProduct
in A_ProductReportingRelevantInformation
bridg:Product
urn:ICSRr2:product
in R_Product
bridg:Product
urn:ICSRr2:Product
in R_Product
bridg:Product
urn:ICSRr2:ProductInstance
bridg:Product
urn:caAERSv2.2:Agent
bridg:Product
urn:caAERSv2.2:StudyParticipantPriorTherapyAgent
bridg:Product
urn:caAERSv2.2:PriorTherapyAgent
bridg:Product
urn:caAERSv2.2:ConcomitantMedication
bridg:Product
urn:caAERSv2.2:CourseAgent
bridg:ProductGroup
ProductGroup
bridg:ProductGroup
false
bridg:ProductGroup
A collection of instances of a product.
bridg:ProductGroup
10 pills
bridg:ProductGroup
5 pace makers
Attribute Set actualIndicator Qualifier
bridg:ProductGroup
identifier is valid only when actualIndicator = "true".
bridg:ProductGroup
urn:HL7SD:GroupKind
bridg:ProductRelationship
ProductRelationship
bridg:ProductRelationship
false
bridg:ProductRelationship
Specifies the link between one product and another.
bridg:ProductRelationship
lot
bridg:ProductRelationship
content
bridg:ProductRelationship
kind
bridg:ProductRelationship
part
bridg:ProductRelationship
ingredient
bridg:ProductRelationship
package
bridg:ProductRelationship
assembly
bridg:ProductRelationship
specialized
bridg:ProductRelationship
equivalent
identifier Qualifier
bridg:ProductRelationship
identifier is only valid when Product.actualIndicator = "false".
bridg:ProductRelationship
urn:BRIDGSCC:Model_Integrity
bridg:ProductRelationship
urn:CTRRr3:ProductPart
bridg:ProductRelationship
urn:CTRv1.0:ProductRelationship
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Member1
in R_Product
bridg:ProductRelationship
urn:ICSRr2:EquivalentSubstance
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Content3
in R_Product
bridg:ProductRelationship
urn:ICSRr2:PartOfAssembly
in R_Product
bridg:ProductRelationship
urn:ICSRr2:InstanceOfKind2
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Content1
in R_Product
bridg:ProductRelationship
urn:ICSRr2:ingredient1
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Member
in R_Product
bridg:ProductRelationship
urn:ICSRr2:SpecializedKind
in R_Product
bridg:ProductRelationship
urn:ICSRr2:part1
in R_Product
bridg:ProductRelationship
urn:ICSRr2:EquivalentEntity
in R_Product
bridg:ProductRelationship
urn:ICSRr2:part
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Ingredient
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Content
in R_Product
bridg:ProductRelationship
urn:ICSRr2:Content2
bridg:QualifiedPerson
QualifiedPerson
bridg:QualifiedPerson
false
bridg:QualifiedPerson
A person that has been recognized as having certain training/experience or other characteristics that would make that person an appropriate performer for a certain activity.
bridg:QualifiedPerson
board certification
bridg:QualifiedPerson
academic degree
bridg:QualifiedPerson
medical license
Mandatory Attribute Qualifier
bridg:QualifiedPerson
At least one of the following attributes must be mandatory for a QualifiedPerson: typeCode, certificateLicenseText.
bridg:QualifiedPerson
urn:CTGOV:Investigators_-_Degrees
bridg:QualifiedPerson
urn:CTGOV:Overall_State_Officials_-_Degree
bridg:QualifiedPerson
urn:CTGOV:Central_Contact_-_Degrees
bridg:QualifiedPerson
urn:CTGOV:Facility_Contact_-_Degree
bridg:QualifiedPerson
urn:CTRv1.0:QualifiedPerson
in IndividualCaseSafetyReport
bridg:QualifiedPerson
urn:ICSRr2:QualifiedEntity
bridg:RandomizationBookEntry
RandomizationBookEntry
bridg:RandomizationBookEntry
false
bridg:RandomizationBookEntry
An item/element of a randomization book that can be used to assign an experimental unit to a planned arm or portion of an arm in a study.
bridg:RandomizationBookEntry
An entry might be mapping the 5th experimental unit in a given Stratum Group to a particular treatment Arm.
bridg:RandomizationBookEntry
A randomization book is a predefined set of assignments to portions of a study based on criteria, such as stratum group for example, that ensures a desired distribution of experimental units across those portions of the study. For example, the book entries indicate which arm a given experimental unit, Joe, is assigned to based on the fact that he's the 5th experimental unit in stratum group #2.
bridg:RandomizationBookEntry
urn:C3PRv2.9:BookRandomizationEntry
bridg:RandomizationBookEntry
urn:CTRRr3:RandomizationBookEntry
bridg:ReferenceResult
ReferenceResult
bridg:ReferenceResult
false
bridg:ReferenceResult
The possible or expected results that can be obtained by observing, monitoring, measuring or otherwise qualitatively or quantitatively recording one or more aspects of physiologic or psychologic processes.
bridg:ReferenceResult
The normal range for a systolic blood pressure reading is 110-130 for adult males:
bridg:ReferenceResult
ReferenceResult.referenceTypeCode = normal range
bridg:ReferenceResult
ReferenceResult.valueTypeCode = systolic blood pressure
bridg:ReferenceResult
ReferenceResult.value(ANY=>IVL<PQ>) = 110-130 mm[Hg]
bridg:ReferenceResult
ReferenceResult.populationScopeCode = adult males
bridg:ReferenceResult
The limit of quantitation for a PK assay
bridg:ReferenceResult
concentration of drug XYZ is 2-60 nanograms/ml for adult women as processed by Acme Labs:
bridg:ReferenceResult
ReferenceResult.referenceTypeCode = limit of quantitation
bridg:ReferenceResult
ReferenceResult.valueTypeCode = PK assay
bridg:ReferenceResult
concentration of drug XYZ
bridg:ReferenceResult
ReferenceResult.value(ANY=>IVL<PQ>) = 2-60 nanograms/ml
bridg:ReferenceResult
ReferenceResult > PerformingLaboratory > Laboratory > Organization.name = Acme Labs
bridg:ReferenceResult
The normal range for a hemoglobin concentration measurement on an adult female performed by Acme Labs is 12.1 to 15.1 g/dL:
bridg:ReferenceResult
ReferenceResult.referenceTypeCode = normal range
bridg:ReferenceResult
ReferenceResult.valueTypeCode = hemoglobin concentration measurement
bridg:ReferenceResult
ReferenceResult.value(ANY=>IVL<PQ>) = 12.1 to 15.1 g/dL
bridg:ReferenceResult
ReferenceResult.populationScopeCode = adult females
bridg:ReferenceResult
ReferenceResult > PerformingLaboratory > Laboratory > Organization.name = Acme Labs
bridg:ReferenceResult
The normal range for a fasting blood glucose measurement on an adult performed by Acme Labs is 3.6 to 5.8 mmol/L:
bridg:ReferenceResult
ReferenceResult.referenceTypeCode = normal range
bridg:ReferenceResult
ReferenceResult.valueTypeCode = blood glucose measurement
bridg:ReferenceResult
ReferenceResult.value(ANY=>IVL<PQ>)= 3.6 to 5.8 mmol/L
bridg:ReferenceResult
ReferenceResult.populationScopeCode = adult
bridg:ReferenceResult
ReferenceResult.fastingStatusIndicator = true
bridg:ReferenceResult
ReferenceResult > PerformingLaboratory > Laboratory > Organization.name = Acme Labs
bridg:ReferenceResult
Normal range
bridg:ReferenceResult
reference range
bridg:ReferenceResult
limit of quantitation
bridg:ReferenceResult
clinical concern range
bridg:ReferenceResult
data checking range
bridg:ReferenceResult
alert range
bridg:ReferenceResult
The context of a reference result may include any combination of the following: the performing lab, the performing device, and the population to which the reference value pertains. The context may also omit any of those aspects as well.
apply to results produced by actualIndicator Qualifier
bridg:ReferenceResult
Only Device or Organization (via PerformingLaboratory) with actualIndicator = "true" is valid.
bridg:ReferenceResult
urn:BRIDGSCC:Model_Integrity
bridg:ReferenceResult
urn:CTRv1.0:ReferenceResult
bridg:ReferenceToStudyResults
ReferenceToStudyResults
bridg:ReferenceToStudyResults
false
bridg:ReferenceToStudyResults
A citation in an external publication that refers to results of this study.
bridg:ReferenceToStudyResults
CT.gov instruction say to provide either the unique PubMed Identifier (PMID) of an article or enter the full bibliographic citation.
"Inbound" references, could be to interim or final results, not a reference from this study to other studies.
bridg:ReferenceToStudyResults
urn:CTRv1.0:ReferenceToStudyResults
bridg:RegistrationCenter
RegistrationCenter
bridg:RegistrationCenter
false
bridg:RegistrationCenter
The service of recording subject participation on a study. The service may include allocation to an Arm or a portion of an Arm (when secondary allocations may occur).
bridg:RegistrationCenter
urn:CTRv1.0:RegistrationCenter
bridg:RegulatoryApplication
RegulatoryApplication
bridg:RegulatoryApplication
false
bridg:RegulatoryApplication
A collection of submissions that are grouped together for regulatory purposes, and are usually specific to a particular device, food or feed additive or biopharmaceutical substance.
bridg:RegulatoryApplication
The marketing application for a drug product can generate multiple regulatory decisions. The first decision may support the initial marketing approval of the product for a specific indication. Subsequent regulatory decisions may approve or deny additional indications for the drug product. The application thus contains multiple submissions
bridg:RegulatoryApplication
each with their own regulatory action.
bridg:RegulatoryApplication
Over time, an application will typically consist of multiple submissions and regulatory assessments.
bridg:RegulatoryApplication
urn:CTRPv3.8:StudyIndIde
bridg:RegulatoryApplication
urn:CTRRr3:RegulatoryApplication
bridg:RegulatoryApplication
urn:CTRv1.0:RegulatoryApplication
bridg:RegulatoryApplication
urn:RPS1:Application
bridg:RegulatoryApplication
urn:caAERSv2.2:InvestigationalNewDrug
bridg:RegulatoryApplicationSponsor
RegulatoryApplicationSponsor
bridg:RegulatoryApplicationSponsor
false
bridg:RegulatoryApplicationSponsor
An organization or person that assumes responsibility for producing and submitting documentation to a regulatory authority to seek approval for testing, marketing and the continuation of marketing of new drugs or devices.
bridg:RegulatoryApplicationSponsor
pharmaceutical company
be a function performed by Exclusive Or
bridg:RegulatoryApplicationSponsor
A RegulatoryApplicationSponsor might be a function performed by one and only one of the following: Organization, HealthcareProvider.
be a function performed by actualIndicator Qualifier
bridg:RegulatoryApplicationSponsor
Only Organization with actualIndicator = "true" is valid.
bridg:RegulatoryApplicationSponsor
urn:CTRPv1.0:RegulatoryApplicationSponsor
bridg:RegulatoryApplicationSponsor
urn:CTRRr3:RegulatoryApplicationSponsor
bridg:RegulatoryApplicationSponsor
urn:CTRv1.0:RegulatoryApplicationSponsor
in R_Product
bridg:RegulatoryApplicationSponsor
urn:ICSRr2:holder
in R_Product
bridg:RegulatoryApplicationSponsor
urn:ICSRr2:role
bridg:RegulatoryApplicationSponsor
urn:caAERSv2.2:INDHolder
bridg:RegulatoryAssessment
RegulatoryAssessment
bridg:RegulatoryAssessment
false
bridg:RegulatoryAssessment
An evaluation of a submission by a regulatory body.
bridg:RegulatoryAssessment
The FDA evaluates a submission for a new drug or device.
is a function performed by actualIndicator Qualifier
bridg:RegulatoryAssessment
Only Organization (via OversightAuthority) with actualIndicator = "true" is valid.
bridg:RegulatoryAssessment
urn:AE:Authorization
bridg:RegulatoryAssessment
urn:CTRRr3:RegulatoryAssessment
bridg:RegulatoryAssessment
urn:CTRv1.0:RegulatoryAssessment
in R_Product
bridg:RegulatoryAssessment
urn:ICSRr2:Approval
bridg:RegulatoryAuthority
RegulatoryAuthority
bridg:RegulatoryAuthority
false
bridg:RegulatoryAuthority
Governmental bodies that have the power to pass and enforce laws.
bridg:RegulatoryAuthority
Medicines and Healthcare Products Regulatory Agency (MHRA) in the UK
bridg:RegulatoryAuthority
Food and Drug Administration (FDA) in the USA
bridg:RegulatoryAuthority
urn:AE:RegulatoryAuthority
bridg:RegulatoryAuthority
urn:CTRPv1.0:RegulatoryAuthority
bridg:RegulatoryAuthority
urn:CTRPv3.8:RegulatoryAuthority
bridg:RegulatoryAuthority
urn:CTRRr3:RegulatoryAuthority
bridg:RegulatoryAuthority
urn:CTRv1.0:RegulatoryAuthority
in R_Product
bridg:RegulatoryAuthority
urn:ICSRr2:territorialAuthority
in R_Product
bridg:RegulatoryAuthority
urn:ICSRr2:Author2
bridg:RelevantRegulation
RelevantRegulation
bridg:RelevantRegulation
false
bridg:RelevantRegulation
Specifies the jurisdictional law that may be applicable for registering the study to a clinical trial registry.
bridg:ReportReceiver
ReportReceiver
bridg:ReportReceiver
false
bridg:ReportReceiver
A role of a person or an organization that receives or is intended to receive a report..
be a function performed by Exclusive Or
bridg:ReportReceiver
A ReportReceiver might be a function performed by one and only one of the following: Person, Organization.
bridg:ReportReceiver
urn:AE:Receiver
bridg:ReportReceiver
urn:CTRv1.0:ReportReceiver
in IndividualCaseSafetyReport
bridg:ReportReceiver
urn:ICSRr2:AssignedEntity
in IndividualCaseSafetyReport
bridg:ReportReceiver
urn:ICSRr2:Participant1
in IndividualCaseSafetyReport
bridg:ReportReceiver
urn:ICSRr2:PrimaryInformationRecipient
in IndividualCaseSafetyReport
bridg:ReportReceiver
urn:ICSRr2:AssignedEntity.code
in IndividualCaseSafetyReport
bridg:ReportReceiver
urn:ICSRr2:LocatedEntity
in IndividualCaseSafetyReport
bridg:ReportReceiver
urn:ICSRr2:LocatedEntity2
bridg:ReportReceiver
urn:caAERSv2.2:ReportDelivery
bridg:ReportSubmitter
ReportSubmitter
bridg:ReportSubmitter
false
bridg:ReportSubmitter
A role of a person who submits a report.
bridg:ReportSubmitter
urn:CTRv1.0:ReportSubmitter
bridg:ReportSubmitter
urn:caAERSv2.2:RoleBasedRecipient.role
bridg:ReportSubmitter
urn:caAERSv2.2:Submitter
bridg:ReportVersion
ReportVersion
bridg:ReportVersion
false
bridg:ReportVersion
A document characterized by information or other content which is tailored to the context of a given situation and audience.
bridg:ReportVersion
Safety Report
bridg:ReportVersion
Study Report
bridg:ReportVersion
urn:AE:ReportReceipt
bridg:ReportVersion
urn:C3PRv2.9:ReportVersion
bridg:ReportVersion
urn:CTRRr3:Report
bridg:ReportVersion
urn:CTRv1.0:ReportVersion
bridg:ReportVersion
urn:caAERSv2.2:Report
bridg:Reprocessor
Reprocessor
bridg:Reprocessor
false
bridg:Reprocessor
An organization that is typically in the business of re-using or refurbishing a product (such as a medical device) so that it can be used again. These kind of organizations must comply with the same requirements that apply to original equipment manufacturers.
bridg:Reprocessor
These organizations are typically referred to as third part or hospital reprocessors. Reprocessing of medical devices is done to save costs and reduce wastes.
bridg:Reprocessor
urn:CTRv1.0:Reprocessor
bridg:ResearchOrganization
ResearchOrganization
bridg:ResearchOrganization
false
bridg:ResearchOrganization
An organization whose purpose is to support systemic, rigorous study and investigation into a particular field or fields.
bridg:ResearchOrganization
Clinical Research Organization (CRO)
bridg:ResearchOrganization
urn:AE:ResearchInstitution
bridg:ResearchOrganization
urn:CTRPv1.0:ResearchOrganization
bridg:ResearchOrganization
urn:CTRPv3.8:ResearchOrganization
bridg:ResearchOrganization
urn:CTRv1.0:ResearchOrganization
bridg:ResearchStaff
ResearchStaff
bridg:ResearchStaff
false
bridg:ResearchStaff
Individual who is employed and/or involved in any aspect of conduct of protocol driven research.
bridg:ResearchStaff
administrators
bridg:ResearchStaff
clinical and data managers
bridg:ResearchStaff
clinical research pharmacists
bridg:ResearchStaff
clinical research associates
bridg:ResearchStaff
clinical trials compliance coordinators
bridg:ResearchStaff
clinical trials specialists
bridg:ResearchStaff
laboratory technologists
bridg:ResearchStaff
nurses
bridg:ResearchStaff
research services consultants
bridg:ResearchStaff
study coordinators and others
Person-ResearchOrganization Pair Unique
bridg:ResearchStaff
Each Person can have more than one ResearchStaff role but each of them must be for a different ResearchOrganization (no duplicate Person/ResearchOrganization pairs).
bridg:ResearchStaff
urn:C3PRv2.9:ResearchStaff
bridg:ResearchStaff
urn:CTRPv1.0:ClinicalResearchStaff
bridg:ResearchStaff
urn:CTRPv3.8:ClinicalResearchStaff
bridg:ResearchStaff
urn:CTRRr3:ResearchStaff
bridg:ResearchStaff
urn:CTRv1.0:ResearchStaff
bridg:ResearchStaff
urn:caAERSv2.2:SiteResearchStaff
bridg:ResearchStaff
urn:caAERSv2.2:ResearchStaff
bridg:Resource
Resource
bridg:Resource
false
bridg:Resource
Items necessary to support a research study.
bridg:Resource
Funding
bridg:Resource
material
bridg:Resource
labor
bridg:Resource
urn:CTRPv1.0:StudyResourcing
bridg:Resource
urn:CTRRr3:Resource
bridg:Resource
urn:CTRv1.0:Resource
bridg:ResourceProvider
ResourceProvider
bridg:ResourceProvider
false
bridg:ResourceProvider
An organization or person that provides financial or other resources for the conduct of research.
bridg:ResourceProvider
National Cancer Institute
bridg:ResourceProvider
National Institutes of Health [Federal Agency examples]
bridg:ResourceProvider
Pharmaceutical companies [private industry example]
be a function performed by Exclusive Or
bridg:ResourceProvider
A ResourceProvider might be a function performed by one and only one of the following: Organization, Person.
bridg:ResourceProvider
urn:C3PRv2.9:StudyOrganization
bridg:ResourceProvider
urn:CTRPv1.0:ResourceProvider
bridg:ResourceProvider
urn:CTRRr3:ResourceProvider
bridg:ResourceProvider
urn:CTRv1.0:ResourceProvider
bridg:ResourceProvider
urn:HL7SP:Service_Provider
bridg:ResourceProvider
urn:HL7SP:Study.performer2
bridg:ResourceProvider
urn:HSDBv1.0:[Lead_Organization]_.Organization_Type
bridg:ResourceProvider
urn:caAERSv2.2:StudyOrganization
bridg:ReviewableUnit
ReviewableUnit
bridg:ReviewableUnit
false
bridg:ReviewableUnit
A discrete portion of a submission which is used to receive agreement. Once agreement is reached on all units within the submission the submission can then be approved.
bridg:ReviewableUnit
In a Modular pre-marketing application (PMA) several modules will be sent to the Food and Drug Administration (FDA). Each module will be agreed upon independently of other modules. The FDA then approves the submission based on compilation of all of the modules. These modules are reviewable units.
bridg:ReviewableUnit
A veterinary medicine New Animal Drug Application (NADA) (marketing application) is constructed from the Investigational New Animal Drug Application (INADA). In the INADA process the sponsor creates reviewable units. These reviewable units are then compiled to be used as documentation for the marketing application.
bridg:ReviewableUnit
urn:CTRv1.0:ReviewableUnit
bridg:ReviewableUnit
urn:RPS1:ReviewableUnit
bridg:SafetyReportVersion
SafetyReportVersion
bridg:SafetyReportVersion
false
bridg:SafetyReportVersion
A report that provides notification of an adverse event, product problem, and/or information that is relevant to either. A report typically includes causal association, management strategies, authorship, sender/receiver organizations, subject or study subject of adverse event, or name of product.
bridg:SafetyReportVersion
An Expedited AE report - a report of a serious and unexpected adverse event that must be submitted within specific timeframes to the sponsor and regulatory agencies.
describes Exclusive Or
bridg:SafetyReportVersion
A SafetyReportVersion describes one and only one of the following: AdverseEvent, PerformedProductProblemDiscovery.
bridg:SafetyReportVersion
urn:AE:ProductProblemReport
bridg:SafetyReportVersion
urn:AE:NullificationReport
bridg:SafetyReportVersion
urn:AE:SafetyReport
bridg:SafetyReportVersion
urn:CTRRr3:SafetyReport
bridg:SafetyReportVersion
urn:CTRv1.0:SafetyReportVersion
in IndividualCaseSafetyReport
bridg:SafetyReportVersion
urn:ICSRr2:Subject8
in IndividualCaseSafetyReport
bridg:SafetyReportVersion
urn:ICSRr2:Subject9
in IndividualCaseSafetyReport
bridg:SafetyReportVersion
urn:ICSRr2:ControlActEvent
bridg:SafetyReportVersion
urn:caAERSv2.2:ExpeditedAdverseEventReport
bridg:SampleSizeConsideration
SampleSizeConsideration
bridg:SampleSizeConsideration
false
bridg:SampleSizeConsideration
Information needed for computing the sample size, including any detail not provided in the study protocol.
bridg:SampleSizeConsideration
"Approximately 100 patients will be randomized to each of the 3 treatment groups. Previous experience with the oral formulation of xanomeline suggests that this sample size has 90% power to detect a 3.0 mean treatment difference in ADAS-Cog (p<.05
bridg:SampleSizeConsideration
two-sided)
bridg:SampleSizeConsideration
based on a standard deviation of 6.5. Furthermore
bridg:SampleSizeConsideration
this sample size has 80% power to detect a 0.36 mean treatment difference in CIBIC+ (p<.05
bridg:SampleSizeConsideration
two-sided)
bridg:SampleSizeConsideration
based on a standard deviation of 0.9."
bridg:SampleSizeConsideration
InterventionalStudyProtocolVersion.interventionGroupQuantity, Arm.targetAccrualNumberRange, and StudyProtocolVersion.targetAccrualNumberRange are all related to parts of the SampleSizeConsideration that are not yet fully modeled here.
bridg:SampleSizeConsideration
urn:Statistics_v1.0:SampleSizeConsideration
bridg:ScheduledActivity
ScheduledActivity
bridg:ScheduledActivity
false
bridg:ScheduledActivity
An activity that is anticipated to occur at some time in the future and has been assigned a time or date when that activity is to be performed.
bridg:ScheduledActivity
An X-Ray scheduled for February 15 is in state "Scheduled." If John is unable to have the X-Ray on that date
bridg:ScheduledActivity
the X-Ray would either be rescheduled (remain in "Scheduled" state
bridg:ScheduledActivity
but "date" attribute would change) or moved to state "Canceled."
be participated in by actualIndicator Qualifier
bridg:ScheduledActivity
Only BiologicEntity, BiologicEntityGroup, Material, ProductGroup or Organization (via Subject or ExperimentalUnit) with actualIndicator = "true" are valid.
bridg:ScheduledActivity
urn:PSCv2.6:ScheduledStudySegment
bridg:ScheduledActivity
urn:PSCv2.6:Canceled
bridg:ScheduledActivity
urn:PSCv2.6:ScheduledActivity
bridg:ScheduledActivity
urn:PSCv2.6:Scheduled
bridg:ScheduledActivity
urn:PSCv2.6:Missed
bridg:ScheduledActivity
urn:PSCv2.6:NotApplicable
bridg:ScheduledActivity
urn:PSCv2.6:Conditional
bridg:ScheduledNotification
ScheduledNotification
bridg:ScheduledNotification
false
bridg:ScheduledNotification
An activity that represents the communication of a message to a recipient that is anticipated to occur at some time in the future and has been assigned a time or date when that activity is to be performed.
be participated in by Qualifier
bridg:ScheduledNotification
Associations from Subject (including StudySubject) are valid. Associations from ExperimentalUnit are not valid.
be received by actualIndicator Qualifier
bridg:ScheduledNotification
Only Person or Organization (via NotificationReceiver) with actualIndicator = "true" is valid.
bridg:ScheduledNotification
urn:caAERSv2.2:ScheduledNotification
bridg:ScheduledNotification
urn:caAERSv2.2:ScheduledEmailNotification
bridg:ScheduledSubstanceAdministration
ScheduledSubstanceAdministration
bridg:ScheduledSubstanceAdministration
false
bridg:ScheduledSubstanceAdministration
An activity of applying, introducing or otherwise giving medications or other substances to a subject or experimental unit that is anticipated to occur at some time in the future.
bridg:ScheduledSubstanceAdministration
Administration of methotrexate as part of chemotherapy.
activeIngredientDose Qualifier
bridg:ScheduledSubstanceAdministration
activeIngredientDose must only be used when the ScheduledSubstanceAdministration is associated to a StudyAgent that has only one active ingredient.
be participated in by Qualifier
bridg:ScheduledSubstanceAdministration
Associations from Subject (including StudySubject) are valid only for BiologicEntity, BiologicEntityGroup and Specimen, not for Product, HealthcareFacility or Organization. Associations from ExperimentalUnit are valid for BiologicEntity, BiologicEntityGroup, BiologicEntityPart and Specimen, but not for Product or ProductGroup.
bridg:Service
Service
bridg:Service
false
bridg:Service
Labor support for research.
bridg:Service
protocol management
bridg:Service
registration management
bridg:Service
data management
bridg:Service
and statistical management.
bridg:Service
urn:CTRRr3:Service
bridg:Service
urn:CTRv1.0:Service
bridg:ServiceDeliveryLocation
ServiceDeliveryLocation
bridg:ServiceDeliveryLocation
false
bridg:ServiceDeliveryLocation
A place at which services are provided by, or on behalf of, an organization.
bridg:ServiceDeliveryLocation
urn:CTRv1.0:ServiceDeliveryLocation
in R_ServiceDeliveryLocation informational
bridg:ServiceDeliveryLocation
urn:ICSRr2:ServiceDeliveryLocation
bridg:Specimen
Specimen
bridg:Specimen
false
bridg:Specimen
A substance or portion of material originally obtained from an entity for use in testing, examination, or study.
bridg:Specimen
Blood obtained by a specimen collection activity performed on a study subject.
bridg:Specimen
A few grains of cattle feed obtained from a feed sack.
bridg:Specimen
A randomly selected pill from a blister pack.
bridg:Specimen
A serum specimen that resulted from Centrifugation procedure performed on a blood specimen.
bridg:Specimen
A DNA specimen extraction from a saliva specimen.
bridg:Specimen
A Formalin-Fixed
bridg:Specimen
Paraffin-Embedded (FFPE) block that resulted from a paraffin embedding procedure performed on a formalin fixed tissue specimen.
bridg:Specimen
A pooled blood sample that resulted from a mixing procedure performed on several blood samples taken from individual animals.
bridg:Specimen
Biologic specimen
bridg:Specimen
Product specimen
bridg:Specimen
urn:CTRPv1.0:Material
bridg:Specimen
urn:CTRRr3:BiologicSpecimen
bridg:Specimen
urn:CTRv1.0:Specimen
in R_Specimen universal
bridg:Specimen
urn:ICSRr2:Product
in R_Specimen universal
bridg:Specimen
urn:ICSRr2:Specimen
bridg:Specimen
urn:LabViewer2.2:Specimen
bridg:StatisticalAnalysisPlan
StatisticalAnalysisPlan
bridg:StatisticalAnalysisPlan
false
bridg:StatisticalAnalysisPlan
A plan that encompasses all aspects of statistical activity for a study, including any statistical statements made prior to or at protocol finalization. The Statistical Analysis Plan includes a more technical and detailed elaboration than described in the protocol of the principal features of the analyses, and detailed procedures for executing the statistical analyses of the primary and secondary variables and other data.
bridg:StatisticalAnalysisPlan
The statistical analysis plan evolves during the course of the study.
bridg:StatisticalAnalysisPlan
urn:Statistics_v1.0:StatisticalAnalysisPlan
bridg:StatisticalAnalysisPlanDocumentVersion
StatisticalAnalysisPlanDocumentVersion
bridg:StatisticalAnalysisPlanDocumentVersion
false
bridg:StatisticalAnalysisPlanDocumentVersion
A representation, conceptually a document, that is created to convey the statistical analysis plan version structured content to human beings.
bridg:StatisticalAnalysisPlanDocumentVersion
urn:Statistics_v1.0:StatisticalAnalysisPlanDocumentVersion
bridg:StatisticalAnalysisPlanVersion
StatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersion
false
bridg:StatisticalAnalysisPlanVersion
A point-in-time snapshot of a statistical analysis plan.
bridg:StatisticalAnalysisPlanVersion
The statistical analysis plan evolves during the course of the study and accordingly the snapshot may address a different issue at varying levels of detail relative to the final plan.
addresses the needs of Qualifier
bridg:StatisticalAnalysisPlanVersion
The StatisticalAnalysisPlanVersion must pertain to the same StudyProtocolVersion that the StatisticalAnalysisPlan pertains to.
bridg:StatisticalAnalysisPlanVersion
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionModificationSummary
StatisticalAnalysisPlanVersionModificationSummary
bridg:StatisticalAnalysisPlanVersionModificationSummary
false
bridg:StatisticalAnalysisPlanVersionModificationSummary
Information about all changes made between the current and previous version of the statistical analysis plan.
bridg:StatisticalAnalysisPlanVersionModificationSummary
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary
bridg:StatisticalAnalysisPlanVersionStatus
StatisticalAnalysisPlanVersionStatus
bridg:StatisticalAnalysisPlanVersionStatus
false
bridg:StatisticalAnalysisPlanVersionStatus
Describes the state of the statistical analysis plan version.
bridg:StratumGroup
StratumGroup
bridg:StratumGroup
false
bridg:StratumGroup
A designation used to segregate study subjects into collections in order to balance the study for analysis. The stratum group is made up of a combination of stratification criterion answers, which ultimately is used to assign study subjects or experimental units to arms on a study.
bridg:StratumGroup
A given study may want to require even distribution of gender and age so stratum groups may be defined as: males under 18
bridg:StratumGroup
males 18 and over
bridg:StratumGroup
females under 18
bridg:StratumGroup
and females 18 and over.
bridg:StratumGroup
urn:C3PRv2.9:StratificationCriterionAnswerCombination
bridg:StratumGroup
urn:C3PRv2.9:StratumGroup
bridg:StratumGroup
urn:CTRPv1.0:StratumGroup
bridg:StratumGroup
urn:CTRPv3.8:StratumGroup
bridg:StratumGroup
urn:CTRRr3:StratumGroup
bridg:StratumGroup
urn:CTRv1.0:StratumGroup
bridg:StudyActivity
StudyActivity
bridg:StudyActivity
false
bridg:StudyActivity
The intention to use a defined activity in the design of a study.
bridg:StudyActivity
If a study's design includes the activity of taking blood pressure
bridg:StudyActivity
the DefinedActivity for blood pressure is linked to the study via this class.
bridg:StudyActivity
The number of times this activity occurs during the study and the relative timing for those occurrences is represented by PlannedActivity.
bridg:StudyActivity
urn:CTRv1.0:StudyActivity
bridg:StudyActivity
urn:HL7SD:PlannedStudy.Component2
bridg:StudyActivity
urn:caAERSv2.2:StudyTherapy
bridg:StudyAgent
StudyAgent
bridg:StudyAgent
false
bridg:StudyAgent
A product that is being used or tested as part of a study.
bridg:StudyAgent
Tamoxifen used in a breast cancer study.
bridg:StudyAgent
Fish oil used in a heart health study.
bridg:StudyAgent
Artificial knee joints used in a joint replacement study.
bridg:StudyAgent
If a study has study agents, presumably one or more of the StudyActivity will use the agent and have studyFocusedIndicator = "true".
bridg:StudyAgent
urn:CTRPv1.0:StudyProduct
bridg:StudyAgent
urn:CTRRr3:StudyAgent
bridg:StudyAgent
urn:CTRv1.0:StudyAgent
bridg:StudyAgent
urn:caAERSv2.2:StudyAgent
bridg:StudyCondition
StudyCondition
bridg:StudyCondition
false
bridg:StudyCondition
A condition that is a focus of the study.
bridg:StudyCondition
urn:C3PRv2.9:StudyDisease
bridg:StudyCondition
urn:CTRPv1.0:Conditions_or_Focus_of_Study
bridg:StudyCondition
urn:CTRPv3.8:StudyDisease
bridg:StudyCondition
urn:CTRR:Condition
bridg:StudyCondition
urn:CTRv1.0:StudyCondition
bridg:StudyCondition
urn:caAERSv2.2:AbstractStudyDisease
bridg:StudyCondition
urn:caAERSv2.2:DiseaseTerm
bridg:StudyExecution
StudyExecution
bridg:StudyExecution
false
bridg:StudyExecution
An ongoing and/or past performance of a formal investigation as specified in a study protocol.
bridg:StudyExecution
The term "protocol" is somewhat overloaded and must be qualified to provide semantic context. Therefore the term "study protocol" was chosen to disambiguate it from other protocols. The notion of a study protocol includes (but is not limited to) the design, statistical considerations, activities to test a particular hypothesis or answer a particular question that is the basis of the study, characteristics, specifications, objective(s), background, pre-study/study/post-study portions of the plan (including the design, methodology, statistical considerations, organization). The study may be of any type that involves subjects, including prevention, therapeutic, interventional or observational. Subjects involved in the study protocol may be biological entities (human, animal, specimen, tissue, organ, etc.) or products. The study protocol is related to other supporting documents, including (but not limited to) informed consent documents, case report forms (CRFs), regulatory and approval documentation, correlative studies, etc. (via the inherited association to DocumentVersionRelationship). The complete notion of the study protocol is represented in BRIDG by the classes StudyProtocol, StudyProtocolVersion, StudyProtocolDocument, StudyProtocolDocumentVersion, StudyExecution and all their associations.
- The StudyProtocol class represents the content of the study protocol which includes characteristics and plan of the study which can be distilled into or abstracted from a version of the study protocol document and can exist even before the information is put into document form.
- The StudyProtocolVersion class represents the details of the study protocol that may change over time.
- The StudyProtocolDocument class represents the document form of the study protocol and is a grouping of the various study protocol document versions.
- The StudyProtocolDocumentVersion class represents the document form of the study protocol version and is the details of the study protocol document that may change over time.
- The StudyExecution class represents the conduct of a study based on a study protocol definition which includes the scheduled and performed activities that are subject-specific as well as study-level and site-level activities.
be overseen by actualIndicator Qualifier
bridg:StudyExecution
Only Organization (via StudyOversightAuthority) with actualIndicator = "true" is valid.
use actualIndicator Qualifier
bridg:StudyExecution
Only Person or Organization (via StudyResource) with actualIndicator = "true" is valid.
bridg:StudyExecution
urn:CTRv1.0:StudyExecution
bridg:StudyExecution
urn:caAERSv2.2:Study
bridg:StudyInvestigator
StudyInvestigator
bridg:StudyInvestigator
false
bridg:StudyInvestigator
A researcher in a study who oversees multiple aspects of the study, such as concept development, protocol writing, protocol submission for IRB approval, participant recruitment, informed consent, data collection, analysis, interpretation and presentation.
be a function performed by Qualifier
bridg:StudyInvestigator
If the associated StudyProtocolVersion is an InterventionalStudyProtocolVersion then the StudyInvestigator must be a function performed by a HealthcareProvider.
bridg:StudyInvestigator
urn:C3PRv2.9:StudyInvestigator
bridg:StudyInvestigator
urn:CTRPv1.0:StudyInvestigator
bridg:StudyInvestigator
urn:CTRPv3.8:StudyInvestigator
bridg:StudyInvestigator
urn:CTRRr3:StudyInvestigator
bridg:StudyInvestigator
urn:CTRv1.0:StudyInvestigator
bridg:StudyInvestigator
urn:HL7SP:Investigator
bridg:StudyInvestigator
urn:caAERSv2.2:StudyInvestigator
bridg:StudyLegalSponsor
StudyLegalSponsor
bridg:StudyLegalSponsor
false
bridg:StudyLegalSponsor
A sponsor that initiates the investigation and is legally responsible for the study.
bridg:StudyLegalSponsor
Government Agency examples: National Cancer Institute (NCI)
bridg:StudyLegalSponsor
National Institutes of Health (NIH)
bridg:StudyLegalSponsor
National Cancer Research Institute (NCRI)
bridg:StudyLegalSponsor
Private industry examples: pharmaceutical companies
be a function performed by Exclusive Or
bridg:StudyLegalSponsor
A StudyLegalSponsor is a function performed by one and only one of the following: HealthcareProvider, Organization.
bridg:StudyLegalSponsor
urn:C3PR:StudySponsor
bridg:StudyLegalSponsor
urn:CTRR:Secondary_Sponsor
bridg:StudyLegalSponsor
urn:CTRv1.0:StudyLegalSponsor
bridg:StudyLegalSponsor
urn:HSDBv1.0:[Lead_Organization]_.Organization_Type
bridg:StudyObjective
StudyObjective
bridg:StudyObjective
false
bridg:StudyObjective
A goal that the study is aiming to achieve in terms of a scientific question to be answered by the analysis of data collected during the study.
bridg:StudyObjective
To extend the life of study participants by at least 3 years.
bridg:StudyObjective
To determine efficacy of Drug X dose 1
bridg:StudyObjective
dose 2
bridg:StudyObjective
and dose 3 as measured by the percentage of subjects experiencing headache relief.
bridg:StudyObjective
To compare overall survival in subjects with [type of cancer] who have received [prior treatment] and who are randomized to treatment with either Combination A+B or single-agent B.
bridg:StudyObjective
To select a Drug X dose for further evaluation based on comparison of the short-term antiviral activity
bridg:StudyObjective
safety
bridg:StudyObjective
and tolerability of different oral doses of Drug X in combination with Drug Y in HIV-1 infected therapy-naïve subjects.
bridg:StudyObjective
To compare the proportion of subjects developing a rash in subjects administered dermatological precautions (DP) versus subjects administered usual care precautions (UC) during 12 weeks of treatment of Drug X in [disease description] subjects.
bridg:StudyObjective
To obtain exploratory descriptive information on the relationship of tobacco use
bridg:StudyObjective
alcohol use and dietary patterns on toxicity and outcomes in males and females.
bridg:StudyObjective
StudyProtocolVersion.purposeStatement, StudyProtocolVersion.primaryPurposeTypeCode and StudyObjective may sound similar in meaning but are distinct concepts in BRIDG. StudyProtocolVersion.purposeStatement, which is an broad explanation of why a study is being conducted (e.g. determine efficacy of a drug or procedure), differs from StudyProtocolVersion.primaryPurposeTypeCode which is a classification of the purpose or intent of the study (e.g. Prevention, Treatment, Quality of Life), and that differs from StudyObjective, which describes in a specific and measurable way what the study hopes to accomplish (e.g. extend life of subjects at least 3 years, reduce frequency of symptoms).
bridg:StudyObjective
urn:CTRPv3.8:StudyObjective
bridg:StudyObjective
urn:CTRR:Objectives
bridg:StudyObjective
urn:CTRRr3:StudyObjective
bridg:StudyObjective
urn:CTRv1.0:StudyObjective
bridg:StudyOutcomeMeasure
StudyOutcomeMeasure
bridg:StudyOutcomeMeasure
false
bridg:StudyOutcomeMeasure
Specific key measurement(s) or observation(s) used to measure the effect of experimental variables on the subjects in a study, or for observational studies, to describe patterns of diseases or traits or associations with exposures, risk factors or treatment. The specific measure that receives the most emphasis in assessment that would most specifically answer the hypothesis proposed by the study design.
Mandatory Attribute Qualifier
bridg:StudyOutcomeMeasure
At least one of the following must be mandatory for StudyOutcomeMeasure: name, typeCode.
bridg:StudyOutcomeMeasure
urn:CTRPv1.0:StudyOutcomeMeasure
bridg:StudyOutcomeMeasure
urn:CTRPv3.8:StudyOutcomeMeasure
bridg:StudyOutcomeMeasure
urn:CTRRr3:StudyOutcomeMeasure
bridg:StudyOutcomeMeasure
urn:CTRv1.0:StudyOutcomeMeasure
bridg:StudyOverallStatus
StudyOverallStatus
bridg:StudyOverallStatus
false
bridg:StudyOverallStatus
Describes the comprehensive state of the study.
bridg:StudyOverallStatus
The actual overall status of a study may be derived if it is possible to roll-up the site-specific status.
bridg:StudyOverallStatus
urn:CTRPv1.0:StudyOverallStatus
bridg:StudyOverallStatus
urn:CTRPv3.8:StudyOverallStatus
bridg:StudyOverallStatus
urn:CTRRr3:StudyOverallStatus
bridg:StudyOverallStatus
urn:CTRv1.0:StudyOverallStatus
bridg:StudyOverallStatus
urn:HL7SP:Study.subjectOf1
bridg:StudyOversightAuthority
StudyOversightAuthority
bridg:StudyOversightAuthority
false
bridg:StudyOversightAuthority
An organization with monitoring, regulatory, or supervisory authority over biomedical research at the local, regional, national, or international level for a particular study.
oversee Mandatory Qualifier
bridg:StudyOversightAuthority
At least one of the following classes must be known for a StudyOversightAuthority: StudyProtocolVersion, StudyExecution.
bridg:StudyOversightAuthority
urn:CTGOV:FDA_Regulated_Intervention?
bridg:StudyOversightAuthority
urn:CTGOV:Data_Monitoring_Committee?
bridg:StudyOversightAuthority
urn:CTRPv1.0:InterventionalStudyProtocol.FDAregulatedIndicator
bridg:StudyOversightAuthority
urn:CTRPv3.8:StudyRegulatoryAuthority
bridg:StudyOversightAuthority
urn:CTRv1.0:StudyOversightAuthority
bridg:StudyOversightAuthority
urn:HSDBv1.0:[Lead_Organization]_.Organization_Type
bridg:StudyPersonnel
StudyPersonnel
bridg:StudyPersonnel
false
bridg:StudyPersonnel
A person who performs a particular role within the context of a specific study.
bridg:StudyPersonnel
Study Principal Investigator
bridg:StudyPersonnel
Coordinating Investigator
bridg:StudyPersonnel
Study Director
bridg:StudyPersonnel
Study Chair
bridg:StudyPersonnel
Public Queries
bridg:StudyPersonnel
Scientific Queries
bridg:StudyPersonnel
Scientific Leadership
be a function performed by Exclusive Or
bridg:StudyPersonnel
A StudyPersonnel might be a function performed by one and only one of the following: ResearchStaff, HealthcareProvider.
bridg:StudyPersonnel
urn:C3PRv2.9:StudyPersonnel
bridg:StudyPersonnel
urn:CTGOV:Coordinating_investigator
bridg:StudyPersonnel
urn:CTRPv3.8:StudyContact
bridg:StudyPersonnel
urn:CTRRr3:StudyColleague
bridg:StudyPersonnel
urn:CTRv1.0:StudyPersonnel
bridg:StudyProtocol
StudyProtocol
bridg:StudyProtocol
false
bridg:StudyProtocol
A discrete, structured plan (that persists over time) of a formal investigation to assess the utility, impact, pharmacological, physiological, and/or psychological effects of a particular treatment, procedure, drug, device, biologic, food product, cosmetic, care plan, or subject characteristic.
bridg:StudyProtocol
The term "protocol" is somewhat overloaded and must be qualified to provide semantic context. Therefore the term "study protocol" was chosen to disambiguate it from other protocols. The notion of a study protocol includes (but is not limited to) the design, statistical considerations, activities to test a particular hypothesis or answer a particular question that is the basis of the study, characteristics, specifications, objective(s), background, pre-study/study/post-study portions of the plan (including the design, methodology, statistical considerations, organization). The study may be of any type that involves subjects, including prevention, therapeutic, interventional or observational. Subjects involved in the study protocol may be biological entities (human, animal, specimen, tissue, organ, etc.) or products. The study protocol is related to other supporting documents, including (but not limited to) informed consent documents, case report forms (CRFs), regulatory and approval documentation, correlative studies, etc. (via the inherited association to DocumentVersionRelationship). The complete notion of the study protocol is represented in BRIDG by the classes StudyProtocol, StudyProtocolVersion, StudyProtocolDocument, StudyProtocolDocumentVersion, StudyExecution and all their associations.
- The StudyProtocol class represents the content of the study protocol which includes characteristics and plan of the study which can be distilled into or abstracted from a version of the study protocol document and can exist even before the information is put into document form.
- The StudyProtocolVersion class represents the details of the study protocol that may change over time.
- The StudyProtocolDocument class represents the document form of the study protocol and is a grouping of the various study protocol document versions.
- The StudyProtocolDocumentVersion class represents the document form of the study protocol version and is the details of the study protocol document that may change over time.
- The StudyExecution class represents the conduct of a study based on a study protocol definition which includes the scheduled and performed activities that are subject-specific as well as study-level and site-level activities.
bridg:StudyProtocol
urn:BRIDGSCC:Model_Integrity_-_Study_Versioning
bridg:StudyProtocol
urn:CTRPv3.8:StudyProtocol
bridg:StudyProtocol
urn:CTRv1.0:StudyProtocol
bridg:StudyProtocol
urn:Statistics_v1.0:StudyProtocol
bridg:StudyProtocolDocument
StudyProtocolDocument
bridg:StudyProtocolDocument
false
bridg:StudyProtocolDocument
A representation of the study protocol (that persists over time) in document form.
bridg:StudyProtocolDocument
The term "protocol" is somewhat overloaded and must be qualified to provide semantic context. Therefore the term "study protocol" was chosen to disambiguate it from other protocols. The notion of a study protocol includes (but is not limited to) the design, statistical considerations, activities to test a particular hypothesis or answer a particular question that is the basis of the study, characteristics, specifications, objective(s), background, pre-study/study/post-study portions of the plan (including the design, methodology, statistical considerations, organization). The study may be of any type that involves subjects, including prevention, therapeutic, interventional or observational. Subjects involved in the study protocol may be biological entities (human, animal, specimen, tissue, organ, etc.) or products. The study protocol is related to other supporting documents, including (but not limited to) informed consent documents, case report forms (CRFs), regulatory and approval documentation, correlative studies, etc. (via the inherited association to DocumentVersionRelationship). The complete notion of the study protocol is represented in BRIDG by the classes StudyProtocol, StudyProtocolVersion, StudyProtocolDocument, StudyProtocolDocumentVersion, StudyExecution and all their associations.
- The StudyProtocol class represents the content of the study protocol which includes characteristics and plan of the study which can be distilled into or abstracted from a version of the study protocol document and can exist even before the information is put into document form.
- The StudyProtocolVersion class represents the details of the study protocol that may change over time.
- The StudyProtocolDocument class represents the document form of the study protocol and is a grouping of the various study protocol document versions.
- The StudyProtocolDocumentVersion class represents the document form of the study protocol version and is the details of the study protocol document that may change over time.
- The StudyExecution class represents the conduct of a study based on a study protocol definition which includes the scheduled and performed activities that are subject-specific as well as study-level and site-level activities.
Document
bridg:StudyProtocolDocument
urn:CTRPv3.8:StudyProtocol.document
bridg:StudyProtocolDocument
urn:CTRv1.0:StudyProtocolDocument
bridg:StudyProtocolDocumentVersion
StudyProtocolDocumentVersion
bridg:StudyProtocolDocumentVersion
false
bridg:StudyProtocolDocumentVersion
A representation of a particular edition or snapshot of a document containing a study protocol as it exists at a particular point in time.
bridg:StudyProtocolDocumentVersion
Version 3 of a breast cancer protocol.
bridg:StudyProtocolDocumentVersion
Amendment
bridg:StudyProtocolDocumentVersion
The term "protocol" is somewhat overloaded and must be qualified to provide semantic context. Therefore the term "study protocol" was chosen to disambiguate it from other protocols. The notion of a study protocol includes (but is not limited to) the design, statistical considerations, activities to test a particular hypothesis or answer a particular question that is the basis of the study, characteristics, specifications, objective(s), background, pre-study/study/post-study portions of the plan (including the design, methodology, statistical considerations, organization). The study may be of any type that involves subjects, including prevention, therapeutic, interventional or observational. Subjects involved in the study protocol may be biological entities (human, animal, specimen, tissue, organ, etc.) or products. The study protocol is related to other supporting documents, including (but not limited to) informed consent documents, case report forms (CRFs), regulatory and approval documentation, correlative studies, etc. (via the inherited association to DocumentVersionRelationship). The complete notion of the study protocol is represented in BRIDG by the classes StudyProtocol, StudyProtocolVersion, StudyProtocolDocument, StudyProtocolDocumentVersion, StudyExecution and all their associations.
- The StudyProtocol class represents the content of the study protocol which includes characteristics and plan of the study which can be distilled into or abstracted from a version of the study protocol document and can exist even before the information is put into document form.
- The StudyProtocolVersion class represents the details of the study protocol that may change over time.
- The StudyProtocolDocument class represents the document form of the study protocol and is a grouping of the various study protocol document versions.
- The StudyProtocolDocumentVersion class represents the document form of the study protocol version and is the details of the study protocol document that may change over time.
- The StudyExecution class represents the conduct of a study based on a study protocol definition which includes the scheduled and performed activities that are subject-specific as well as study-level and site-level activities.
The term "Amendment" needs to be disambiguated since it sometimes refers to the amended version of the protocol (StudyProtocolDocumentVersion) and other times refers to the summary of changes (AmendmentChangeSummaryVersion).
bridg:StudyProtocolDocumentVersion
NOTE: BRIDG SCC acknowledges that there are two ways to represent the relationship between a study protocol and a document that is cited by the study protocol: 1) use the StudyProtocolVersion to StudyReference association; 2) use the StudyProtocolVersion > StudyProtocolDocumentVersion > DocumentVersionRelationship associations. The first is more direct and uses domain terminology, while the second is more consistent with other document-to-document associations. The SCC hopes to clarify this ambiguity in a future release when a project dealing with publications or a related area comes to harmonization.
DocumentAuthor actualIndicator Qualifier
bridg:StudyProtocolDocumentVersion
Only Person (via HealthcareProvider or ResearchStaff) with actualIndicator = "true" is valid for the DocumentAuthor of a StudyProtocolDocumentVersion.
is a version of Qualifier
bridg:StudyProtocolDocumentVersion
For a given StudyProtocolDocumentVersion, the StudyProtocol represented by the StudyProtocolDocument being versioned as the StudyProtocolDocumentVersion must be the same as the StudyProtocol whose StudyProtocolVersion is contained by the StudyProtocolDocumentVersion.
bridg:StudyProtocolDocumentVersion
urn:CTRv1.0:StudyProtocolDocumentVersion
bridg:StudyProtocolDocumentVersion
urn:caAERSv2.2:Study
bridg:StudyProtocolVersion
StudyProtocolVersion
bridg:StudyProtocolVersion
false
bridg:StudyProtocolVersion
A plan at a particular point in time for a formal investigation to assess the utility, impact, pharmacological, physiological, and/or psychological effects of a particular treatment, procedure, drug, device, biologic, food product, cosmetic, care plan, or subject characteristic.
bridg:StudyProtocolVersion
The term "protocol" is somewhat overloaded and must be qualified to provide semantic context. Therefore the term "study protocol" was chosen to disambiguate it from other protocols. The notion of a study protocol includes (but is not limited to) the design, statistical considerations, activities to test a particular hypothesis or answer a particular question that is the basis of the study, characteristics, specifications, objective(s), background, pre-study/study/post-study portions of the plan (including the design, methodology, statistical considerations, organization). The study may be of any type that involves subjects, including prevention, therapeutic, interventional or observational. Subjects involved in the study protocol may be biological entities (human, animal, specimen, tissue, organ, etc.) or products. The study protocol is related to other supporting documents, including (but not limited to) informed consent documents, case report forms (CRFs), regulatory and approval documentation, correlative studies, etc. (via the inherited association to DocumentVersionRelationship). The complete notion of the study protocol is represented in BRIDG by the classes StudyProtocol, StudyProtocolVersion, StudyProtocolDocument, StudyProtocolDocumentVersion, StudyExecution and all their associations.
- The StudyProtocol class represents the content of the study protocol which includes characteristics and plan of the study which can be distilled into or abstracted from a version of the study protocol document and can exist even before the information is put into document form.
- The StudyProtocolVersion class represents the details of the study protocol that may change over time.
- The StudyProtocolDocument class represents the document form of the study protocol and is a grouping of the various study protocol document versions.
- The StudyProtocolDocumentVersion class represents the document form of the study protocol version and is the details of the study protocol document that may change over time.
- The StudyExecution class represents the conduct of a study based on a study protocol definition which includes the scheduled and performed activities that are subject-specific as well as study-level and site-level activities.
be the responsibility of actualIndicator Qualifier
bridg:StudyProtocolVersion
Only Person or Organization (via StudyLegalSponsor) with actualIndicator = "true" is valid.
bridg:StudyProtocolVersion
urn:AE:Study
bridg:StudyProtocolVersion
urn:C3PRv2.9:Study
bridg:StudyProtocolVersion
urn:C3PRv2.9:StudyVersion
bridg:StudyProtocolVersion
urn:CTRPv1.0:StudyProtocol
bridg:StudyProtocolVersion
urn:CTRRr3:Study
bridg:StudyProtocolVersion
urn:CTRv1.0:StudyProtocolVersion
bridg:StudyProtocolVersion
urn:HL7SD:PlannedStudy
bridg:StudyProtocolVersion
urn:HL7SD:StudyCharacteristic
bridg:StudyProtocolVersion
urn:HL7SP:PlannedStudy
bridg:StudyProtocolVersion
urn:HL7SP:Study
in IndividualCaseSafetyReport
bridg:StudyProtocolVersion
urn:ICSRr2:ResearchStudy
bridg:StudyProtocolVersion
urn:LabViewer2.2:Study
bridg:StudyProtocolVersion
urn:PSCv2.6:Study
bridg:StudyProtocolVersion
urn:SDTM_IGv3.1.2:TS.DOMAIN
bridg:StudyProtocolVersion
urn:Statistics_v1.0:StudyProtocolVersion
bridg:StudyProtocolVersion
urn:caAERSv2.2:Study
bridg:StudyRecruitmentStatus
StudyRecruitmentStatus
bridg:StudyRecruitmentStatus
false
bridg:StudyRecruitmentStatus
Status of finding and enrolling appropriate study subjects (those selected on the basis of the protocol's inclusion/exclusion criteria) into a study.
bridg:StudyRecruitmentStatus
urn:CTRPv1.0:StudyRecruitmentStatus
bridg:StudyRecruitmentStatus
urn:CTRPv3.8:StudyRecruitmentStatus
bridg:StudyRecruitmentStatus
urn:CTRRr3:StudyRecruitmentStatus
bridg:StudyRecruitmentStatus
urn:CTRv1.0:StudyRecruitmentStatus
bridg:StudyRecruitmentStatus
urn:HL7SP:Study.subjectOf2
bridg:StudyReference
StudyReference
bridg:StudyReference
false
bridg:StudyReference
A citation to a publication related to the protocol's background.
bridg:StudyReference
CT.gov instruction say to provide either the unique PubMed Identifier (PMID) of an article or enter the full bibliographic citation.
bridg:StudyReference
NOTE: BRIDG SCC acknowledges that there are two ways to represent the relationship between a study protocol and a document that is cited by the study protocol: 1) use the StudyProtocolVersion to StudyReference association; 2) use the StudyProtocolVersion > StudyProtocolDocumentVersion > DocumentVersionRelationship associations. The first is more direct and uses domain terminology, while the second is more consistent with other document-to-document associations. The SCC hopes to clarify this ambiguity in a future release when a project dealing with publications or a related area comes to harmonization.
Mandatory Attribute Qualifier
bridg:StudyReference
At least one of the following must be mandatory for StudyReference: publicationIdentifier, publicationName, uniformResourceLocator, citationDescription, linkpageDescription.
bridg:StudyReference
urn:CTGOV:References
bridg:StudyReference
urn:CTRRr3:StudyReference
bridg:StudyReference
urn:CTRv1.0:StudyReference
bridg:StudyRegistry
StudyRegistry
bridg:StudyRegistry
false
bridg:StudyRegistry
An organization (typically a government agency) that administers the registration of studies.
bridg:StudyRegistry
ClinicalTrials.gov (CT.gov)
bridg:StudyRegistry
Netherlands National Trial Register (NTR)
bridg:StudyRegistry
The study registry should contain basic information about each study sufficient to inform potential subjects (and their healthcare providers) how to enroll in the study.
bridg:StudyRegistry
urn:CTOM:HealthcareSiteParticipantRole.roleCode
bridg:StudyRegistry
urn:CTRR:Registry_Protocol_Identifier_Source
bridg:StudyRegistry
urn:CTRRr3:StudyRegistry
bridg:StudyRegistry
urn:CTRv1.0:StudyRegistry
in IndividualCaseSafetyReport
bridg:StudyRegistry
urn:HL7SP:Author4
bridg:StudyResearchCoordinator
StudyResearchCoordinator
bridg:StudyResearchCoordinator
false
bridg:StudyResearchCoordinator
A person who handles the administrative responsibilities of a study on behalf of the study investigator, acts as a liaison between study site and study sponsor, and reviews all data and records before a monitor's visit.
bridg:StudyResearchCoordinator
At some sites (primarily in academic settings) Clinical Research Coordinators are called (Clinical Research Associates) CRAs.
bridg:StudyResearchCoordinator
study coordinator
bridg:StudyResearchCoordinator
research coordinator
bridg:StudyResearchCoordinator
clinical coordinator
bridg:StudyResearchCoordinator
research nurse
bridg:StudyResearchCoordinator
protocol nurse
bridg:StudyResearchCoordinator
urn:CTRRr3:StudyResearchCoordinator
bridg:StudyResource
StudyResource
bridg:StudyResource
false
bridg:StudyResource
The association between a resource and the study on which it is used.
bridg:StudyResource
urn:C3PR:StudyOrganization
bridg:StudyResource
urn:C3PRv2.9:StudyFundingSponsor
bridg:StudyResource
urn:C3PRv2.9:StudyCoordinatingCenter
bridg:StudyResource
urn:CTRPv3.8:StudyResourcing
bridg:StudyResource
urn:CTRRr3:StudyResource
bridg:StudyResource
urn:CTRv1.0:StudyResource
bridg:StudyResource
urn:caAERSv2.2:StudyFundingSponsor
bridg:StudyResource
urn:caAERSv2.2:StudyCoordinatingCenter
bridg:StudySite
StudySite
bridg:StudySite
false
bridg:StudySite
A facility in which study activities are conducted.
bridg:StudySite
The site where the study subject encounter occurs
bridg:StudySite
or the site of the Investigator.
be a function performed by Exclusive Or
bridg:StudySite
A StudySite is a function performed by one and only one of the following: HealthcareFacility or Organization (serving as a StudySite but is not a HealthcareFacility).
be a function performed by actualIndicator Qualifier
bridg:StudySite
Only Organization (via HealthcareFacility or direct association) with actualIndicator = "true" is valid.
be overseen by actualIndicator Qualifier
bridg:StudySite
Only Organization (via OversightCommittee) with actualIndicator = "true" is valid.
execute Mandatory Qualifier
bridg:StudySite
At least one of the following must be known for a StudySite: StudySiteProtocolVersionRelationship, StudyExecution.
bridg:StudySite
urn:C3PRv2.9:StudyOrganization
bridg:StudySite
urn:C3PRv2.9:StudySite
bridg:StudySite
urn:CTGOV:Facility
bridg:StudySite
urn:CTRPv1.0:StudyParticipation
bridg:StudySite
urn:CTRPv3.8:OrganizationFunctionalRole.functionCode
bridg:StudySite
urn:CTRPv3.8:StudySiteOverallStatus
bridg:StudySite
urn:CTRPv3.8:StudySite
bridg:StudySite
urn:CTRRr3:StudySite
bridg:StudySite
urn:CTRv1.0:StudySite
bridg:StudySite
urn:HL7SP:Study.performer1
bridg:StudySite
urn:HL7SP:StudySite
bridg:StudySite
urn:HL7SP:SubjectProtectionApproval
bridg:StudySite
urn:HSDBv1.0:[Lead_Organization].Organization_Type
bridg:StudySite
urn:LabViewer2.2:StudySite
bridg:StudySite
urn:PSC:StudySite
bridg:StudySite
urn:PSCv2.6:StudySite
bridg:StudySite
urn:caAERSv2.2:StudySite
bridg:StudySite
urn:caAERSv2.2:StudyOrganization
bridg:StudySiteInvestigator
StudySiteInvestigator
bridg:StudySiteInvestigator
false
bridg:StudySiteInvestigator
A researcher at a study site who oversees multiple aspects of the study at a site, including protocol submission for IRB approval, participant recruitment, informed consent, data collection, and analysis.
be a function performed by Qualifier
bridg:StudySiteInvestigator
If the associated StudyProtocolVersion is an InterventionalStudyProtocolVersion then the StudySiteInvestigator must be a function performed by a HealthcareProvider.
bridg:StudySiteInvestigator
urn:C3PRv2.9:StudyInvestigator
at the protocol location
bridg:StudySiteInvestigator
urn:CTGOV:Investigators
bridg:StudySiteInvestigator
urn:CTRPv1.0:StudySiteInvestigator
bridg:StudySiteInvestigator
urn:CTRPv3.8:StudySiteInvestigator
bridg:StudySiteInvestigator
urn:CTRv1.0:StudySiteInvestigator
bridg:StudySiteInvestigator
urn:HL7SP:Study.performer3
bridg:StudySiteOversightStatus
StudySiteOversightStatus
bridg:StudySiteOversightStatus
false
bridg:StudySiteOversightStatus
Describes the state of a study at a particular site as assigned by an oversight committee.
bridg:StudySiteOversightStatus
request not submitted; submitted
bridg:StudySiteOversightStatus
pending; submitted
bridg:StudySiteOversightStatus
approved; submitted
bridg:StudySiteOversightStatus
exempt; submitted
bridg:StudySiteOversightStatus
denied; submission not required.
be assigned by actualIndicator Qualifier
bridg:StudySiteOversightStatus
Only Organization (via OversightCommittee) with actualIndicator = "true" is valid.
bridg:StudySiteOversightStatus
urn:CTRv1.0:StudySiteOversightStatus
bridg:StudySiteOversightStatus
urn:PSCv2.6:AmendmentApproval
bridg:StudySitePersonnel
StudySitePersonnel
bridg:StudySitePersonnel
false
bridg:StudySitePersonnel
A person who performs a particular role within the context of a specific study site.
bridg:StudySitePersonnel
Study Site Investigator
bridg:StudySitePersonnel
Study Site Research Coordinator
bridg:StudySitePersonnel
roleCode and primaryIndicator are redundant attributes when roleCode = "Principal Site Investigator" and primaryIndicator ="true".
be a function performed by Exclusive Or
bridg:StudySitePersonnel
A StudySitePersonnel is a function performed by one and only one of the following: ResearchStaff, HealthcareProvider.
bridg:StudySitePersonnel
urn:C3PRv2.9:StudyPersonnel
bridg:StudySitePersonnel
urn:CTGOV:Facility_Contact
bridg:StudySitePersonnel
urn:CTRPv1.0:StudyParticipationContact
bridg:StudySitePersonnel
urn:CTRPv3.8:StudySiteContact
bridg:StudySitePersonnel
urn:CTRRr3:StudySiteContact
bridg:StudySitePersonnel
urn:CTRv1.0:StudySitePersonnel
bridg:StudySitePersonnel
urn:HL7SP:Study.performer3
bridg:StudySitePersonnel
urn:caAERSv2.2:StudyPersonnel
bridg:StudySiteProtocolVersionRelationship
StudySiteProtocolVersionRelationship
bridg:StudySiteProtocolVersionRelationship
false
bridg:StudySiteProtocolVersionRelationship
Specifies the link between a study site and a version of the study protocol used or available for use at that site.
bridg:StudySiteProtocolVersionRelationship
Even if a study site's IRB has not reviewed the study protocol version, if there is a new version for the study protocol, then there is the potential for a relationship between the site and the version. The dateRange is specified only if the version is approved for this site by the IRB and activated at the site. Retroactive approval means that the dateRange does not have to be on or after the IRB approval date.
bridg:StudySiteProtocolVersionRelationship
urn:C3PRv2.9:StudySiteStudyVersion
bridg:StudySiteProtocolVersionRelationship
urn:CTRv1.0:StudySiteProtocolVersionRelationship
bridg:StudySiteRecruitmentStatus
StudySiteRecruitmentStatus
bridg:StudySiteRecruitmentStatus
false
bridg:StudySiteRecruitmentStatus
The point-in-time expression of the progress of finding and enrolling study subjects into a study for a particular study site.
bridg:StudySiteRecruitmentStatus
urn:CTRPv3.8:StudySiteAccrualStatus
bridg:StudySiteRecruitmentStatus
urn:CTRv1.0:StudySiteRecruitmentStatus
bridg:StudySiteResearchCoordinator
StudySiteResearchCoordinator
bridg:StudySiteResearchCoordinator
false
bridg:StudySiteResearchCoordinator
A person who handles the administrative responsibilities of a study on behalf of a study site, acts as a liaison between the study site and the study investigator and/or study sponsor, and reviews all data and records before a monitor's visit.
bridg:StudySiteResearchCoordinator
At some sites (primarily in academic settings) StudySiteResearchCoordinators are called Clinical Research Coordinators or Clinical Research Associates (CRAs).
bridg:StudySiteResearchCoordinator
study coordinator
bridg:StudySiteResearchCoordinator
research coordinator
bridg:StudySiteResearchCoordinator
clinical coordinator
bridg:StudySiteResearchCoordinator
research nurse
bridg:StudySiteResearchCoordinator
protocol nurse.
bridg:StudySiteResource
StudySiteResource
bridg:StudySiteResource
false
bridg:StudySiteResource
The association between a resource and the study site on which it is used.
StudyResource
bridg:StudySiteResource
urn:CTRv1.0:StudySite.used
bridg:StudySpecificStatisticalAnalysisPlan
StudySpecificStatisticalAnalysisPlan
bridg:StudySpecificStatisticalAnalysisPlan
false
bridg:StudySpecificStatisticalAnalysisPlan
A type of statistical analysis plan that is intended to draw conclusions from only one study.
bridg:StudySpecificStatisticalAnalysisPlan
urn:Statistics_v1.0:StudySpecificStatisticalAnalysisPlan
bridg:StudySubject
StudySubject
bridg:StudySubject
false
bridg:StudySubject
A physical entity which is the primary unit of operational and/or administrative interest in a study.
bridg:StudySubject
A person who is registered in a study as a recipient of an investigational product or as a control.
bridg:StudySubject
Individuals who are being screened for studies.
bridg:StudySubject
Individuals participating in observational or other studies.
bridg:StudySubject
A pacemaker
bridg:StudySubject
a fuse that can be used in medical devices
bridg:StudySubject
a cow
bridg:StudySubject
a pen of pigs
bridg:StudySubject
or a tissue sample from a tissue bank.
bridg:StudySubject
StudySubjects within a study are all of the same type. An entity registered in a study is not part of another entity registered in the same study.
be a function performed by Not Applicable
bridg:StudySubject
Association from Organization is not valid.
bridg:StudySubject
urn:C3PRv2.9:StudySubject
StudySubject
bridg:StudySubject
urn:CTRPv3.8:Patient.
StudySubject
bridg:StudySubject
urn:CTRPv3.8:StudySite.
bridg:StudySubject
urn:CTRPv3.8:StudySubject
bridg:StudySubject
urn:CTRv1.0:StudySubject
bridg:StudySubject
urn:HL7SP:Study.subject
in IndividualCaseSafetyReport
bridg:StudySubject
urn:ICSRr2:Subject
bridg:StudySubject
urn:NCI_CRF_Standard:ParticipantIdentifier
bridg:StudySubject
urn:PSCv2.6:StudySubjectAssignment
bridg:StudySubject
urn:PSCv2.6:Subject
bridg:StudySubject
urn:SDTM_IGv3.1.2:DM.DOMAIN
bridg:StudySubjectExperienceDocumentVersion
StudySubjectExperienceDocumentVersion
bridg:StudySubjectExperienceDocumentVersion
false
bridg:StudySubjectExperienceDocumentVersion
A document capturing the actual end-to-end (or beginning to point-in-time) experience of a single study subject within the context of a particular study
be participated in by actualIndicator Qualifier
bridg:StudySubjectExperienceDocumentVersion
Only BiologicEntity, BiologicEntityGroup, Material (via StudySubject) with actualIndicator = “true” is valid.
bridg:StudySubjectExperienceDocumentVersion
urn:CTRv1.0:StudySubjectExperienceDocumentVersion
bridg:StudySubjectProtocolVersionRelationship
StudySubjectProtocolVersionRelationship
bridg:StudySubjectProtocolVersionRelationship
false
bridg:StudySubjectProtocolVersionRelationship
Specifies the link between a study subject and a version of the study protocol at a site.
bridg:StudySubjectProtocolVersionRelationship
urn:C3PRv2.9:StudySubjectStudyVersion
bridg:StudySubjectProtocolVersionRelationship
urn:CTRv1.0:StudySubjectProtocolVersionRelationship
in IndividualCaseSafetyReport
bridg:StudySubjectProtocolVersionRelationship
urn:ICSRr2:Subject12
bridg:StudySubjectProtocolVersionRelationship
urn:caAERSv2.2:StudyParticipantAssignment
bridg:Subject
Subject
bridg:Subject
false
bridg:Subject
An entity of interest, either biological or otherwise.
bridg:Subject
A human being who might be of interest because they are on a study
bridg:Subject
a sheep who might have experienced an adverse event
bridg:Subject
or a pacemaker that failed.
be a function performed by Exclusive Or
bridg:Subject
A Subject might be a function performed by one and only one of the following: BiologicEntity, BiologicEntityGroup, HealthcareFacility, Organization, Product, Specimen.
bridg:Subject
urn:AE:InvestigativeSubject
bridg:Subject
urn:C3PRv2.9:Participant
bridg:Subject
urn:CTRPv3.8:Patient
bridg:Subject
urn:CTRPv3.8:Subject
bridg:Subject
urn:CTRv1.0:Subject
bridg:Subject
urn:HCTv1.0:CDE_2705055:Lab_Results.Please_specify_the_person_for_whom_this_typing_is_being_done:
bridg:Subject
urn:HCTv1.0:CDE_2693219:Lab_Results.Who_is_being_tested_for_IDMs?
in IndividualCaseSafetyReport
bridg:Subject
urn:ICSRr2:PrimaryRole
in R_Product
bridg:Subject
urn:ICSRr2:Subject6
in IndividualCaseSafetyReport
bridg:Subject
urn:ICSRr2:Subject13
in R_Product
bridg:Subject
urn:ICSRr2:Subject5
in IndividualCaseSafetyReport
bridg:Subject
urn:ICSRr2:Subject1
in IndividualCaseSafetyReport
bridg:Subject
urn:ICSRr2:Subject14
bridg:Subject
urn:LabViewer2.2:Participant
bridg:Subject
urn:caAERSv2.2:Participant
bridg:SubjectIdentifier
SubjectIdentifier
bridg:SubjectIdentifier
false
bridg:SubjectIdentifier
The unique identification of a subject in a specified context.
bridg:SubjectIdentifier
study subject number 7 on a specific study
bridg:SubjectIdentifier
This class is a resolution of the requirement for noting the type of an identifier which is not handled by the purely technical HL7 II data type.
be assigned by Exclusive Or
bridg:SubjectIdentifier
A SubjectIdentifier is assigned by one and only one of the following: Organization, SystemOfRecord, DonorRegistry.
be assigned by actualIndicator Qualifier
bridg:SubjectIdentifier
Only Organization with actualIndicator = "true" is valid.
identifies actualIndicator Qualifier
bridg:SubjectIdentifier
Only BiologicEntity, BiologicEntityGroup, Organization (via Subject), Material (via Product, Specimen) with actualIndicator = "true" is valid.
bridg:SubjectIdentifier
urn:CTRv1.0:SubjectIdentifier
bridg:Submission
Submission
bridg:Submission
false
bridg:Submission
A compilation of the contents of one or more submission units that supports a specific regulatory purpose or decision.
bridg:Submission
A request for approval to either market a product or to allow the applicant to start testing of a proposed product.
bridg:Submission
In most cases, the compilation of the submission units is used to assess a product's quality, safety and effectiveness.
Submissions are always associated with some regulatory action (or inaction). Each submission contains their own regulatory action. Submissions (e.g., initial marketing application, supplemental marketing application) would generally be comprised of multiple submissions units.
Most typically the submission will be used to organize information based on a review clock. Receipt date from the regulatory authority is important for a submission.
groups Exclusive Or
bridg:Submission
A Submission must have one or more ReviewableUnit or SubmissionUnit but not both.
has as subject actualIndicator Qualifier
bridg:Submission
Only Product with actualIndicator = "false" is valid.
bridg:Submission
urn:CTRRr3:Submission
bridg:Submission
urn:CTRv1.0:Submission
in R_Product
bridg:Submission
urn:ICSRr2:replacementOf
bridg:Submission
urn:RPS1:Submission
bridg:SubmissionUnit
SubmissionUnit
bridg:SubmissionUnit
false
bridg:SubmissionUnit
The collection of documents provided to the regulatory authority at one time.
bridg:SubmissionUnit
A submission unit is made up of one to many document versions. Properly defined, the submission unit concept enables companies to create new submission units from any combination of new and previously submitted document versions.
In the dynamic aspects of the model, a submission unit is one message that may have a collection of many document versions. There are rules for how submission units are evaluated are described in a state diagram, and the receipt date of the submission unit "starts the clock" for the review of the contents of the submission unit.
bridg:SubmissionUnit
NOTE: Until further clarification, the BRIDG SCC believes the IND/IDE regulatory application serial number is the number assigned by the applicant/sponsor to a document that is either a supplement or an amendment to the original submission unit and is represented using DocumentIdentifier.identifer.
be grouped into Exclusive Or
bridg:SubmissionUnit
A SubmissionUnit might be grouped into one and only one of the following: Submission, ReviewableUnit.
bridg:SubmissionUnit
urn:CTRRr3:SubmissionUnit
bridg:SubmissionUnit
urn:CTRv1.0:SubmissionUnit
bridg:SubmissionUnit
urn:RPS1:SubmissionUnit
bridg:SubstanceExtractionAdministrationRelationship
SubstanceExtractionAdministrationRelationship
bridg:SubstanceExtractionAdministrationRelationship
false
bridg:SubstanceExtractionAdministrationRelationship
Specifies the link between an extraction (performed substance extraction) of a biologic product and the administration (performed substance administration) of that biologic product.
bridg:SubstanceExtractionAdministrationRelationship
urn:HCTv1.0:CDE_2761889:DONOR'.Autologous_HSCT?
bridg:SupplementalStatisticalAnalysisPlanVersion
SupplementalStatisticalAnalysisPlanVersion
bridg:SupplementalStatisticalAnalysisPlanVersion
false
bridg:SupplementalStatisticalAnalysisPlanVersion
A type of statistical analysis plan version that provides specification for additional analyses not included as part of the principal statistical analysis plan version.
bridg:SupplementalStatisticalAnalysisPlanVersion
Additional analyses during clinical study report preparation
bridg:SupplementalStatisticalAnalysisPlanVersion
Response to regulatory request
bridg:SupplementalStatisticalAnalysisPlanVersion
Hypothesis generation
bridg:SupplementalStatisticalAnalysisPlanVersion
Pre-specified PK analysis plan
bridg:SupplementalStatisticalAnalysisPlanVersion
Analysis plan for sub-study or study addendum
bridg:SupplementalStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:SupplementalStatisticalAnalysisPlanVersion
bridg:SystemOfRecord
SystemOfRecord
bridg:SystemOfRecord
false
bridg:SystemOfRecord
The system that assigned the identifier.
bridg:SystemOfRecord
This concept will be re-visited again in the next release. It may be an implementation-oriented concept.
bridg:SystemOfRecord
urn:CTRv1.0:SystemOfRecord
bridg:SystemOfRecord
urn:caAERSv2.2:SystemAssignedIdentifier
bridg:TargetAnatomicSite
TargetAnatomicSite
bridg:TargetAnatomicSite
false
bridg:TargetAnatomicSite
An anatomic location that is the focus of an observation result.
bridg:TargetAnatomicSite
brainstem
bridg:TargetAnatomicSite
spinal cord for a lesion
bridg:TargetAnatomicSite
arm for skin rash
bridg:TreatingSite
TreatingSite
bridg:TreatingSite
false
bridg:TreatingSite
Any healthcare facility where care is provided as part of a cooperative group organizational network.
bridg:TreatingSite
A cancer center that is part of the North Central Cancer Treatment Group (NCCTG).
bridg:TreatingSite
There are two ways a TreatingSite can be associated to a CooperativeGroup: either directly or through a CooperativeGroupMember.
be a member of Exclusive Or
bridg:TreatingSite
A TreatingSite might be associated to one and only one of the following: CooperativeGroupMember, CooperativeGroup.
bridg:TreatingSite
urn:C3PR:StudyCoordinatingCenter
bridg:TreatingSite
urn:CTOM:HealthcareSiteParticipantRole.roleCode
bridg:TreatingSite
urn:CoopGrp:TreatingSite
bridg:Activity.comment
comment
bridg:Activity.comment
false
bridg:Activity.comment
Additional description of the activity.
bridg:Activity.comment
Guidance on how to perform the observation. (for DefinedObservation.comment)
bridg:Activity.comment
urn:CTRPv1.0:SubstanceAdministration.comment
bridg:Activity.comment
urn:CTRPv1.0:PlannedObservation.comment
bridg:Activity.comment
urn:CTRPv1.0:Activity.comment
bridg:Activity.comment
urn:CTRPv1.0:PlannedEligibilityCriterion.comment
bridg:Activity.comment
urn:CTRPv1.0:PlannedActivity.comment
bridg:Activity.comment
urn:CTRv1.0:Activity.comment
in IndividualCaseSafetyReport
bridg:Activity.comment
urn:ICSRr2:CausalityAssessment.text
bridg:Activity.comment
urn:Lab:LabTest.comments
bridg:Activity.comment
urn:Lab:Specimen.commentsFromInvestigator
bridg:Activity.comment
urn:Lab:Specimen.commentsFromLaboratory
bridg:Activity.comment
urn:LabViewer2.2:LaboratoryTest.comment
bridg:Activity.comment
urn:LabViewer2.2:Specimen.commentFromLaboratory
bridg:Activity.comment
urn:PSC:ScheduledEvent.notes
bridg:Activity.comment
urn:PSCv2.6:ScheduledActivity.notes
bridg:Activity.comment
urn:caAERSv2.2:CourseAgent.comments
bridg:Activity.comment
urn:caAERSv2.2:ReportReviewComment
bridg:Activity.comment
urn:caAERSv2.2:TreatmentAssignment.comments
bridg:Activity.identifier
identifier
bridg:Activity.identifier
false
bridg:Activity.identifier
A unique symbol that establishes identity of an activity.
bridg:Activity.identifier
12345 is the identifier for a substance administration
bridg:Activity.identifier
urn:CTRPv1.0:Activity.identifier
bridg:Activity.identifier
urn:CTRPv1.0:SubstanceAdministration.identifier
bridg:Activity.identifier
urn:CTRPv1.0:PlannedActivity.identifier
bridg:Activity.identifier
urn:CTRPv1.0:PlannedEligibilityCriterion.identifier
bridg:Activity.identifier
urn:CTRPv1.0:PlannedObservation.identifier
bridg:Activity.identifier
urn:CTRPv3.8:Activity.identifier
bridg:Activity.identifier
urn:CTRRr3:Activity.identifier
bridg:Activity.identifier
urn:CTRv1.0:Activity.identifier
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol//plannedStudy/precondition/eligibilityCriterion.id
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Observation.id
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.id
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Procedure.id
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Encounter.id
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Act.id
bridg:Activity.identifier
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component4/timePointEventDefinition.id
in R_Product
bridg:Activity.identifier
urn:ICSRr2:ProductEvent.id
in R_Product
bridg:Activity.identifier
urn:ICSRr2:TransportationEvent.id
in IndividualCaseSafetyReport
bridg:Activity.identifier
urn:ICSRr2:AdverseEffectReference.id
bridg:Activity.identifier
urn:Lab:Activity.identifier
bridg:Activity.identifier
urn:LabViewer2.2:LaboratoryTestIdentifier
bridg:Activity.identifier
urn:LabViewer2.2:Activity.identifier
bridg:Activity.identifier
urn:LabViewer2.2:SpecimenCollection.identifier
bridg:Activity.identifier
urn:SDTM_IGv3.1.2:DS.DSREFID
bridg:Activity.reasonCode
reasonCode
bridg:Activity.reasonCode
false
bridg:Activity.reasonCode
A coded value specifying the motivation, cause, or rationale of an activity.
bridg:Activity.reasonCode
routine requirement
bridg:Activity.reasonCode
drug reaction
bridg:Activity.reasonCode
infectious disease reporting requirement
bridg:Activity.reasonCode
on patient request
bridg:Activity.reasonCode
The key difference in how this attribute is used across the Activity subclasses is temporal and the attribute has essentially the same meaning wherever it is used. The most likely uses of reasonCode are with PlannedActivities, where it identifies why an activity should be done as part of the study plan, and with PerformedActivities, where it identifies why an activity was done. While it's possible for a DefinedActivity to have a reason, BRIDG has no use cases for the use of this attribute in a DefinedActivity, though some may come to harmonization in the future. Nor is it likely, based on existing use cases, to be used much, if at all, for ScheduledActivities.
bridg:Activity.reasonCode
urn:AE:Indication
bridg:Activity.reasonCode
urn:AE:ProductInvestigation.reasonCode
bridg:Activity.reasonCode
urn:C3PRv2.9:StudySubject.backDatedReasonCode
bridg:Activity.reasonCode
urn:C3PRv2.9:ScheduledEpoch.disapprovalReasonText
bridg:Activity.reasonCode
urn:C3PRv2.9:ScheduledEpoch.eligibilityWaiverReasonText
bridg:Activity.reasonCode
urn:C3PRv2.9:ScheduledArm.eligibilityWaiverReasonText
bridg:Activity.reasonCode
urn:C3PRv2.9:ScheduledEpoch.offEpochReasonText
bridg:Activity.reasonCode
urn:CDASHv1.1:CM.CMINDC
bridg:Activity.reasonCode
urn:CTOM:SpecimenAcquisition.reasonCode
bridg:Activity.reasonCode
urn:CTOM:Procedure.reasonCode
bridg:Activity.reasonCode
urn:CTOM:SubstanceAdministration.reasonCode
bridg:Activity.reasonCode
urn:CTOM:Radiation.reasonCode
bridg:Activity.reasonCode
urn:CTOM:Activity.reasonCode
bridg:Activity.reasonCode
urn:CTOM:Surgery.reasonCode
bridg:Activity.reasonCode
urn:CTOM:FemaleReproductiveCharacteristic.menopauseReasonCode
bridg:Activity.reasonCode
urn:CTOM:Imaging.reasonCode
bridg:Activity.reasonCode
urn:CTOM:FemaleReproductiveCharacteristic.menopauseReasonOtherText
bridg:Activity.reasonCode
urn:CTRPv1.0:SubstanceAdministration.reasonCode
bridg:Activity.reasonCode
urn:CTRPv1.0:PlannedEligibilityCriterion.reasonCode
bridg:Activity.reasonCode
urn:CTRPv1.0:PlannedActivity.reasonCode
bridg:Activity.reasonCode
urn:CTRPv1.0:PlannedObservation.reasonCode
bridg:Activity.reasonCode
urn:CTRPv1.0:Activity.reasonCode
bridg:Activity.reasonCode
urn:CTRPv3.8:PerformedSubjectMilestone.reasonCode
bridg:Activity.reasonCode
urn:CTRv1.0:Activity.reasonCode
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2957528:Therapies.Specify_the_reason_for_the_current_HSCT:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_3181140:Therapies.Therapeutic_procedure_administered_begin_reason:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2680966:Therapies.DCI_indication_other:_specify
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2744499:Therapies.Purpose_of_therapy:
s for the supplemental intravenous immunoglobulin therapy:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2775979:Therapies.Specify_the_indication
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2775984:Therapies.Specify_the_other_indication_type_for_the_supplemental_intravenous_immunoglobulin_therapy:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2771502:Therapies.Specify_the_other_indication_for_the_subsequent_HSCT:
bridg:Activity.reasonCode
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Specificity__2_of_product
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2691344:Therapies.Specify_the_indication_for_the_other_alternative_HCT:
HCT?
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2691434:Therapies.What_was_the_indication_for_the_alternative_hematopoietic_cell_transplantation
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2680962:Therapies.Indication_for_DCI
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2861356:Therapies.Indication_for_therapy:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2957419:Therapies.What_was_the_reason_for_the_current_HSCT:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2737040:Preparative_Regimen.What_was_the_reason_for_the_reduced_intensity/_non-myeloablative_preparative_regimen?
bridg:Activity.reasonCode
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Specificity__1_of_product
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2771490:Therapies.What_was_the_indication_for_the_subsequent_HSCT?
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2861364:Therapies.If_code__4__other_for_indication_of_therapy__specify:
NST / RIC preparative regimen:
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2737050:Therapies.Specify_the_other_reason_for_the_non-myeloablative_/_reduced_intensity
bridg:Activity.reasonCode
urn:HCTv1.0:CDE_2775815:Therapies.What_was_the_reason_hematopoietic__lymphoid_growth_factors_or_cytokines_were_administered?
in IndividualCaseSafetyReport
bridg:Activity.reasonCode
urn:ICSRr2:CausalityAssessment.reasonCode
bridg:Activity.reasonCode
urn:Lab:Activity.reason
bridg:Activity.reasonCode
urn:LabViewer2.2:Activity.reason
bridg:Activity.reasonCode
urn:LabViewer2.2:SpecimenCollection.reason
bridg:Activity.reasonCode
urn:NCI_CRF_Standard:CDE_2003870v4.0:_Concomitant_Agent_Concomitant_Intervention_or_Procedure_Reason
bridg:Activity.reasonCode
urn:PSC:Occurred.reason
bridg:Activity.reasonCode
urn:PSC:ScheduledEventState.reason
bridg:Activity.reasonCode
urn:PSC:Scheduled.reason
bridg:Activity.reasonCode
urn:SDTM_IGv3.1.1:CM.CMINDC
bridg:Activity.reasonCode
urn:SDTM_IGv3.1.1:DS.DSTERM
bridg:Activity.reasonCode
urn:SDTM_IGv3.1.2:CM.CMINDC
bridg:Activity.reasonCode
urn:TDM:ContactActivityPurpose.purposeType
bridg:AdverseEvent.categoryCode
categoryCode
bridg:AdverseEvent.categoryCode
false
bridg:AdverseEvent.categoryCode
A coded value specifying a classification of the adverse event.
bridg:AdverseEvent.categoryCode
bleeding
bridg:AdverseEvent.categoryCode
hypoglycemia
bridg:AdverseEvent.categoryCode
Theoretically speaking, the category should be derivable from the subcategory, however if there may only be a category and not a subcategory, then both attributes must be present in the model.
bridg:AdverseEvent.categoryCode
urn:CTRv1.0:AdverseEvent.categoryCode
bridg:AdverseEvent.categoryCode
urn:SDTM_IGv3.1.1:AE.AECAT
bridg:AdverseEvent.categoryCode
urn:SDTM_IGv3.1.2:AE.AECAT
bridg:AdverseEvent.endRelativeToReferenceCode
endRelativeToReferenceCode
bridg:AdverseEvent.endRelativeToReferenceCode
true
bridg:AdverseEvent.endRelativeToReferenceCode
A coded value specifying the end of the adverse event with respect to the sponsor-defined reference period.
bridg:AdverseEvent.endRelativeToReferenceCode
before
bridg:AdverseEvent.endRelativeToReferenceCode
during
bridg:AdverseEvent.endRelativeToReferenceCode
during/after
bridg:AdverseEvent.endRelativeToReferenceCode
after
bridg:AdverseEvent.endRelativeToReferenceCode
Sponsors should define the reference period in the study metadata. This may be populated when a start date is not collected.
Derived from AdverseEvent.occurrenceDateRange.IVL<TS.DATETIME>.high.TS.DATETIME.uncertainRange.IVL<TS.DATETIME>.high = PerformedStudySubjectMilestone.studyReferenceDateRange then "BEFORE"
AND
AdverseEvent.occurenceDateRange.IVL<TS.DATETIME>.low.TS.DATETIME.uncertainRange.IVL<TS.DATETIME>.low = PerformedStudySubjectMilestone.studyReferenceDateRange then "AFTER"
bridg:AdverseEvent.endRelativeToReferenceCode
urn:PSCv2.6:AdverseEvent.description
bridg:AdverseEvent.endRelativeToReferenceCode
urn:SDTM_IGv3.1.1:AE.ENRF
bridg:AdverseEvent.endRelativeToReferenceCode
urn:SDTM_IGv3.1.2:AE.ENRF
bridg:AdverseEvent.expectedIndicator
expectedIndicator
bridg:AdverseEvent.expectedIndicator
false
bridg:AdverseEvent.expectedIndicator
Specifies whether the specificity (nature), frequency, or severity of an adverse event is consistent with the applicable study documentation (e.g., investigator's brochure, protocol document, or consent document) or product labeling (package insert).
bridg:AdverseEvent.expectedIndicator
urn:AE:AdverseEvent.expectedIndicator
bridg:AdverseEvent.expectedIndicator
urn:CTRPv1.0:AdverseEvent.expectedIndicator
bridg:AdverseEvent.expectedIndicator
urn:CTRv1.0:AdverseEvent.expectedIndicator
bridg:AdverseEvent.expectedIndicator
urn:NCI_CRF_Standard:CDE_2183619v1.0:_Adverse_Event_Expected_Indicator
bridg:AdverseEvent.expectedIndicator
urn:caAERSv2.2:AdverseEvent.expected
bridg:AdverseEvent.gradeCode
gradeCode
bridg:AdverseEvent.gradeCode
true
bridg:AdverseEvent.gradeCode
A coded value specifying the level of injury suffered by the subject or study subject for whom the event is reported.
bridg:AdverseEvent.gradeCode
The gradeCode could be 3 if the CTCAE coding system is being used.
bridg:AdverseEvent.gradeCode
Derived from PerformedClinicalInterpretation.value(ANY=>CD).code WHERE PerformedObservationResult > PerformedObservation > DefinedObservation.nameCode = "grade assessment"
bridg:AdverseEvent.gradeCode
urn:AE:AdverseEvent.gradeOrSeverity
bridg:AdverseEvent.gradeCode
urn:CDASHv1.1:AE.AETOXGR
bridg:AdverseEvent.gradeCode
urn:CTOM:AdverseEvent.ctcGradeCodeSystem
bridg:AdverseEvent.gradeCode
urn:CTOM:AdverseEvent.ctcGradeCode
bridg:AdverseEvent.gradeCode
urn:CTRv1.0:AdverseEvent.gradeCode
bridg:AdverseEvent.gradeCode
urn:NCI_CRF_Standard:CDE_2944515v1.0:_Adverse_Event_Severity_Grade
bridg:AdverseEvent.gradeCode
urn:NCI_CRF_Standard:CDE_2201188v1.0:_Common_Toxicity_Criteria_Adverse_Event_Reporting_Grade
bridg:AdverseEvent.gradeCode
urn:PSCv2.6:AdverseEvent.description
bridg:AdverseEvent.gradeCode
urn:SDTM_IGv3.1.1:AE.AETOXGR
bridg:AdverseEvent.gradeCode
urn:SDTM_IGv3.1.2:AE.AETOXGR
bridg:AdverseEvent.gradeCode
urn:caAERSv2.2:AdverseEvent.grade
bridg:AdverseEvent.highlightedIndicator
highlightedIndicator
bridg:AdverseEvent.highlightedIndicator
false
bridg:AdverseEvent.highlightedIndicator
Specifies whether the adverse event or reaction term is a major concern or reason for reporting the adverse event.
bridg:AdverseEvent.highlightedIndicator
urn:AE:AdverseEvent.highlightedIndicator
bridg:AdverseEvent.highlightedIndicator
urn:CTRv1.0:AdverseEvent.highlightedIndicator
bridg:AdverseEvent.hospitalizationRequiredIndicator
hospitalizationRequiredIndicator
bridg:AdverseEvent.hospitalizationRequiredIndicator
false
bridg:AdverseEvent.hospitalizationRequiredIndicator
Specifies whether the subject or study subject requires hospitalization or prolongation of existing hospitalization as a result of the adverse event.
bridg:AdverseEvent.hospitalizationRequiredIndicator
urn:AE:AdverseEvent.hospitalizationRequiredIndicator
bridg:AdverseEvent.hospitalizationRequiredIndicator
urn:CTRv1.0:AdverseEvent.hospitalizationRequiredIndicator
bridg:AdverseEvent.hospitalizationRequiredIndicator
urn:NCI_CRF_Standard:CDE_2552398v1.0:_Patient_Toxicity_Hospitalization_Indicator
bridg:AdverseEvent.hospitalizationRequiredIndicator
urn:SDTM_IGv3.1.1:AE.AESHOSP
bridg:AdverseEvent.hospitalizationRequiredIndicator
urn:caAERSv2.2:AdverseEvent.hospitalization
bridg:AdverseEvent.locationDescription
locationDescription
bridg:AdverseEvent.locationDescription
false
bridg:AdverseEvent.locationDescription
The textual representation of the physical location of the subject or study subject when the adverse event began.
bridg:AdverseEvent.locationDescription
urn:CTRv1.0:AdverseEvent.locationDescription
bridg:AdverseEvent.locationDescription
urn:caAERSv2.2:AdverseEvent.eventLocation
bridg:AdverseEvent.occurrenceDateRange
occurrenceDateRange
bridg:AdverseEvent.occurrenceDateRange
false
bridg:AdverseEvent.occurrenceDateRange
The date and time span in which the adverse event began and ended.
bridg:AdverseEvent.occurrenceDateRange
onset date
bridg:AdverseEvent.occurrenceDateRange
resolution date
bridg:AdverseEvent.occurrenceDateRange
duration
bridg:AdverseEvent.occurrenceDateRange
These may be partial dates or durations (duration is the width property of the IVL<TS> data type).
bridg:AdverseEvent.occurrenceDateRange
urn:AE:AdverseEvent.onsetDate
bridg:AdverseEvent.occurrenceDateRange
urn:AE:AdverseEvent.resolutionDate
bridg:AdverseEvent.occurrenceDateRange
urn:CDASHv1.1:AE.AEENDAT
bridg:AdverseEvent.occurrenceDateRange
urn:CDASHv1.1:AE.AEENTIM
bridg:AdverseEvent.occurrenceDateRange
urn:CDASHv1.1:AE.AESTDAT
bridg:AdverseEvent.occurrenceDateRange
urn:CDASHv1.1:AE.AESTTIM
bridg:AdverseEvent.occurrenceDateRange
urn:CTOM:AdverseEvent.resolvedDate
bridg:AdverseEvent.occurrenceDateRange
urn:CTOM:AdverseEvent.onsetDate
bridg:AdverseEvent.occurrenceDateRange
urn:NCI_CRF_Standard:CDE_2189843v1.0:_Adverse_Event_Resolved_Alpha_DVG_Date
bridg:AdverseEvent.occurrenceDateRange
urn:NCI_CRF_Standard:CDE_2744993v1.0:_Adverse_Event_Onset_Date
bridg:AdverseEvent.occurrenceDateRange
urn:NCI_CRF_Standard:CDE_2585234v1.0:_Adverse_Event_Onset_Time
bridg:AdverseEvent.occurrenceDateRange
urn:NCI_CRF_Standard:CDE_2746301v1.0:_Adverse_Event_Resolution_Time
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.1:AE.AEENDTC
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.1:AE.DUR
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.1:AE.AESTDTC
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.2:AE.AEDUR
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.2:AE.AEENDTC
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.2:AE.AESTDTC
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.2:AE.AEENRF
bridg:AdverseEvent.occurrenceDateRange
urn:SDTM_IGv3.1.2:AE.AEENRTPT
bridg:AdverseEvent.occurrenceDateRange
urn:caAERSv2.2:AdverseEvent.startDate
bridg:AdverseEvent.occurrenceDateRange
urn:caAERSv2.2:AdverseEvent.endDate
bridg:AdverseEvent.occurrenceDateRange
urn:caAERSv2.2:AdverseEvent.eventApproximateTime
bridg:AdverseEvent.occurrencePatternCode
occurrencePatternCode
bridg:AdverseEvent.occurrencePatternCode
false
bridg:AdverseEvent.occurrencePatternCode
A coded value specifying the time recurrence by which an adverse event occurs.
bridg:AdverseEvent.occurrencePatternCode
intermittent
bridg:AdverseEvent.occurrencePatternCode
continuous
bridg:AdverseEvent.occurrencePatternCode
single event
bridg:AdverseEvent.occurrencePatternCode
urn:AE:AdverseEvent.patternCode
bridg:AdverseEvent.occurrencePatternCode
urn:CTOM:AdverseEvent.conditionPatternCode
bridg:AdverseEvent.occurrencePatternCode
urn:CTRv1.0:AdverseEvent.occurrencePatternCode
bridg:AdverseEvent.occurrencePatternCode
urn:NCI_CRF_Standard:CDE_2008418v1.0:_Adverse_Event_Condition_Pattern
bridg:AdverseEvent.occurrencePatternCode
urn:PSCv2.6:AdverseEvent.description
bridg:AdverseEvent.occurrencePatternCode
urn:SDTM_IGv3.1.1:AE.AEPATT
bridg:AdverseEvent.occurrencePatternCode
urn:SDTM_IGv3.1.2:AE.AEPATT
bridg:AdverseEvent.occurrencePatternCode
urn:caAERSv2.2:AdverseEventResponseDescription.eventReappear
bridg:AdverseEvent.postReportUpdateDate
postReportUpdateDate
bridg:AdverseEvent.postReportUpdateDate
false
bridg:AdverseEvent.postReportUpdateDate
The date (and time) on which the adverse event was updated after it had been submitted.
bridg:AdverseEvent.postReportUpdateDate
urn:CTRv1.0:AdverseEvent.postReportUpdateDate
bridg:AdverseEvent.postReportUpdateDate
urn:caAERSv2.2:AdverseEvent.postSubmissionUpdatedDate
bridg:AdverseEvent.severityCode
severityCode
bridg:AdverseEvent.severityCode
true
bridg:AdverseEvent.severityCode
A coded value specifying the intensity of the event.
bridg:AdverseEvent.severityCode
Moderate could be used to describe acne.
bridg:AdverseEvent.severityCode
Derived from the maximum severity observed during the course of the AdverseEvent:
PerformedClinicalInterpretation.value(ANY=>CD).code WHERE PerformedClinicalInterpretation > PerformedObservation > DefinedObservation.nameCode = "assess severity" AND PerformedObservation > AssessedResultRelationship > AdverseEvent.
bridg:AdverseEvent.severityCode
urn:AE:AdverseEvent.gradeOrSeverity
bridg:AdverseEvent.severityCode
urn:CDASHv1.1:AE.AESEV
bridg:AdverseEvent.severityCode
urn:CTRv1.0:AdverseEvent.severityCode
bridg:AdverseEvent.severityCode
urn:PSCv2.6:AdverseEvent.description
bridg:AdverseEvent.severityCode
urn:SDTM_IGv3.1.1:AE.AESEV
bridg:AdverseEvent.severityCode
urn:SDTM_IGv3.1.2:AE.AESEV
bridg:AdverseEvent.subcategoryCode
subcategoryCode
bridg:AdverseEvent.subcategoryCode
false
bridg:AdverseEvent.subcategoryCode
A coded value specifying a subdivision within a larger category of an adverse event.
bridg:AdverseEvent.subcategoryCode
neurologic
bridg:AdverseEvent.subcategoryCode
Theoretically speaking, the category should be derivable from the subcategory, however if there may only be a category and not a subcategory, then both attributes must be present in the model.
bridg:AdverseEvent.subcategoryCode
urn:CTRv1.0:AdverseEvent.subcategoryCode
bridg:AdverseEvent.subcategoryCode
urn:SDTM_IGv3.1.1:AE.AESCAT
bridg:AdverseEvent.subcategoryCode
urn:SDTM_IGv3.1.2:AE.AESCAT
bridg:AdverseEvent.summary
summary
bridg:AdverseEvent.summary
false
bridg:AdverseEvent.summary
A description of the adverse event and the treatment of the event.
bridg:AdverseEvent.summary
urn:CTRv1.0:AdverseEvent.summary
bridg:AdverseEvent.summary
urn:caAERSv2.2:AdverseEventResponseDescription.eventDescription
bridg:AdverseEvent.treatmentEmergentIndicator
treatmentEmergentIndicator
bridg:AdverseEvent.treatmentEmergentIndicator
false
bridg:AdverseEvent.treatmentEmergentIndicator
Specifies whether the adverse event is something that first arose or become more severe during the studied treatment.
bridg:AdverseEvent.treatmentEmergentIndicator
This may be derivable if a complete study subject history exists and it can be known with certainty whether (and with what severity) a condition may have pre-existed. However, this information is not always available and therefore the attribute has not been marked as derived.
bridg:AdverseEvent.treatmentEmergentIndicator
urn:CTRv1.0:AdverseEvent.treatmentEmergentIndicator
bridg:AdverseEvent.unexpectedReasonCode
unexpectedReasonCode
bridg:AdverseEvent.unexpectedReasonCode
false
bridg:AdverseEvent.unexpectedReasonCode
A coded value specifying why an adverse event (experience or reaction) is considered unanticipated.
bridg:AdverseEvent.unexpectedReasonCode
severity
bridg:AdverseEvent.unexpectedReasonCode
frequency
bridg:AdverseEvent.unexpectedReasonCode
or specificity from what has been previously documented
bridg:AdverseEvent.unexpectedReasonCode
urn:AE:AdverseEvent.unexpectedReason
bridg:AdverseEvent.unexpectedReasonCode
urn:CTRv1.0:AdverseEvent.unexpectedReasonCode
bridg:AdverseEvent.unexpectedReasonCode
urn:PSCv2.6:AdverseEvent.description
bridg:AdverseEventSeriousness.code
code
bridg:AdverseEventSeriousness.code
false
bridg:AdverseEventSeriousness.code
A coded value specifying the degree or extent of the consequence suffered by the subject or study subject.
bridg:AdverseEventSeriousness.code
resulted in death
bridg:AdverseEventSeriousness.code
required hospitalization
bridg:AdverseEventSeriousness.code
was life threatening
bridg:AdverseEventSeriousness.code
Results in Death; Is life-threatening; Requires inpatient hospitalization or prolongation of existing hospitalization; Results in persistent or significant disability/incapacity; Is a congenital anomaly/birth defect; In the medical judgment of the treating physician and/or investigator
bridg:AdverseEventSeriousness.code
it may jeopardize the participant or require intervention to prevent one of these outcomes; Other
bridg:AdverseEventSeriousness.code
specify; Meets criteria per protocol but does not meet other criterion (NCI CRF Standard)
bridg:AdverseEventSeriousness.code
urn:AE:AdverseEvent.seriousnessCode
bridg:AdverseEventSeriousness.code
urn:CDASHv1.1:AE.AESLIFE
bridg:AdverseEventSeriousness.code
urn:CTOM:AdverseEvent.seriousReasonCode
bridg:AdverseEventSeriousness.code
urn:CTRv1.0:AdverseEventSeriousness.code
bridg:AdverseEventSeriousness.code
urn:NCI_CRF_Standard:CDE_2179679v3.0:_Serious_Adverse_Event_Description_Reason_Text
bridg:AdverseEventSeriousness.code
urn:SDTM_IGv3.1.1:AE.AESHOSP
bridg:AdverseEventSeriousness.code
urn:SDTM_IGv3.1.1:AE.AESER
bridg:AdverseEventSeriousness.code
urn:SDTM_IGv3.1.2:AE.AESLIFE
bridg:AdverseEventSeriousness.code
urn:caAERSv2.2:Outcome.type
bridg:AdverseEventSeriousness.code
urn:caAERSv2.2:Outcome.other
bridg:AdverseEventSeriousness.date
date
bridg:AdverseEventSeriousness.date
false
bridg:AdverseEventSeriousness.date
The date (and time) on which the seriousness code was assigned to the adverse event.
bridg:AdverseEventSeriousness.date
urn:CTRv1.0:AdverseEventSeriousness.date
bridg:AdverseEventSeriousness.date
urn:caAERSv2.2:Outcome.date
bridg:Animal.breedCode
breedCode
bridg:Animal.breedCode
false
bridg:Animal.breedCode
A coded value specifying a group of animals presumably related by descent from common ancestors and are visibly similar in most characteristics.
bridg:Animal.breedCode
Holstein
bridg:Animal.breedCode
Angora
bridg:Animal.breedCode
Himalayan cat
bridg:Animal.breedCode
Labrador Retriever
bridg:Animal.breedCode
urn:AE:Animal.breed
bridg:Animal.breedCode
urn:CTRv1.0:Animal.breedCode
bridg:Animal.description
description
bridg:Animal.description
false
bridg:Animal.description
A textual or media-based representation of the animal.
bridg:Animal.description
paragraph description
bridg:Animal.description
digital photo
bridg:Animal.description
audio track
bridg:Animal.description
urn:CTRv1.0:Animal.description
bridg:Animal.description
urn:HL7SP:Animal.desc
in IndividualCaseSafetyReport
bridg:Animal.description
urn:ICSRr2:Animal.desc
bridg:Animal.reproductiveOrgansPresentIndicator
reproductiveOrgansPresentIndicator
bridg:Animal.reproductiveOrgansPresentIndicator
false
bridg:Animal.reproductiveOrgansPresentIndicator
Specifies whether the anatomical parts of the body involved in reproduction are present.
bridg:Animal.reproductiveOrgansPresentIndicator
If the animal has been spayed or neutered
bridg:Animal.reproductiveOrgansPresentIndicator
reproductiveOrgansPresentIndicator = "false".
bridg:Animal.reproductiveOrgansPresentIndicator
urn:AE:Organism.genderStatus
bridg:Animal.reproductiveOrgansPresentIndicator
urn:CTRv1.0:Animal.reproductiveOrgansPresentIndicator
bridg:Animal.reproductiveOrgansPresentIndicator
urn:HL7SP:Animal.genderStatusIndicator
in IndividualCaseSafetyReport
bridg:Animal.reproductiveOrgansPresentIndicator
urn:ICSRr2:Animal.genderStatusCode
bridg:Animal.speciesCode
speciesCode
bridg:Animal.speciesCode
false
bridg:Animal.speciesCode
A coded value specifying one of the basic units of biological classification and taxonomic rank that specifies a group of organisms that share similar characteristics and can interbreed with one another to produce fertile offspring.
bridg:Animal.speciesCode
Canis lupus
bridg:Animal.speciesCode
Rattus rattus
bridg:Animal.speciesCode
Assuming this is a two-part name, a "binomial name". The first part of a binomial name is the generic name, the genus of the species. The second part is also called the specific name.
bridg:Animal.speciesCode
urn:AE:Organism.species
bridg:Animal.speciesCode
urn:CTRv1.0:Animal.speciesCode
bridg:Animal.speciesCode
urn:HCTv1.0:CDE_2753243:Therapies.Specify_the_other_source_of_the_preparative_regimen_medication:
bridg:Animal.speciesCode
urn:HCTv1.0:CDE_2960362:Therapies.What_was_the_other_source_of_the_preparative_regimen_medication?
bridg:Animal.speciesCode
urn:HCTv1.0:CDE_2753241:Preparative_Regimen.Specify_the_source_of_the_preparative_regimen_medication:
bridg:Animal.speciesCode
urn:HCTv1.0:CDE_2960357:Therapies.What_was_the_source_of_the_preparative_regimen_medication?
bridg:Animal.speciesCode
urn:HCTv1.0:CDE_2787403:Therapies.Specify_the_ALS__ALG__ATS__ATG_animal_source:
bridg:Animal.speciesCode
urn:HCTv1.0:CDE_2787415:Therapies.Specify_the_ALS__ALG__ATS__ATG_animal_source:x
bridg:Animal.speciesCode
urn:HL7SD:Animal.code
bridg:Animal.speciesCode
urn:HL7SP:Animal.name
bridg:Animal.speciesCode
urn:HL7SP:Animal.code
in IndividualCaseSafetyReport
bridg:Animal.speciesCode
urn:ICSRr2:Animal.code
bridg:Animal.strain
strain
bridg:Animal.strain
false
bridg:Animal.strain
A group of presumed common ancestry with clear-cut physiological but usually not morphological distinctions.
bridg:Animal.strain
Minnesota5 (swine strain)
bridg:Animal.strain
DXL (poultry strain)
bridg:Animal.strain
RB51 (vaccine strain of brucella abortus)
bridg:Animal.strain
The specific genotypic or phenotypic variant of an animal.
bridg:Animal.strain
urn:CTRv1.0:Animal.strain
bridg:Animal.strain
urn:HL7SP:Animal.strainText
bridg:Arm.description
description
bridg:Arm.description
false
bridg:Arm.description
The textual representation of the arm. This is a description of the pathway followed by all subjects, study subjects, or experimental units in a particular treatment regimen.
bridg:Arm.description
Study subjects receive Drug X
bridg:Arm.description
Experimental units receive Placebo
bridg:Arm.description
Study subjects receive drug A IV in the first phase
bridg:Arm.description
drug B Oral in the second phase
bridg:Arm.description
This description should point out what is different between the Arms, if there is more than one Arm.
bridg:Arm.description
urn:C3PR:PlannedArm.description
bridg:Arm.description
urn:C3PR:ScheduledArm.description
bridg:Arm.description
urn:C3PR:Arm.descriptionText
bridg:Arm.description
urn:CTGOV:Arm_Description
bridg:Arm.description
urn:CTRPv1.0:Arm.description
bridg:Arm.description
urn:CTRPv3.8:Arm.description
bridg:Arm.description
urn:CTRRr3:Arm.description
bridg:Arm.description
urn:CTRv1.0:Arm.description
bridg:Arm.description
urn:SDTM_IGv3.1.1:TV.ARM
bridg:Arm.description
urn:SDTM_IGv3.1.1:TA.ARM
bridg:Arm.description
urn:SDTM_IGv3.1.1:DM.ARM
bridg:Arm.description
urn:SDTM_IGv3.1.2:DM.ARM
bridg:Arm.description
urn:SDTM_IGv3.1.2:TV.ARM
bridg:Arm.description
urn:SDTM_IGv3.1.2:TA.ARM
bridg:Arm.description
urn:TDM:StudyDesignArm.description
bridg:Arm.name
name
bridg:Arm.name
false
bridg:Arm.name
A non-unique textual identifier for the arm.
bridg:Arm.name
Treatment A
bridg:Arm.name
urn:C3PR:PlannedArm.name
bridg:Arm.name
urn:C3PR:ScheduledArm.name
bridg:Arm.name
urn:C3PR:Arm.name
bridg:Arm.name
urn:CTGOV:Arm_Number_or_Label
bridg:Arm.name
urn:CTGOV:Arms/Groups
bridg:Arm.name
urn:CTGOV:Group/Cohort_Number_or_Label
bridg:Arm.name
urn:CTOM:StudyParticipantAssignment.armIdentifier
bridg:Arm.name
urn:CTRPv1.0:Arm.name
bridg:Arm.name
urn:CTRPv3.8:Arm.name
bridg:Arm.name
urn:CTRRr3:Arm.name
bridg:Arm.name
urn:CTRv1.0:Arm.name
bridg:Arm.name
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component2/arm.title
bridg:Arm.name
urn:HL7SD:Arm.title
bridg:Arm.name
urn:NCI_CRF_Standard:CDE_2454528v1.0:_Protocol_Arm_Assignment_Text
bridg:Arm.name
urn:SDTM_IGv3.1.1:DM.ARMCD
bridg:Arm.name
urn:SDTM_IGv3.1.1:TA.ARMCD
bridg:Arm.name
urn:SDTM_IGv3.1.1:TV.ARMCD
bridg:Arm.name
urn:SDTM_IGv3.1.2:DM.ARMCD
bridg:Arm.name
urn:SDTM_IGv3.1.2:TV.ARMCD
bridg:Arm.name
urn:SDTM_IGv3.1.2:TA.ARMCD
bridg:Arm.name
urn:TDM:StudyDesignArm.name
bridg:Arm.name
urn:caAERSv2.2:RadiationIntervention.treatmentArm
bridg:Arm.randomizationWeight
randomizationWeight
bridg:Arm.randomizationWeight
false
bridg:Arm.randomizationWeight
The relative proportion of study subjects to be randomized to the arm.
bridg:Arm.randomizationWeight
If 1/3 of study subjects are to be randomized to Arm A and 2/3 to Arm B
bridg:Arm.randomizationWeight
then the values of randomizationWeight for Arms A and B
bridg:Arm.randomizationWeight
respectively
bridg:Arm.randomizationWeight
could be expressed as 1 and 2 or as 1/3 and 2/3.
bridg:Arm.randomizationWeight
urn:CTRv1.0:Arm.randomizationWeight
bridg:Arm.randomizationWeight
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_RANDRAT
bridg:Arm.randomizationWeight
urn:TDM:StudyDesignArm.randomizationWeightForArm
bridg:Arm.targetAccrualNumberRange
targetAccrualNumberRange
bridg:Arm.targetAccrualNumberRange
false
bridg:Arm.targetAccrualNumberRange
An integer falling within minimum and maximum bounds that specifies how many study subjects are to be accrued for the arm.
bridg:Arm.targetAccrualNumberRange
This may represent the minimum number of study subjects needed to support data analysis and/or the maximum number of study subjects that may be accrued to this arm.
bridg:Arm.targetAccrualNumberRange
urn:C3PR:PlannedArm.targetAccrual
bridg:Arm.targetAccrualNumberRange
urn:C3PR:Arm.targetAccrualNumber
bridg:Arm.targetAccrualNumberRange
urn:CTGOV:Number_of_Subjects_per_Treatment_Arm
bridg:Arm.targetAccrualNumberRange
urn:CTRR:Number_of_subjects_per_treatment_arm
bridg:Arm.targetAccrualNumberRange
urn:CTRv1.0:Arm.targetAccrualNumberRange
bridg:Arm.targetAccrualNumberRange
urn:TDM:StudyDesignArm.plannedArmAccrual
bridg:Arm.typeCode
typeCode
bridg:Arm.typeCode
false
bridg:Arm.typeCode
A coded value specifying the kind of arm.
bridg:Arm.typeCode
Experimental
bridg:Arm.typeCode
Active Comparator
bridg:Arm.typeCode
Placebo Comparator
bridg:Arm.typeCode
Sham Comparator
bridg:Arm.typeCode
No intervention
bridg:Arm.typeCode
Other
bridg:Arm.typeCode
urn:CTGOV:Arm_Type
bridg:Arm.typeCode
urn:CTR_Rr2:Number_Treatment_Arms
bridg:Arm.typeCode
urn:CTRPv1.0:Arm.typeCode
bridg:Arm.typeCode
urn:CTRPv3.8:Arm.typeCode
bridg:Arm.typeCode
urn:CTRRr3:Arm.typeCode
bridg:Arm.typeCode
urn:CTRv1.0:Arm.typeCode
bridg:AssessedResultRelationship.typeCode
typeCode
bridg:AssessedResultRelationship.typeCode
false
bridg:AssessedResultRelationship.typeCode
A coded value specifying the kind of assessed result relationship.
bridg:AssessedResultRelationship.typeCode
sequel to
bridg:AssessedResultRelationship.typeCode
component
bridg:AssessedResultRelationship.typeCode
cause
bridg:AssessedResultRelationship.typeCode
urn:CTOM:AssessmentRelationship.typeCode
bridg:AssessedResultRelationship.typeCode
urn:CTRPv3.8:ActivityRelationship.typeCode
bridg:AssessedResultRelationship.typeCode
urn:CTRv1.0:AssessedResultRelationship.typeCode
in IndividualCaseSafetyReport
bridg:AssessedResultRelationship.typeCode
urn:ICSRr2:Component2.typeCode
in R_Product
bridg:AssessedResultRelationship.typeCode
urn:ICSRr2:SequelTo.typeCode
bridg:AssociatedBiologicEntity.typeCode
typeCode
bridg:AssociatedBiologicEntity.typeCode
false
bridg:AssociatedBiologicEntity.typeCode
A coded value specifying the kind of associated biologic entity.
bridg:AssociatedBiologicEntity.typeCode
family member
bridg:AssociatedBiologicEntity.typeCode
roommate
bridg:AssociatedBiologicEntity.typeCode
guardian
bridg:AssociatedBiologicEntity.typeCode
nursing home attendant
bridg:AssociatedBiologicEntity.typeCode
urn:AE:PersonalRelationship.typeCode
bridg:AssociatedBiologicEntity.typeCode
urn:AE:Reporter.relationshipToAEInvestigativeSubject
bridg:AssociatedBiologicEntity.typeCode
urn:CTRv1.0:AssociatedBiologicEntity.typeCode
bridg:AssociatedBiologicEntity.typeCode
urn:HCTv1.0:CDE_2693219:Lab_Results.Who_is_being_tested_for_IDMs?
bridg:AssociatedBiologicEntity.typeCode
urn:HCTv1.0:CDE_2784447:Property_or_Attribute.What_is_the_relationship_of_the_donor_to_the_recipient?
bridg:AssociatedBiologicEntity.typeCode
urn:HCTv1.0:CDE_2705055:Lab_Results.Please_specify_the_person_for_whom_this_typing_is_being_done:
bridg:AssociatedBiologicEntity.typeCode
urn:HCTv1.0:CDE_2728852:Property_or_Attribute.What_is_the_other_relationship_of_the_donor_to_the_recipient:
bridg:AssociatedBiologicEntity.typeCode
urn:HCTv1.0:CDE_2728894:Property_or_Attribute.Specify_the_other_relationship_between_the_donor_and_the_recipient:
bridg:AssociatedBiologicEntity.typeCode
urn:HL7SD:Role.code
bridg:AssociatedBiologicEntity.typeCode
urn:HL7SP:LivingSubject.role
bridg:AssociatedBiologicEntity.typeCode
urn:HL7SP:Role.code
in IndividualCaseSafetyReport
bridg:AssociatedBiologicEntity.typeCode
urn:ICSRr2:Role.code
in IndividualCaseSafetyReport
bridg:AssociatedBiologicEntity.typeCode
urn:ICSRr2:Role2.code
in IndividualCaseSafetyReport
bridg:AssociatedBiologicEntity.typeCode
urn:ICSRr2:ContactParty2.classCode
bridg:Biologic.handlingCode
handlingCode
bridg:Biologic.handlingCode
false
bridg:Biologic.handlingCode
A coded value specifying a special handling requirement for the biologic.
bridg:Biologic.handlingCode
keep at room temperature
bridg:Biologic.handlingCode
store upright
bridg:Biologic.handlingCode
urn:CTRv1.0:Biologic.handlingCode
in R_Product
bridg:Biologic.handlingCode
urn:ICSRr2:Product.handlingCode
bridg:Biologic.riskCode
riskCode
bridg:Biologic.riskCode
false
bridg:Biologic.riskCode
A coded value specifying the type of hazard or threat associated with the biologic.
bridg:Biologic.riskCode
flammable
bridg:Biologic.riskCode
explosive
bridg:Biologic.riskCode
urn:CTRv1.0:Biologic.riskCode
in R_Product
bridg:Biologic.riskCode
urn:ICSRr2:Product.riskCode
bridg:Biologic.stabilityDuration
stabilityDuration
bridg:Biologic.stabilityDuration
false
bridg:Biologic.stabilityDuration
The period of time during which the biologic is considered usable after it is activated (opened).
bridg:Biologic.stabilityDuration
urn:CTRv1.0:Biologic.stabilityDuration
in R_Product
bridg:Biologic.stabilityDuration
urn:ICSRr2:ProductInstance.stabilityTime
bridg:BiologicEntity.actualIndicator
actualIndicator
bridg:BiologicEntity.actualIndicator
false
bridg:BiologicEntity.actualIndicator
Specifies whether the biologic entity is a particular instance (actual) vs. universal kind.
bridg:BiologicEntity.actualIndicator
To indicate a particular BiologicEntity
bridg:BiologicEntity.actualIndicator
actualIndicator = 'true". To indicate a kind of BiologicEntity
bridg:BiologicEntity.actualIndicator
actualIndicator = "false".
bridg:BiologicEntity.actualIndicator
urn:C3PR:StudySubject.actualSubjectIndicator
bridg:BiologicEntity.actualIndicator
urn:CTRv1.0:BiologicEntity.actualIndicator
bridg:BiologicEntity.actualIndicator
urn:HL7SD:PersonKind.determinerCode
Universal
bridg:BiologicEntity.actualIndicator
urn:HL7SD:R_AssignedEntity
choice box.determinerCode
bridg:BiologicEntity.actualIndicator
urn:HL7SD:ExperimentalUnit_ExperimentalUnit2
bridg:BiologicEntity.actualIndicator
urn:HL7SD:NonPersonLivingSubjectKind.determinerCode
in IndividualCaseSafetyReport
bridg:BiologicEntity.actualIndicator
urn:ICSRr2:Animal.determinerCode
in IndividualCaseSafetyReport
bridg:BiologicEntity.actualIndicator
urn:ICSRr2:Person.determinerCode
in IndividualCaseSafetyReport
bridg:BiologicEntity.actualIndicator
urn:ICSRr2:Person2.determinerCode
bridg:BiologicEntity.administrativeGenderCode
administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
false
bridg:BiologicEntity.administrativeGenderCode
A coded value specifying the physical or societal properties by which male is distinguished from female.
bridg:BiologicEntity.administrativeGenderCode
For humans, identification of sex is usually based upon self-report and may come from a form, questionnaire, interview, etc.
bridg:BiologicEntity.administrativeGenderCode
urn:AE:Organism.sex
bridg:BiologicEntity.administrativeGenderCode
urn:C3PR:Participant.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:C3PRv2.9:Participant.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:CDASHv1.1:DM.SEX
bridg:BiologicEntity.administrativeGenderCode
urn:CTOM:Person.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:CTOM:Participant.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:CTOM:Investigator.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:CTRPv1.0:Person.sexCode
bridg:BiologicEntity.administrativeGenderCode
urn:CTRPv3.8:Person.sexCode
bridg:BiologicEntity.administrativeGenderCode
urn:CTRv1.0:BiologicEntity.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:HCTv1.0:CDE_2200604:Recipient_Identification.Gender
bridg:BiologicEntity.administrativeGenderCode
urn:HCTv1.0:CDE_2180389:Physical_Description_of_Individuals.Donor_Gender
bridg:BiologicEntity.administrativeGenderCode
urn:HCTv1.0:CDE_3171628:Physical_Description_of_Individuals.Person_Gender:
bridg:BiologicEntity.administrativeGenderCode
urn:HL7SP:Animal.administrativeGenderCode
in IndividualCaseSafetyReport
bridg:BiologicEntity.administrativeGenderCode
urn:ICSRr2:Animal.administrativeGenderCode
in IndividualCaseSafetyReport
bridg:BiologicEntity.administrativeGenderCode
urn:ICSRr2:Person2.administrativeGenderCode
bridg:BiologicEntity.administrativeGenderCode
urn:LabViewer2.2:ParticipantSex.codeSystem
bridg:BiologicEntity.administrativeGenderCode
urn:LabViewer2.2:ParticipantSex.codeSystemVersion
bridg:BiologicEntity.administrativeGenderCode
urn:LabViewer2.2:ParticipantSex.code
bridg:BiologicEntity.administrativeGenderCode
urn:LabViewer2.2:ParticipantSex.codeSystemName
bridg:BiologicEntity.administrativeGenderCode
urn:LabViewer2.2:ParticipantSex.displayName
bridg:BiologicEntity.administrativeGenderCode
urn:NCI_CRF_Standard:CDE_2200604v3.0:_Person_Gender_Text_Type
bridg:BiologicEntity.administrativeGenderCode
urn:PSC:Participant.gender
bridg:BiologicEntity.administrativeGenderCode
urn:PSCv2.6:Subject.gender
bridg:BiologicEntity.administrativeGenderCode
urn:SDTM_IGv3.1.1:DM.SEX
bridg:BiologicEntity.administrativeGenderCode
urn:SDTM_IGv3.1.2:DM.SEX
bridg:BiologicEntity.administrativeGenderCode
urn:caAERSv2.2:Participant.gender
bridg:BiologicEntity.birthCountryCode
birthCountryCode
bridg:BiologicEntity.birthCountryCode
false
bridg:BiologicEntity.birthCountryCode
A coded value specifying the name of the country in which the biologic entity is born.
bridg:BiologicEntity.birthCountryCode
urn:AE:Organism.birthCountry
bridg:BiologicEntity.birthCountryCode
urn:CTRv1.0:BiologicEntity.birthCountryCode
bridg:BiologicEntity.birthDate
birthDate
bridg:BiologicEntity.birthDate
false
bridg:BiologicEntity.birthDate
The date (and time) on which the biologic entity is born.
bridg:BiologicEntity.birthDate
urn:AE:Organism.birthDate
bridg:BiologicEntity.birthDate
urn:C3PR:Participant.birthDate
bridg:BiologicEntity.birthDate
urn:C3PRv2.9:Participant.birthDate
bridg:BiologicEntity.birthDate
urn:CDASHv1.1:DM.BRTHDAT
bridg:BiologicEntity.birthDate
urn:CDASHv1.1:DM.BRTHDY
bridg:BiologicEntity.birthDate
urn:CDASHv1.1:DM.BRTHTIM
bridg:BiologicEntity.birthDate
urn:CDASHv1.1:DM.BRTHYR
bridg:BiologicEntity.birthDate
urn:CDASHv1.1:DM.BRTHMO
bridg:BiologicEntity.birthDate
urn:CTOM:Investigator.birthDate
bridg:BiologicEntity.birthDate
urn:CTOM:Participant.birthDate
bridg:BiologicEntity.birthDate
urn:CTOM:Person.birthDate
bridg:BiologicEntity.birthDate
urn:CTRPv3.8:Person.birthDate
bridg:BiologicEntity.birthDate
urn:CTRv1.0:BiologicEntity.birthDate
bridg:BiologicEntity.birthDate
urn:HCTv1.0:CDE_2180386:Individuals.Donor_Birth_Date
bridg:BiologicEntity.birthDate
urn:HCTv1.0:CDE_3098934:Individuals.What_is_the_reason_for_the_mother's_missing_age?
bridg:BiologicEntity.birthDate
urn:HCTv1.0:CDE_2883970:Individuals.What_is_the_transplant_donor_or_infant_date_of_birth?
bridg:BiologicEntity.birthDate
urn:HCTv1.0:CDE_2866121:Recipient_Identification.Patient_Date_of_Birth
bridg:BiologicEntity.birthDate
urn:HL7SP:Animal.birthtime
in IndividualCaseSafetyReport
bridg:BiologicEntity.birthDate
urn:ICSRr2:Person2.birthTime
in IndividualCaseSafetyReport
bridg:BiologicEntity.birthDate
urn:ICSRr2:Animal.birthTime
bridg:BiologicEntity.birthDate
urn:Lab:Participant.dateOfBirth
bridg:BiologicEntity.birthDate
urn:Lab:Person.dateOfBirth
bridg:BiologicEntity.birthDate
urn:Lab:Investigator.dateOfBirth
bridg:BiologicEntity.birthDate
urn:LabViewer2.2:Participant.dateOfBirth
bridg:BiologicEntity.birthDate
urn:LabViewer2.2:Person.dateOfBirth
bridg:BiologicEntity.birthDate
urn:NCI_CRF_Standard:CDE_793v5.1:_Person_Birth_Date
bridg:BiologicEntity.birthDate
urn:PSC:Participant.birthDate
bridg:BiologicEntity.birthDate
urn:PSCv2.6:Subject.dateOfBirth
bridg:BiologicEntity.birthDate
urn:SDTM_IGv3.1.1:DM.BRTHDTC
bridg:BiologicEntity.birthDate
urn:SDTM_IGv3.1.2:DM.BRTHDTC
bridg:BiologicEntity.birthDate
urn:caAERSv2.2:Participant.birthDate
bridg:BiologicEntity.birthOrder
birthOrder
bridg:BiologicEntity.birthOrder
false
bridg:BiologicEntity.birthOrder
Indicates the sequence of a biologic entity's birth in the family group.
bridg:BiologicEntity.birthOrder
urn:AE:Organism.birthOrder
bridg:BiologicEntity.birthOrder
urn:CTRv1.0:BiologicEntity.birthOrder
bridg:BiologicEntity.deathDate
deathDate
bridg:BiologicEntity.deathDate
false
bridg:BiologicEntity.deathDate
The date (and time) on which the biologic entity died.
bridg:BiologicEntity.deathDate
This BRIDG SCC reserves the option of re-modeling this in future since death date itself might be better modeled as an observation result and this attribute might better be represented as an uncertaintyCode on that observation result.
bridg:BiologicEntity.deathDate
urn:AE:Organism.deathDate
bridg:BiologicEntity.deathDate
urn:CTOM:DeathSummary.deathDate
bridg:BiologicEntity.deathDate
urn:CTRv1.0:BiologicEntity.deathDate
bridg:BiologicEntity.deathDate
urn:HCTv1.0:CDE_2866512:Occurrences.Date_of_death:
bridg:BiologicEntity.deathDate
urn:HL7SP:Animal.deceasedTime
in IndividualCaseSafetyReport
bridg:BiologicEntity.deathDate
urn:ICSRr2:Person2.deceasedTime
in IndividualCaseSafetyReport
bridg:BiologicEntity.deathDate
urn:ICSRr2:Animal.deceasedTime
bridg:BiologicEntity.deathDateEstimatedIndicator
deathDateEstimatedIndicator
bridg:BiologicEntity.deathDateEstimatedIndicator
false
bridg:BiologicEntity.deathDateEstimatedIndicator
Specifies whether the death date is approximate.
bridg:BiologicEntity.deathDateEstimatedIndicator
This BRIDG SCC reserves the option of re-modeling this in future since death date itself might be better modeled as an observation result and this attribute might better be represented as an uncertaintyCode on that observation result.
bridg:BiologicEntity.deathDateEstimatedIndicator
urn:HCTv1.0:CDE_2768794:Occurrences.If_necessary__please_validate_the_death_date_response
bridg:BiologicEntity.deathIndicator
deathIndicator
bridg:BiologicEntity.deathIndicator
false
bridg:BiologicEntity.deathIndicator
Specifies whether the biologic entity is dead.
bridg:BiologicEntity.deathIndicator
This BRIDG SCC reserves the option of re-modeling this in future since death date itself might be better modeled as an observation result and this attribute might better be represented as an uncertaintyCode on that observation result.
when date is not known but death is known
bridg:BiologicEntity.deathIndicator
urn:CTOM:DeathSummary.deathDate
bridg:BiologicEntity.deathIndicator
urn:CTRv1.0:BiologicEntity.deathIndicator
in IndividualCaseSafetyReport
bridg:BiologicEntity.deathIndicator
urn:ICSRr2:Person2.deceasedInd
in IndividualCaseSafetyReport
bridg:BiologicEntity.deathIndicator
urn:ICSRr2:Animal.deceasedInd
bridg:BiologicEntity.name
name
bridg:BiologicEntity.name
false
bridg:BiologicEntity.name
A non-unique textual identifier for the biologic entity.
bridg:BiologicEntity.name
assumed name of "Mark Twain"
bridg:BiologicEntity.name
official registry name of "Samuel Clemens"
bridg:BiologicEntity.name
customary name of "Sam Clemens"
bridg:BiologicEntity.name
The EN.use attribute of the EN data type is used to distinguish the various types of names, such as official registry, customary, assumed.
bridg:BiologicEntity.name
urn:AE:ContactPerson.name
bridg:BiologicEntity.name
urn:AE:Reporter.personName
bridg:BiologicEntity.name
urn:AE:Receiver.personName
bridg:BiologicEntity.name
urn:C3PR:Person.firstName
bridg:BiologicEntity.name
urn:C3PR:Person.maidenName
bridg:BiologicEntity.name
urn:C3PR:Person.middleName
bridg:BiologicEntity.name
urn:C3PR:Person.lastName
bridg:BiologicEntity.name
urn:C3PRv2.9:StudySubject.otherTreatingPhysician
bridg:BiologicEntity.name
urn:C3PRv2.9:Person.lastName
bridg:BiologicEntity.name
urn:C3PRv2.9:Person.maidenName
bridg:BiologicEntity.name
urn:C3PRv2.9:Person.firstName
bridg:BiologicEntity.name
urn:C3PRv2.9:Person.middleName
bridg:BiologicEntity.name
urn:CTGOV:Facility_Contact_-_Last_Name
bridg:BiologicEntity.name
urn:CTGOV:Facility_Contact_-_Middle_Initial
bridg:BiologicEntity.name
urn:CTGOV:Central_Contact_-_Last_Name
bridg:BiologicEntity.name
urn:CTGOV:Central_Contact_-_Middle_Initial
bridg:BiologicEntity.name
urn:CTGOV:Overall_Study_Officials_-_First_Name
bridg:BiologicEntity.name
urn:CTGOV:Investigators_-_Last_Name
bridg:BiologicEntity.name
urn:CTGOV:Facility_Contact_-_First_Name
bridg:BiologicEntity.name
urn:CTGOV:Investigators_-_Middle_Initial
bridg:BiologicEntity.name
urn:CTGOV:Responsible_Party_-_Name/Official_Title
bridg:BiologicEntity.name
urn:CTGOV:Central_Contact_-_First_Name
bridg:BiologicEntity.name
urn:CTGOV:Overall_Study_Officials_-_Last_Name
bridg:BiologicEntity.name
urn:CTGOV:Investigators_-_First_Name
bridg:BiologicEntity.name
urn:CTGOV:Overall_Study_Officials_-_Middle_Initial
bridg:BiologicEntity.name
urn:CTOM:Participant.middleName
bridg:BiologicEntity.name
urn:CTOM:Person.middleName
bridg:BiologicEntity.name
urn:CTOM:Investigator.middleName
bridg:BiologicEntity.name
urn:CTOM:Person.firstName
bridg:BiologicEntity.name
urn:CTOM:Participant.firstName
bridg:BiologicEntity.name
urn:CTOM:Person.lastName
bridg:BiologicEntity.name
urn:CTOM:Investigator.firstName
bridg:BiologicEntity.name
urn:CTOM:Participant.lastName
bridg:BiologicEntity.name
urn:CTOM:Investigator.lastName
bridg:BiologicEntity.name
urn:CTR_Rr2:IEC_Applicant_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:CTF_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Subcontractor_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Sponsor_Contact_Given_name
bridg:BiologicEntity.name
urn:CTR_Rr2:Subcontractor_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Investigator_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:IEC_Applicant_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:CA_Applicant_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:CA_Applicant_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Network_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Investigator_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Legal_Rep_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Legal_Rep_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:CTF_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Sponsor_Contact_Middle_name
bridg:BiologicEntity.name
urn:CTR_Rr2:Sponsor_Contact_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Investigator_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Legal_Rep_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Network_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:IEC_Applicant_Family_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:CTF_Given_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Network_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:CA_Applicant_Middle_Name
bridg:BiologicEntity.name
urn:CTR_Rr2:Subcontractor_Family_Name
bridg:BiologicEntity.name
urn:CTRPv1.0:Person.name
bridg:BiologicEntity.name
urn:CTRPv3.8:Person.name
bridg:BiologicEntity.name
urn:CTRR:Sponsor
bridg:BiologicEntity.name
urn:CTRR:Principal_Investigator
bridg:BiologicEntity.name
urn:CTRR:Coordinating_investigator
bridg:BiologicEntity.name
urn:CTRR:Secondary_Sponsor
bridg:BiologicEntity.name
urn:CTRR:Financial_Sponsor
bridg:BiologicEntity.name
urn:CTRR:Responsible_Contact_Person
bridg:BiologicEntity.name
urn:CTRR:Site_Representative/_Investigator
bridg:BiologicEntity.name
urn:CTRRr3:Person.name
bridg:BiologicEntity.name
urn:CTRv1.0:BiologicEntity.name
bridg:BiologicEntity.name
urn:HCTv1.0:CDE_3115634:UML_DEFAULT_CD.Mother's_maiden_name:
bridg:BiologicEntity.name
urn:HSDBv1.0:[Sponsor_Contact].Last_Name
bridg:BiologicEntity.name
urn:HSDBv1.0:[Study].Responsible_Party
bridg:BiologicEntity.name
urn:HSDBv1.0:[Principal_Investigator].First_Name
bridg:BiologicEntity.name
urn:HSDBv1.0:[Principal_Investigator]_.Middle_Name
bridg:BiologicEntity.name
urn:HSDBv1.0:[Sponsor_Contact].First_Name
bridg:BiologicEntity.name
urn:HSDBv1.0:[Sponsor_Contact].Middle_Name
bridg:BiologicEntity.name
urn:HSDBv1.0:[Principal_Investigator]_.Last_Name
in E_Organization informational
bridg:BiologicEntity.name
urn:ICSRr2:ContactPerson.name
in IndividualCaseSafetyReport
bridg:BiologicEntity.name
urn:ICSRr2:Person.name
in R_Product
bridg:BiologicEntity.name
urn:ICSRr2:contactPerson.name
in IndividualCaseSafetyReport
bridg:BiologicEntity.name
urn:ICSRr2:Animal.name
in IndividualCaseSafetyReport
bridg:BiologicEntity.name
urn:ICSRr2:Person2.name
bridg:BiologicEntity.name
urn:Lab:Investigator.name
bridg:BiologicEntity.name
urn:LabViewer2.2:Investigator.lastName
bridg:BiologicEntity.name
urn:LabViewer2.2:Investigator.middleName
bridg:BiologicEntity.name
urn:LabViewer2.2:Investigator.firstName
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2179589v2.0:_Person_Given/First_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2179591v2.0:_Person_Family/Last_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2746480v1.0:_Specialist_Physician_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_62749v3.0:_Treating_Physician_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2006163v1.0:_Responsible_Person_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2172v3.0:_Protocol_Registrar_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2740424v1.0:_Treating_Physician_Or_Participating_Investigator_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2179590v2.0:_Person_Middle_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_3008899v1.0:_Reviewer_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2452692v1.0:_Clinical_Research_Associate_Responsible_Person_Name
bridg:BiologicEntity.name
urn:NCI_CRF_Standard:CDE_2006475v2.0:_Individual_Genealogy_Suffix_Code
bridg:BiologicEntity.name
urn:PSC:Participant.firstName
bridg:BiologicEntity.name
urn:PSC:Participant.lastName
bridg:BiologicEntity.name
urn:PSCv2.6:Subject.firstName
bridg:BiologicEntity.name
urn:PSCv2.6:Subject.lastName
bridg:BiologicEntity.name
urn:SDTM_IGv3.1.1:DM.INVNAM
bridg:BiologicEntity.name
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_SPONSOR
bridg:BiologicEntity.name
urn:SDTM_IGv3.1.2:DM.INVNAM
bridg:BiologicEntity.name
urn:WHO:Contact_for_Public_Queries_-_firstname
bridg:BiologicEntity.name
urn:WHO:Primary_Sponsor
bridg:BiologicEntity.name
urn:WHO:Contact_for_Scientific_Queries_-_middlename
s
bridg:BiologicEntity.name
urn:WHO:Secondary_Sponsor
bridg:BiologicEntity.name
urn:WHO:Contact_for_Scientific_Queries_-_lastname
bridg:BiologicEntity.name
urn:WHO:Contact_for_Public_Queries_-_lastname
s of Monetary or Material Support
bridg:BiologicEntity.name
urn:WHO:Source
bridg:BiologicEntity.name
urn:WHO:Contact_for_Scientific_Queries_-_firstname
bridg:BiologicEntity.name
urn:WHO:Contact_for_Public_Queries_-_middlename
bridg:BiologicEntity.name
urn:caAERSv2.2:Person.lastName
bridg:BiologicEntity.name
urn:caAERSv2.2:Person.firstName
bridg:BiologicEntity.name
urn:caAERSv2.2:Recipient.name
bridg:BiologicEntity.name
urn:caAERSv2.2:Participant.maidenName
bridg:BiologicEntity.name
urn:caAERSv2.2:Person.maidenName
bridg:BiologicEntityGroup.actualIndicator
actualIndicator
bridg:BiologicEntityGroup.actualIndicator
false
bridg:BiologicEntityGroup.actualIndicator
Specifies whether the biologic entity group is a particular instance (actual) vs. universal kind.
bridg:BiologicEntityGroup.actualIndicator
To indicate a particular BiologicEntityGroup
bridg:BiologicEntityGroup.actualIndicator
actualIndicator = "true". To indicate a kind of BiologicEntityGroup
bridg:BiologicEntityGroup.actualIndicator
actualIndicator = "false".
bridg:BiologicEntityGroup.actualIndicator
urn:CTRv1.0:BiologicEntityGroup.actualIndicator
choice box.determinerCode
bridg:BiologicEntityGroup.actualIndicator
urn:HL7SD:ExperimentalUnit_ExperimentalUnit2
bridg:BiologicEntityGroup.name
name
bridg:BiologicEntityGroup.name
false
bridg:BiologicEntityGroup.name
A non-unique textual identifier for the biologic entity group.
bridg:BiologicEntityGroup.name
Litter1
bridg:BiologicEntityGroup.name
X12
bridg:BiologicEntityGroup.name
Farmer Brown's Cows
bridg:BiologicEntityGroup.name
urn:AE:Group.name
bridg:BiologicEntityGroup.name
urn:CTRv1.0:BiologicEntityGroup.name
bridg:BiologicEntityGroup.quantity
quantity
bridg:BiologicEntityGroup.quantity
false
bridg:BiologicEntityGroup.quantity
The number of members in a biologic entity group.
bridg:BiologicEntityGroup.quantity
urn:AE:InvestigativeSubject.quantity
bridg:BiologicEntityGroup.quantity
urn:CTRv1.0:BiologicEntityGroup.quantity
bridg:BiologicEntityGroup.quantity
urn:HL7SD:Animal.quantity
bridg:BiologicEntityGroup.quantity
urn:HL7SP:Animal.quantity
in IndividualCaseSafetyReport
bridg:BiologicEntityGroup.quantity
urn:ICSRr2:Animal.quantity
in IndividualCaseSafetyReport
bridg:BiologicEntityGroup.quantity
urn:ICSRr2:Person2.quantity
bridg:BiologicEntityGroup.typeCode
typeCode
bridg:BiologicEntityGroup.typeCode
false
bridg:BiologicEntityGroup.typeCode
A coded value specifying the kind of biologic entity group.
bridg:BiologicEntityGroup.typeCode
litter
bridg:BiologicEntityGroup.typeCode
herd
bridg:BiologicEntityGroup.typeCode
urn:AE:Group.type
bridg:BiologicEntityGroup.typeCode
urn:CTRv1.0:BiologicEntityGroup.typeCode
bridg:BiologicEntityIdentifier.effectiveDateRange
effectiveDateRange
bridg:BiologicEntityIdentifier.effectiveDateRange
false
bridg:BiologicEntityIdentifier.effectiveDateRange
The date (and time) span for when the biologic entity identifier is active.
bridg:BiologicEntityIdentifier.effectiveDateRange
urn:CTRPv1.0:IdentifiedBiologicEntity.statusDateRange
bridg:BiologicEntityIdentifier.effectiveDateRange
urn:CTRPv1.0:IdentifiedBiologicEntity.statusCode
bridg:BiologicEntityIdentifier.effectiveDateRange
urn:CTRv1.0:BiologicEntityIdentifier.effectiveDateRange
bridg:BiologicEntityIdentifier.identifier
identifier
bridg:BiologicEntityIdentifier.identifier
false
bridg:BiologicEntityIdentifier.identifier
A unique symbol that establishes identity of the biologic entity.
bridg:BiologicEntityIdentifier.identifier
medical record number
bridg:BiologicEntityIdentifier.identifier
This is different from the SubjectIdentifier.identifier.
bridg:BiologicEntityIdentifier.identifier
urn:AE:PersonIdentifier.sponsoringOrganization
bridg:BiologicEntityIdentifier.identifier
urn:AE:PersonIdentifier.identifier
bridg:BiologicEntityIdentifier.identifier
urn:C3PR:Participant.identifiers
bridg:BiologicEntityIdentifier.identifier
urn:C3PR:ResearchStaff.nciIdentifier
bridg:BiologicEntityIdentifier.identifier
urn:CTRPv1.0:IdentifiedBiologicEntity.identifier
bridg:BiologicEntityIdentifier.identifier
urn:CTRPv3.8:Person.identifier
bridg:BiologicEntityIdentifier.identifier
urn:CTRPv3.8:IdentifiedEntity.assignedIdentifier
bridg:BiologicEntityIdentifier.identifier
urn:CTRv1.0:BiologicEntityIdentifier.identifier
bridg:BiologicEntityIdentifier.identifier
urn:HCTv1.0:MD_Anderson_Specific_Content:_Recipient.Recipient_medical_record_number
bridg:BiologicEntityIdentifier.identifier
urn:HCTv1.0:CDE_2958200:Individuals.IUBMID__
CRID Universal Recipient ID
bridg:BiologicEntityIdentifier.identifier
urn:HCTv1.0:CDE_2527897:Recipient_Identification.CIBMTR_recipient_ID
bridg:BiologicEntityIdentifier.identifier
urn:HCTv1.0:CDE_2735593:Individuals.Non-NMDP_donor_ID:
bridg:BiologicEntityIdentifier.identifier
urn:HCTv1.0:CDE_2220102:Individuals.Social_Security_Number
bridg:BiologicEntityIdentifier.identifier
urn:HCTv1.0:CDE_2729076:Specimen_Characteristics.Research_sample_recipient_ID:
bridg:BiologicEntityIdentifier.identifier
urn:HL7SD:Animal.id
bridg:BiologicEntityIdentifier.identifier
urn:HL7SP:Animal.id
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier.identifier
urn:ICSRr2:IdentifiedEntity3.id
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier.identifier
urn:ICSRr2:IdentifiedEntity2.id
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier.identifier
urn:ICSRr2:IdentifiedEntity.id
bridg:BiologicEntityIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2465308v1.0:_Patient_Multiple_Clinical_Trials_Cooperative_Group_Identifier_Number
bridg:BiologicEntityIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2746468v1.0:_Healthcare_Facility_Participant_Identifier
bridg:BiologicEntityIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2822790v1.0:_Participant_Prior_Clinical_Study_Identifier
bridg:BiologicEntityIdentifier.identifier
urn:PSC:Participant.personId
bridg:BiologicEntityIdentifier.identifier
urn:PSCv2.6:Subject.personId
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
missingIdentifierReasonCode
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
false
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
A coded value specifying why the identifier was not provided.
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
forgot to ask
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
subject refused
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
This value should only be populated if BiologicEntityIdentifier.identifier is null.
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
urn:HCTv1.0:CDE_3115593:Individuals.If_necessary__please_validate_the_Social_Security_number_response:
bridg:BiologicEntityIdentifier.missingIdentifierReasonCode
urn:HCTv1.0:CDE_3115786:Individuals.If_necessary__please_validate_patient_identifier_response.
bridg:BiologicEntityIdentifier.typeCode
typeCode
bridg:BiologicEntityIdentifier.typeCode
false
bridg:BiologicEntityIdentifier.typeCode
A coded value specifying the kind of biologic entity identifier.
bridg:BiologicEntityIdentifier.typeCode
hospital record number
bridg:BiologicEntityIdentifier.typeCode
medical record number
bridg:BiologicEntityIdentifier.typeCode
urn:AE:PersonIdentifier.identifierType
bridg:BiologicEntityIdentifier.typeCode
urn:CTRPv1.0:IdentifiedBiologicEntity.typeCode
bridg:BiologicEntityIdentifier.typeCode
urn:CTRv1.0:BiologicEntityIdentifier.typeCode
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier.typeCode
urn:ICSRr2:IdentifiedEntity.code
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier.typeCode
urn:ICSRr2:IdentifiedEntity2.code
in IndividualCaseSafetyReport
bridg:BiologicEntityIdentifier.typeCode
urn:ICSRr2:IdentifiedEntity3.code
bridg:BiologicEntityPart.anatomicSiteCode
anatomicSiteCode
bridg:BiologicEntityPart.anatomicSiteCode
false
bridg:BiologicEntityPart.anatomicSiteCode
A coded value specifying the anatomic location or system of the biologic entity part.
bridg:BiologicEntityPart.anatomicSiteCode
eye
bridg:BiologicEntityPart.anatomicSiteCode
skin
bridg:BiologicEntityPart.anatomicSiteCode
kidney
bridg:BiologicEntityPart.anatomicSiteCode
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:BiologicEntityPart.anatomicSiteCode
urn:CTRv1.0:BiologicEntityPart.anatomicSiteCode
bridg:BiologicEntityPart.anatomicSiteCode
urn:HL7SD:Access.targetSiteCode
bridg:BiologicEntityPart.anatomicSiteLateralityCode
anatomicSiteLateralityCode
bridg:BiologicEntityPart.anatomicSiteLateralityCode
false
bridg:BiologicEntityPart.anatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) where the anatomic site is in a biologic entity part.
bridg:BiologicEntityPart.anatomicSiteLateralityCode
left
bridg:BiologicEntityPart.anatomicSiteLateralityCode
right
bridg:BiologicEntityPart.anatomicSiteLateralityCode
both
bridg:BiologicEntityPart.anatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:BiologicEntityPart.anatomicSiteLateralityCode
urn:CTRv1.0:BiologicEntityPart.anatomicSiteLateralityCode
bridg:BiologicEntityPart.anatomicSiteLateralityCode
urn:HL7SD:Access.targetSiteCode
bridg:BiologicEntityPart.quantityRange
quantityRange
bridg:BiologicEntityPart.quantityRange
false
bridg:BiologicEntityPart.quantityRange
An integer falling within minimum and maximum bounds that specifies how many parts that need to be present.
bridg:BiologicEntityPart.quantityRange
2 Skin patches
bridg:BiologicEntityPart.quantityRange
Default is 1. Normally used during study design to indicate number of parts that will be used in a study. For example 100 study subjects with 3-5 skin patches.
bridg:BiologicEntityPart.quantityRange
urn:CTRv1.0:BiologicEntityPart.quantity
bridg:CompanionStudyRelationship.registrationRequiredIndicator
registrationRequiredIndicator
bridg:CompanionStudyRelationship.registrationRequiredIndicator
false
bridg:CompanionStudyRelationship.registrationRequiredIndicator
Specifies whether registration to the companion study is mandatory when registering to the parent study.
bridg:CompanionStudyRelationship.registrationRequiredIndicator
urn:C3PRv2.9:CompanionStudyAssociation.mandatoryIndicator
bridg:CompanionStudyRelationship.registrationRequiredIndicator
urn:CTRv1.0:CompanionStudyRelationship.registrationRequiredIndicator
bridg:Cosmetic.stabilityDuration
stabilityDuration
bridg:Cosmetic.stabilityDuration
false
bridg:Cosmetic.stabilityDuration
The period of time during which the cosmetic is considered usable after it is activated (opened).
bridg:Cosmetic.stabilityDuration
urn:CTRv1.0:Cosmetic.stabilityDuration
in R_Product
bridg:Cosmetic.stabilityDuration
urn:ICSRr2:ProductInstance.stabilityTime
bridg:DataMonitoringCommitteeCharterVersion.description
description
bridg:DataMonitoringCommitteeCharterVersion.description
false
bridg:DataMonitoringCommitteeCharterVersion.description
A textual explanation of the contents of the data monitoring committee charter.
bridg:DataMonitoringCommitteeCharterVersion.description
"Data will be presented via blinded summaries and listings in PDF format
bridg:DataMonitoringCommitteeCharterVersion.description
with additional availability of unblinded patient profiles in electronic format. The following is a description of the data to be included in the summaries and listings¦
bridg:DataMonitoringCommitteeCharterVersion.description
If the charter is about meeting schedules
bridg:DataMonitoringCommitteeCharterVersion.description
then the description could be
bridg:DataMonitoringCommitteeCharterVersion.description
"Meetings will be held monthly
bridg:DataMonitoringCommitteeCharterVersion.description
beginning 6 weeks after the first subject's first visit."
bridg:DataMonitoringCommitteeCharterVersion.description
urn:Statistics_v1.0:DataMonitoringCommitteeCharter.description
bridg:DefinedActivity.categoryCode
categoryCode
bridg:DefinedActivity.categoryCode
false
bridg:DefinedActivity.categoryCode
A coded value specifying a classification of activities.
bridg:DefinedActivity.categoryCode
In the case where categoryCode = "anti-cancer treatment"
bridg:DefinedActivity.categoryCode
the subcategoryCode may = "radiotherapy"
bridg:DefinedActivity.categoryCode
and the nameCode may = "external beam radiotherapy".
bridg:DefinedActivity.categoryCode
In Procedure
bridg:DefinedActivity.categoryCode
categoryCode may = "abdominal surgery".
bridg:DefinedActivity.categoryCode
In AdministrativeActivity
bridg:DefinedActivity.categoryCode
the categoryCode may = "Disposition" (off study
bridg:DefinedActivity.categoryCode
epoch completion)
bridg:DefinedActivity.categoryCode
"Milestone" (informed consent
bridg:DefinedActivity.categoryCode
enrollment
bridg:DefinedActivity.categoryCode
registry
bridg:DefinedActivity.categoryCode
randomization) or "Other" (unblinding) activities.
bridg:DefinedActivity.categoryCode
For lab procedures
bridg:DefinedActivity.categoryCode
categoryCode may = "hematology"
bridg:DefinedActivity.categoryCode
"urinalysis"
bridg:DefinedActivity.categoryCode
or "chemistry".
bridg:DefinedActivity.categoryCode
Theoretically speaking, the categoryCode should be derivable from the subcategoryCode, however if there may only be a category and not a subcategory, then both attributes must be present in the model.
When value sets are defined for this attribute, we may need to move it to the DefinedActivity subclasses so that the different value domains can be bound to the correct subclass.
bridg:DefinedActivity.categoryCode
urn:CDASHv1.1:IE.IECAT
bridg:DefinedActivity.categoryCode
urn:CDASHv1.1:MH.MHCAT
bridg:DefinedActivity.categoryCode
urn:CDASHv1.1:DA.DACAT
bridg:DefinedActivity.categoryCode
urn:CDASHv1.1:LB.LBCAT
bridg:DefinedActivity.categoryCode
urn:CDASHv1.1:SU.SUCAT
bridg:DefinedActivity.categoryCode
urn:CTOM:Activity.type
bridg:DefinedActivity.categoryCode
urn:CTOM:Procedure.type
bridg:DefinedActivity.categoryCode
urn:CTOM:SubstanceAdministration.name
bridg:DefinedActivity.categoryCode
urn:CTOM:SubstanceAdministration.type
bridg:DefinedActivity.categoryCode
urn:CTOM:Imaging.type
bridg:DefinedActivity.categoryCode
urn:CTOM:SpecimenAcquisition.type
bridg:DefinedActivity.categoryCode
urn:CTOM:Radiation.type
bridg:DefinedActivity.categoryCode
urn:CTRPv1.0:PlannedEligibilityCriterion.categoryCode
bridg:DefinedActivity.categoryCode
urn:CTRPv1.0:SubstanceAdministration.categoryCode
bridg:DefinedActivity.categoryCode
urn:CTRPv1.0:PlannedObservation.categoryCode
bridg:DefinedActivity.categoryCode
urn:CTRPv1.0:InterventionalStudyProtocol.interventionTypeCode
bridg:DefinedActivity.categoryCode
urn:CTRPv1.0:PlannedActivity.categoryCode
bridg:DefinedActivity.categoryCode
urn:CTRPv1.0:Activity.categoryCode
bridg:DefinedActivity.categoryCode
urn:CTRPv3.8:Activity.categoryCode
bridg:DefinedActivity.categoryCode
urn:CTRv1.0:DefinedActivity.categoryCode
bridg:DefinedActivity.categoryCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Observation.code
bridg:DefinedActivity.categoryCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.code
bridg:DefinedActivity.categoryCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Procedure.code
bridg:DefinedActivity.categoryCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Encounter.code
bridg:DefinedActivity.categoryCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Act.code
bridg:DefinedActivity.categoryCode
urn:Lab:SubjectAssignment.type
bridg:DefinedActivity.categoryCode
urn:Lab:Activity.typeModifier
bridg:DefinedActivity.categoryCode
urn:LabViewer2.2:Activity.type
bridg:DefinedActivity.categoryCode
urn:PSC:ActivityType.name
bridg:DefinedActivity.categoryCode
urn:PSCv2.6:ActivityType.name
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:CM.CMCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:IE.IECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:TI.IECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:SC.SCCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:VS.VSCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:QS.QSCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:EX.EXCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:DA.DACAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:PE.PECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:MH.MHCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:SU.SUCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:EG.EGCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:LB.LBCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.1:DS.DSCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:CE.CECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:EG.EGCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:PC.PCCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:PE.PECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:DA.DACAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:TI.IECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:FA.FACAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:MS.MSCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:SU.SUCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:SC.SCCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:LB.LBCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:QS.QSCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:CM.CMCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:EX.EXCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:VS.VSCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:IE.IECAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:PP.PPCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:MB.MBCAT
bridg:DefinedActivity.categoryCode
urn:SDTM_IGv3.1.2:MH.MHCAT
bridg:DefinedActivity.description
description
bridg:DefinedActivity.description
false
bridg:DefinedActivity.description
The textual representation of the activity.
bridg:DefinedActivity.description
This may contain more detail than the description present in the text part of a coded concept.
bridg:DefinedActivity.description
urn:AE:ProductInvestigation.description
bridg:DefinedActivity.description
urn:BRIDGv2.2:ExperimentalUnitAllocationMethod.description
bridg:DefinedActivity.description
urn:CTOM:Surgery.descriptionText
bridg:DefinedActivity.description
urn:CTOM:SpecimenAcquisition.descriptionText
bridg:DefinedActivity.description
urn:CTOM:Activity.descriptionText
bridg:DefinedActivity.description
urn:CTOM:Procedure.descriptionText
bridg:DefinedActivity.description
urn:CTOM:Imaging.descriptionText
bridg:DefinedActivity.description
urn:CTOM:Radiation.descriptionText
bridg:DefinedActivity.description
urn:CTOM:Histopathology.reportDescriptiveText
bridg:DefinedActivity.description
urn:CTRPv1.0:Activity.textDescription
bridg:DefinedActivity.description
urn:CTRPv1.0:PlannedObservation.textDescription
bridg:DefinedActivity.description
urn:CTRPv1.0:SubstanceAdministration.textDescription
bridg:DefinedActivity.description
urn:CTRPv1.0:PlannedEligibilityCriterion.textDescription
bridg:DefinedActivity.description
urn:CTRPv1.0:PlannedActivity.textDescription
bridg:DefinedActivity.description
urn:CTRPv3.8:Intervention.descriptionText
bridg:DefinedActivity.description
urn:CTRRr3:DefinedActivity.description
bridg:DefinedActivity.description
urn:CTRv1.0:DefinedActivity.description
bridg:DefinedActivity.description
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol//plannedStudy/precondition/eligibilityCriterion.text
bridg:DefinedActivity.description
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Observation.text
bridg:DefinedActivity.description
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.text
bridg:DefinedActivity.description
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Procedure.text
bridg:DefinedActivity.description
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Encounter.text
bridg:DefinedActivity.description
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Act.text
bridg:DefinedActivity.description
urn:HL7SD:EligibilityCriterion.text
in R_Product
bridg:DefinedActivity.description
urn:ICSRr2:TransportationEvent.text
in R_Product
bridg:DefinedActivity.description
urn:ICSRr2:ProductEvent.text
bridg:DefinedActivity.description
urn:Lab:LabTest.additionalTestDescription
bridg:DefinedActivity.description
urn:LabViewer2.2:LaboratoryTest.additionalDescription
bridg:DefinedActivity.description
urn:PSC:Activity.description
bridg:DefinedActivity.description
urn:PSCv2.6:ScheduledActivity.details
bridg:DefinedActivity.description
urn:PSCv2.6:Activity.description
bridg:DefinedActivity.description
urn:SDTM_IGv3.1.1:SE.ELEMENT
bridg:DefinedActivity.description
urn:SDTM_IGv3.1.1:SV.SVUPDES
bridg:DefinedActivity.description
urn:SDTM_IGv3.1.2:TA.ELEMENT
bridg:DefinedActivity.description
urn:SDTM_IGv3.1.2:SV.SVUPDES
bridg:DefinedActivity.description
urn:SDTM_IGv3.1.2:SE.ELEMENT
bridg:DefinedActivity.description
urn:SDTM_IGv3.1.2:TE.ELEMENT
bridg:DefinedActivity.description
urn:TDM:TDMPlannedActivity.description
bridg:DefinedActivity.description
urn:caAERSv2.2:SurgeryIntervention.description
bridg:DefinedActivity.description
urn:caAERSv2.2:TreatmentInformation.treatmentDescription
bridg:DefinedActivity.description
urn:caAERSv2.2:RadiationIntervention.description
bridg:DefinedActivity.description
urn:caAERSv2.2:TreatmentAssignment.description
bridg:DefinedActivity.nameCode
nameCode
bridg:DefinedActivity.nameCode
false
bridg:DefinedActivity.nameCode
A coded value specifying the non-unique textual identifier for the activity.
bridg:DefinedActivity.nameCode
CPT4 or SNOMED term for a surgical procedure.
bridg:DefinedActivity.nameCode
Coded value for a single analytic procedure in a lab test.
bridg:DefinedActivity.nameCode
The code and text of an individual question on the eligibility checklist of a protocol.
bridg:DefinedActivity.nameCode
The textual description of the activity is captured in the complex data type CD.
bridg:DefinedActivity.nameCode
urn:AE:ProductObservation.typeCode
bridg:DefinedActivity.nameCode
urn:C3PR:StratificationCriterion.questionText
bridg:DefinedActivity.nameCode
urn:C3PR:EligbilityCriterion.questionText
bridg:DefinedActivity.nameCode
urn:C3PRv2.9:EligibilityCriteria.questionText
bridg:DefinedActivity.nameCode
urn:C3PRv2.9:Arm.name
bridg:DefinedActivity.nameCode
urn:C3PRv2.9:SolicitedAdverseEvent
bridg:DefinedActivity.nameCode
urn:C3PRv2.9:StratificationCriterion.questionText
bridg:DefinedActivity.nameCode
urn:C3PRv2.9:ScheduledEpoch.scEpochWorkflowStatus
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:LB.LBTEST
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:PE.PETEST
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:AE.AEACNOTH
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:AE.AEACN
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:IE.IETEST
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:IE.IETESTCD
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:SC.SCTEST
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:DA.DATEST
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:EG.EGTEST
bridg:DefinedActivity.nameCode
urn:CDASHv1.1:VS.VSTEST
bridg:DefinedActivity.nameCode
urn:CTOM:Procedure.name
bridg:DefinedActivity.nameCode
urn:CTOM:ClinicalResult.panelName
bridg:DefinedActivity.nameCode
urn:CTOM:Diagnosis.name
bridg:DefinedActivity.nameCode
urn:CTOM:Surgery.name
bridg:DefinedActivity.nameCode
urn:CTOM:Activity.name
bridg:DefinedActivity.nameCode
urn:CTOM:SpecimenAcquisition.name
bridg:DefinedActivity.nameCode
urn:CTOM:AdverseEventTherapy.id
bridg:DefinedActivity.nameCode
urn:CTOM:AdverseEvent.actionTakenCode
bridg:DefinedActivity.nameCode
urn:CTOM:Imaging.name
bridg:DefinedActivity.nameCode
urn:CTOM:Radiation.name
bridg:DefinedActivity.nameCode
urn:CTR_Rr2:Principal_inclusion_criteria
bridg:DefinedActivity.nameCode
urn:CTR_Rr2:Principal_exclusion_criteria
bridg:DefinedActivity.nameCode
urn:CTRPv1.0:PlannedEligibilityCriterion.alternateName
bridg:DefinedActivity.nameCode
urn:CTRPv1.0:PlannedActivity.alternateName
bridg:DefinedActivity.nameCode
urn:CTRPv1.0:PlannedObservation.alternateName
bridg:DefinedActivity.nameCode
urn:CTRPv1.0:SubstanceAdministration.nameCode
bridg:DefinedActivity.nameCode
urn:CTRPv3.8:PerformedActivity.nameCode
bridg:DefinedActivity.nameCode
urn:CTRPv3.8:PerformedActivity.name
bridg:DefinedActivity.nameCode
urn:CTRPv3.8:PlannedActivity.name
bridg:DefinedActivity.nameCode
urn:CTRR:Intervention_Name
bridg:DefinedActivity.nameCode
urn:CTRRr3:DefinedActivity.nameCode
bridg:DefinedActivity.nameCode
urn:CTRv1.0:DefinedActivity.nameCode
bridg:DefinedActivity.nameCode
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component4/timePointEventDefinition.code
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2875714:Therapies.Classify_the_preparative_regimen:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2673840:Therapies.Specify_the_other_planned_post-HSCT_therapy:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2773880:Therapies.Specify_other_treatment_that_the_donor_received_to_enhance_the_product_collection:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2936192:Lab_Results.Specify_the_type_of_test_used_for_BCR/ABL_or_other_molecular_markers:
HSCT therapy?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2738487:Therapies.What_was_the_type_of_post-hematopoietic_stem_cell_transplantation
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2932826:Therapies.Specify_treatment:
s given for central nervous system:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2761989:Therapies.Specify_treatment
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2403909:Therapies.Other__specify_-_rad
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2705055:Lab_Results.Please_specify_the_person_for_whom_this_typing_is_being_done:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2744936:Techniques.Other_manipulation_specify:
CML: Part 1 of 2.What type of treatment did the recipient receive prior to the hematopoietic stem cell transplantation (HSCT?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2737666:Chronic_Myelogenous_Leukemia
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2769634:Adverse_Events.Specify_other_most_likely_cause_of_the_adverse_event:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2934733:Organism.Specify_the_infection_organism:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2762041:Therapies.Specify_other_central_nervous_system_type_of_treatment_given:
s were used?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2932822:Therapies.Which_treatment
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2963496:Lab_Results.Specify_the_bone_marrow_procedure_performed:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2682940:Lab_Results.For_the_systemic_lupus_erythematosus__specify_the_other_antibody:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2936196:Lab_Results.Specify_other_BCR/ABL_or_other_molecular_testing_performed:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2769592:Procedures.What_is_the_reserved_portion_end_point?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2963613:Procedures.What_type_of_excisional_biopsy/surgical_procedure_was_performed?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_65292_-:Therapies.Therapy_type_other_specify
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2980360:Therapies.What_type_of_surgical_procedure_was_performed?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2756917:Lab_Results.Type_of_immunologic_laboratory_procedure_performed:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2980753:Therapies.Specify_the_treatment_given:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2793799:Diagnosis.Diagnosis_of_chronic_GVHD_was_based_on:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2934613:Organism.Select_the_infection_organism:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2630451:Procedures.Specify_test_and_method_for_test_performed_on_other_infectious_disease_marker:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_3061476:Therapies.Specify_other_treatment:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2749868:Lab_Results.For_the_antiphospholipid_syndrome__what_was_the_laboratory_procedure_type?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2467549:Therapies.Type_of_Procedure
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2980793:Therapies.Specify_the_therapeutic_procedure_administered:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_3087995:Therapies.Specify_the_other_systemic_and_or_intrathecal_therapy_administered:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2749874:Lab_Results.For_the_wegener_granulomatosis__what_was_the_laboratory_procedure_type?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2201768:Medical_Imaging.Type_of_imaging
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_3108801:Therapies.Specify_other_reserved_portion_end_point
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2801066:Diagnosis.Specify_the_diagnosis_of_liver_toxicity_by_the_type_of_clinical_signs__symptoms_or_evaluation:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2729156:Lab_Results.What_is_the_hematopoietic_stem_sell_graft_timepoint_type_at_laboratory_procedure?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2980366:Therapies.Specify_the_surgical_procedure_performed:
CML: Part 1 of 2.Specify the other type of therapy that the recipient received prior to this hematopoietic stem cell transplantation (HSCT:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2738393:Chronic_Myelogenous_Leukemia
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2969578:Lab_Results.Specify_tumor_marker_laboratory_procedure_performed:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2705093:Lab_Results.Specify_person_and_typing:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2797534:Diagnosis.Specify_the_clinical_sign__symptom_or_evaluation_used_to_diagnose_liver_toxicity:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2787410:Therapy_Results.What_is_the_follow-up_timepoint_of_this_form?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2762109:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_other_organism_:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2749880:Lab_Results.For_the_polyarteritis_nodosa__classical_or_microscopic__what_was_the_laboratory_procedure_type?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2749841:Lab_Results.For_the_systemic_sclerosis__what_was_the_laboratory_procedure_type?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2772167:Therapies.Specify_the_other_growth_factor_treatment_that_the_donor_received_to_enhance_the_product_collection:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2770346:Procedures.Specify_the_other_diagnostic_procedure:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2797522:Therapies.Specify_the_treatment_received_for_VOD:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2426129:Therapies.Other__specify_-_chem
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_3102448:Therapies.Specify_the_other_systemic_therapy_administered:
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2953828:Therapies.Specify_the_other_immune_therapy
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2769598:Adverse_Events.What_is_the_most_likely_cause_of_the_adverse_event?
bridg:DefinedActivity.nameCode
urn:HCTv1.0:CDE_2978238:Surgery.Specify_other_surgical_procedure
in IndividualCaseSafetyReport
bridg:DefinedActivity.nameCode
urn:ICSRr2:CausalityAssessment.code
in R_Product
bridg:DefinedActivity.nameCode
urn:ICSRr2:TransportationEvent.code
in R_Product
bridg:DefinedActivity.nameCode
urn:ICSRr2:ProductEvent.code
in IndividualCaseSafetyReport
bridg:DefinedActivity.nameCode
urn:ICSRr2:ProductDefectAssessment.code
bridg:DefinedActivity.nameCode
urn:LabViewer2.2:SubjectAssignment.type
bridg:DefinedActivity.nameCode
urn:LabViewer2.2:LaboratoryTestIdentifier.codeSystemName
bridg:DefinedActivity.nameCode
urn:LabViewer2.2:LaboratoryTestIdentifier.codeSystemVersion
bridg:DefinedActivity.nameCode
urn:LabViewer2.2:LaboratoryTestIdentifier.codeSystem
bridg:DefinedActivity.nameCode
urn:LabViewer2.2:LaboratoryTestIdentifier.displayName
bridg:DefinedActivity.nameCode
urn:LabViewer2.2:LaboratoryTestIdentifier.code
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_3608v4.0:_Study_Stratification_Text
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_2435042v1.2:_Protocol_Deviation_Action_Text
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_3437657v1.0:_Concomitant_Medication_Form_Data_Collection_Use_Reason
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_2003746v5.0:_Laboratory_Finding_Test_Name
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_2847352v1.0:_Disease_Staging_Timepoint_Name
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_2179892v1.0:_Adverse_Event_Cancer_Treatment_Related_Type
bridg:DefinedActivity.nameCode
urn:NCI_CRF_Standard:CDE_2201348v1.0:_Adverse_Event_Suspected_Other_Attribution_Text_Name
bridg:DefinedActivity.nameCode
urn:PSC:Activity.name
bridg:DefinedActivity.nameCode
urn:PSCv2.6:Activity.code
bridg:DefinedActivity.nameCode
urn:PSCv2.6:Source.name
bridg:DefinedActivity.nameCode
urn:PSCv2.6:Activity.name
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:AE.AEACN
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:DS.DSTERM
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:PE.PETEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:AE.AEACNOTH
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:QS.QSTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:EG.EGTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:SE.ETCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:SC.SCTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:VS.VSTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:TI.TITEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:VS.VSTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:PE.PETESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:EG.EGTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:SC.SCTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:IE.IETEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:QS.QSTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:EX.EXTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:IE.IETESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:LB.LBTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:DA.DATEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:LB.LBTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.1:DA.DATESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:IE.IETEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:QS.QSTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PC.PCTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TE.ETCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MS.MSTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:IE.IETESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TI.IETEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:EG.EGTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSPARMCD_where_TSPARMCD_CURTRT
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:QS.QSTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:DA.DATEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MS.MSTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:EG.EGTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MS.MSTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PC.PCTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MS.MSLOINC
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_RANDSTR
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:FA.FATESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:SC.SCTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:VS.VSTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PE.PETESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:VS.VSTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MB.MBTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:DA.DATESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSPARM_where_TSPARMCD_RANDSTR
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:FA.FATEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:VS.VSTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:LB.LBTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:AE.AEACN
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:AE.AEACNOTH
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:LB.LBTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_CURTRT
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:QS.QSTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:SE.SEUPDES
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MB.MBTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:LB.LBTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:SE.ETCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PE.PETEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PC.PCTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:EG.EGTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TA.ETCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSPARM_where_TSPARMCD_CURTRT
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:EX.EXTPTREF
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSPARMCD_where_TSPARMCD_RANDSTR
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:SC.SCTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_AGEMIN
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:MB.MBLOINC
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:LB.LBLOINC
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:TI.IETESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PP.PPTEST
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:AE.AECONTRT
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:PP.PPTESTCD
bridg:DefinedActivity.nameCode
urn:SDTM_IGv3.1.2:CE.CEOCCUR
bridg:DefinedActivity.nameCode
urn:TDM:TDMPlannedActivity.codedDescription
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:Therapy.name
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:StudyParticipantPreExistingCondition___PriorTherapy.meddraCode
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:CtcTerm.select___SolicitedAdverseEvent
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:SAEReportPriorTherapy.other
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:StudyParticipantPreExistingCondition___PriorTherapy.text
meddraTerm
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___SolicitedAdverseEvent
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:CtcTerm.ctepCode___SolicitedAdverseEvent
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:Lab___LabTerm
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:StudyParticipantPriorTherapy.other
otherTerm
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___SolicitedAdverseEvent
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:TreatmentAssignment.code
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:Study___AbstractExpectedAE
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:SAEReportPreExistingCondition___PriorTherapy.meddraCode
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:StudyParticipantPreExistingCondition___PriorTherapy.meddraTerm
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:SAEReportPreExistingCondition___PriorTherapy.text
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:CtcTerm.term___SolicitedAdverseEvent
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:Lab.other
bridg:DefinedActivity.nameCode
urn:caAERSv2.2:SAEReportPreExistingCondition___PriorTherapy.meddraTerm
bridg:DefinedActivity.repeatDuration
repeatDuration
bridg:DefinedActivity.repeatDuration
true
bridg:DefinedActivity.repeatDuration
The period of time over which the activity is repeated.
bridg:DefinedActivity.repeatDuration
Derived from repeatQuantity and repeatFrequencyCode or repeatFrequencyRatio (constraint allows only one). In any given implementation, if quantity is not provided, duration may be provided instead, however the BRIDG team determined that quantity is considered more fundamental for a domain analysis model.
bridg:DefinedActivity.repeatDuration
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatDuration
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatDuration
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatDuration
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatDuration
urn:CTRv1.0:DefinedActivity.repeatDuration
bridg:DefinedActivity.repeatDuration
urn:TDM:CyclingRule
bridg:DefinedActivity.repeatFrequencyCode
repeatFrequencyCode
bridg:DefinedActivity.repeatFrequencyCode
false
bridg:DefinedActivity.repeatFrequencyCode
A coded value specifying the number of occurrences of an activity within a given time period.
bridg:DefinedActivity.repeatFrequencyCode
BID = Two times per day
bridg:DefinedActivity.repeatFrequencyCode
at unspecified times (does not necessarily imply that these are 12 hours apart)
bridg:DefinedActivity.repeatFrequencyCode
Q12H = Every twelve hours
bridg:DefinedActivity.repeatFrequencyCode
urn:C3PRv2.9:PlannedNotification.frequency
bridg:DefinedActivity.repeatFrequencyCode
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyCode
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyCode
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyCode
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyCode
urn:CTRv1.0:DefinedActivity.repeatFrequencyCode
bridg:DefinedActivity.repeatFrequencyCode
urn:TDM:CyclingRule
bridg:DefinedActivity.repeatFrequencyRatio
repeatFrequencyRatio
bridg:DefinedActivity.repeatFrequencyRatio
false
bridg:DefinedActivity.repeatFrequencyRatio
A ratio representing the number of occurrences of an activity within a given time period.
bridg:DefinedActivity.repeatFrequencyRatio
Once per 12 hours
bridg:DefinedActivity.repeatFrequencyRatio
2 times per day
bridg:DefinedActivity.repeatFrequencyRatio
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyRatio
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyRatio
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyRatio
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatFrequencyRatio
urn:CTRv1.0:DefinedActivity.repeatFrequencyRatio
bridg:DefinedActivity.repeatFrequencyRatio
urn:TDM:CyclingRule
bridg:DefinedActivity.repeatQuantityRange
repeatQuantityRange
bridg:DefinedActivity.repeatQuantityRange
false
bridg:DefinedActivity.repeatQuantityRange
An integer falling within minimum and maximum bounds that specifies how many times the activity occurs.
bridg:DefinedActivity.repeatQuantityRange
If the frequency is more than once a day, this is still interpreted per time, e.g. BID for 5 days = 10 repeats.
bridg:DefinedActivity.repeatQuantityRange
urn:CTR_Rr2:First_dose_in_FIH_Total_Dose_Number
bridg:DefinedActivity.repeatQuantityRange
urn:CTR_Rr2:Maximum_dose_Total_Dose_Number
bridg:DefinedActivity.repeatQuantityRange
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatQuantityRange
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatQuantityRange
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatQuantityRange
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:DefinedActivity.repeatQuantityRange
urn:TDM:CyclingRule.repeatCount
bridg:DefinedActivity.statusCode
statusCode
bridg:DefinedActivity.statusCode
false
bridg:DefinedActivity.statusCode
A coded value specifying the phase in the lifecycle of the activity as part of a global library.
bridg:DefinedActivity.statusCode
Draft New
bridg:DefinedActivity.statusCode
Released
bridg:DefinedActivity.statusCode
Retired Archived
bridg:DefinedActivity.statusCode
Please refer to the Defined Activity Status state transition diagram for further details.
bridg:DefinedActivity.statusCode
urn:CTRPv1.0:PlannedEligibilityCriterion.statusCode
bridg:DefinedActivity.statusCode
urn:CTRPv1.0:PlannedObservation.statusCode
bridg:DefinedActivity.statusCode
urn:CTRPv1.0:PlannedActivity.statusCode
bridg:DefinedActivity.statusCode
urn:CTRv1.0:DefinedActivity.statusCode
bridg:DefinedActivity.statusCode
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol//plannedStudy/precondition/eligibilityCriterion.statusCode
bridg:DefinedActivity.statusDate
statusDate
bridg:DefinedActivity.statusDate
false
bridg:DefinedActivity.statusDate
The date (and time) on which the status is assigned to the activity.
bridg:DefinedActivity.statusDate
urn:CTRPv1.0:PlannedObservation.statusDateRange
bridg:DefinedActivity.statusDate
urn:CTRPv1.0:PlannedActivity.statusDateRange
bridg:DefinedActivity.statusDate
urn:CTRPv1.0:PlannedEligibilityCriterion.statusDateRange
bridg:DefinedActivity.statusDate
urn:CTRv1.0:DefinedActivity.statusDate
bridg:DefinedActivity.subcategoryCode
subcategoryCode
bridg:DefinedActivity.subcategoryCode
false
bridg:DefinedActivity.subcategoryCode
A coded value specifying a subdivision within a larger category of activities.
bridg:DefinedActivity.subcategoryCode
chemotherapy
bridg:DefinedActivity.subcategoryCode
radiotherapy
bridg:DefinedActivity.subcategoryCode
hormonal therapy
bridg:DefinedActivity.subcategoryCode
alternative therapy
bridg:DefinedActivity.subcategoryCode
In the case where categoryCode = "anti-cancer treatment"
bridg:DefinedActivity.subcategoryCode
subcategoryCode may = "radiotherapy"
bridg:DefinedActivity.subcategoryCode
and nameCode may = "external beam radiotherapy".
bridg:DefinedActivity.subcategoryCode
If categoryCode = "Intervention"
bridg:DefinedActivity.subcategoryCode
subcategoryCode may = "Drug" (including placebo)
bridg:DefinedActivity.subcategoryCode
"Device" (including sham)
bridg:DefinedActivity.subcategoryCode
"Biological/Vaccine"
bridg:DefinedActivity.subcategoryCode
"Procedure/Surgery"
bridg:DefinedActivity.subcategoryCode
"Radiation"
bridg:DefinedActivity.subcategoryCode
"Behavioral" (e.g.
bridg:DefinedActivity.subcategoryCode
Psychotherapy
bridg:DefinedActivity.subcategoryCode
Lifestyle Counseling)
bridg:DefinedActivity.subcategoryCode
"Genetic" (including gene transfer
bridg:DefinedActivity.subcategoryCode
stem cell and recombinant DNA)
bridg:DefinedActivity.subcategoryCode
Dietary Supplement.
bridg:DefinedActivity.subcategoryCode
Theoretically speaking, the categoryCode should be derivable from the subcategoryCode, however if there may only be a category and not a subcategory, then both attributes must be present in the model.
bridg:DefinedActivity.subcategoryCode
urn:CDASHv1.1:LB.LBSCAT
bridg:DefinedActivity.subcategoryCode
urn:CDASHv1.1:DA.DASCAT
bridg:DefinedActivity.subcategoryCode
urn:CDASHv1.1:MH.MHSCAT
bridg:DefinedActivity.subcategoryCode
urn:CTOM:Surgery.type
bridg:DefinedActivity.subcategoryCode
urn:CTR_Rr2:Specific_paediatric_formulation
bridg:DefinedActivity.subcategoryCode
urn:CTRPv1.0:PlannedActivity.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:CTRPv1.0:PlannedEligibilityCriterion.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:CTRPv1.0:Activity.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:CTRPv1.0:SubstanceAdministration.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:CTRPv1.0:PlannedObservation.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:CTRPv3.8:Activity.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:CTRv1.0:DefinedActivity.subcategoryCode
bridg:DefinedActivity.subcategoryCode
urn:Lab:Activity.typeModifier
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:DA.DASCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:SU.SUSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:IE.IESCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:QS.QSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:PE.PESCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:VS.VSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:CM.CMSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:LB.LBSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:DS.DSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:SC.SCSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:EX.EXSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:MH.MHSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.1:EG.EGSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:SC.SCSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:CM.CMSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:QS.QSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:MS.MSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:EG.EGSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:DS.DSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:PE.PESCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:PP.PPSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:MB.MBSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:VS.VSSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:MH.MHSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:SU.SUSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:LB.LBSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:DS.DSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:DA.DASCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:CE.CESCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:TI.IESCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:FA.FASCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:PC.PCSCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:IE.IESCAT
bridg:DefinedActivity.subcategoryCode
urn:SDTM_IGv3.1.2:EX.EXSCAT
bridg:DefinedAdverseEvent.categoryCode
categoryCode
bridg:DefinedAdverseEvent.categoryCode
false
bridg:DefinedAdverseEvent.categoryCode
A coded value specifying a classification of the adverse event.
bridg:DefinedAdverseEvent.categoryCode
bleeding
bridg:DefinedAdverseEvent.categoryCode
hypoglycemia
bridg:DefinedAdverseEvent.categoryCode
Theoretically speaking, the category should be derivable from the subcategory, however if there may only be a category and not a subcategory, then both attributes must be present in the model.
bridg:DefinedAdverseEvent.categoryCode
urn:CTRv1.0:DefinedAdverseEvent.categoryCode
bridg:DefinedAdverseEvent.categoryCode
urn:SDTM_IGv3.1.2:AE.AECAT
bridg:DefinedAdverseEvent.severityCode
severityCode
bridg:DefinedAdverseEvent.severityCode
false
bridg:DefinedAdverseEvent.severityCode
A coded value specifying the intensity of the event.
bridg:DefinedAdverseEvent.severityCode
Moderate could be used to describe acne.
bridg:DefinedAdverseEvent.severityCode
urn:CTRv1.0:DefinedAdverseEvent.severityCode
bridg:DefinedAdverseEvent.severityCode
urn:SDTM_IGv3.1.2:AE.AESEV
bridg:DefinedAdverseEvent.subcategoryCode
subcategoryCode
bridg:DefinedAdverseEvent.subcategoryCode
false
bridg:DefinedAdverseEvent.subcategoryCode
A coded value specifying a subdivision within a larger category of an adverse event.
bridg:DefinedAdverseEvent.subcategoryCode
neurologic
bridg:DefinedAdverseEvent.subcategoryCode
Theoretically speaking, the category should be derivable from the subcategory, however if there may only be a category and not a subcategory, then both attributes must be present in the model.
bridg:DefinedAdverseEvent.subcategoryCode
urn:CTRv1.0:DefinedAdverseEvent.subcategoryCode
bridg:DefinedAdverseEvent.subcategoryCode
urn:SDTM_IGv3.1.2:AE.AESCAT
bridg:DefinedCompositionRelationship.joinCode
joinCode
bridg:DefinedCompositionRelationship.joinCode
false
bridg:DefinedCompositionRelationship.joinCode
A coded value specifying whether, and how, a specific activity in a set of parallel activities should come together before subsequent activities can begin.
bridg:DefinedCompositionRelationship.joinCode
Wait for this activity to complete before the subsequent activity; Terminate this activity as soon as all parallel "wait" activities are completed (and if this activity hasn't started yet
bridg:DefinedCompositionRelationship.joinCode
don't start it at all); Continue this activity after all "wait" activities complete
bridg:DefinedCompositionRelationship.joinCode
but don't wait for it to complete before beginning subsequent activities.
bridg:DefinedCompositionRelationship.joinCode
urn:CTRv1.0:DefinedCompositionRelationship.joinCode
bridg:DefinedCompositionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:DefinedCompositionRelationship.pauseQuantityRange
false
bridg:DefinedCompositionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:DefinedCompositionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:DefinedCompositionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:DefinedCompositionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:DefinedCompositionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
New content
bridg:DefinedCompositionRelationship.pauseQuantityRange
urn:TDMv2:
bridg:DefinedCompositionRelationship.sequenceNumber
sequenceNumber
bridg:DefinedCompositionRelationship.sequenceNumber
false
bridg:DefinedCompositionRelationship.sequenceNumber
An integer specifying the relative sequential or temporal ordering of this relationship among other similar relationships having the same source.
bridg:DefinedCompositionRelationship.sequenceNumber
In a course of treatment (a composite activity) that is composed of a chemotherapy activity and a radiotherapy activity, the sequence number indicates which component activity precedes the other.
bridg:DefinedCompositionRelationship.sequenceNumber
urn:C3PR:EligibilityCriterion.questionNumber
bridg:DefinedCompositionRelationship.sequenceNumber
urn:C3PRv2.9:EligibilityCriteria.questionNumber
bridg:DefinedCompositionRelationship.sequenceNumber
urn:CTOM:ActivityRelationship.sequenceNumber
bridg:DefinedCompositionRelationship.sequenceNumber
urn:CTRv1.0:DefinedCompositionRelationship.sequenceNumber
bridg:DefinedContingentOnRelationship.checkpointCode
checkpointCode
bridg:DefinedContingentOnRelationship.checkpointCode
false
bridg:DefinedContingentOnRelationship.checkpointCode
bridg:DefinedContingentOnRelationship.checkpointCode
The checkpointCode specifies when the precondition is to be checked; it is analogous to the various conditional statements and loop constructs in programming languages "while-do" vs. "do-while" or "repeat-until" vs. "loop-exit."
bridg:DefinedContingentOnRelationship.checkpointCode
urn:HL7SDr1:Precondition3.checkpointCode
bridg:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
completionRequiredBeforeStartingIndicator
bridg:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
false
bridg:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
Specifies whether the target activity must have completed prior to starting the source activity.
bridg:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
This attribute may only be used if the target is an activity, not if the target is an observation result or a criterion group.
bridg:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
urn:CTRv1.0:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
bridg:DefinedContingentOnRelationship.completionRequiredBeforeStartingIndicator
urn:TDM:TriggeringRule
bridg:DefinedContingentOnRelationship.pauseQuantityRange
pauseQuantityRange
bridg:DefinedContingentOnRelationship.pauseQuantityRange
false
bridg:DefinedContingentOnRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:DefinedContingentOnRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:DefinedContingentOnRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:DefinedContingentOnRelationship.pauseQuantityRange
For the more complex examples of doing activity A 5 minutes after the start of B or 5 minutes after the end of B
bridg:DefinedContingentOnRelationship.pauseQuantityRange
use pauseQuantity in combination with completionRequiredBeforeStartingIndicator where the pauseQuantity in both cases would be 5 minutes and "after the start of" would be completionRequiredBeforeStartingIndicator = "false" and "after the end of" = "true".
bridg:DefinedContingentOnRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:DefinedContingentOnRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:DefinedContingentOnRelationship.priorityNumber
priorityNumber
bridg:DefinedContingentOnRelationship.priorityNumber
false
bridg:DefinedContingentOnRelationship.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:DefinedContingentOnRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:DefinedContingentOnRelationship.priorityNumber
urn:HL7SDr1:Precondition3.priorityNumber
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
joinCode
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
false
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
A coded value specifying whether, and how, a specific activity in a set of parallel activities should come together before subsequent activities can begin.
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
Wait for this activity to complete before the subsequent activity; Terminate this activity as soon as all parallel "wait" activities are completed (and if this activity hasn't started yet
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
don't start it at all); Continue this activity after all "wait" activities complete
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
but don't wait for it to complete before beginning subsequent activities.
bridg:DefinedCriterionGroupCompositionRelationship.joinCode
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship.joinCode
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
false
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
New content
bridg:DefinedCriterionGroupCompositionRelationship.pauseQuantityRange
urn:TDMv2:
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
sequenceNumber
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
false
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
An integer specifying the relative sequential or temporal ordering of this relationship among other similar relationships having the same source.
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
In a criterion group that is composed of a substance administration activity and a lab test activity
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
the sequence number indicates which activity precedes the other.
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
urn:CTOM:ActivityRelationship.sequenceNumber
bridg:DefinedCriterionGroupCompositionRelationship.sequenceNumber
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship.sequenceNumber
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
false
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:DefinedCriterionGroupOptionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:DefinedCriterionGroupOptionRelationship.priorityNumber
priorityNumber
bridg:DefinedCriterionGroupOptionRelationship.priorityNumber
false
bridg:DefinedCriterionGroupOptionRelationship.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:DefinedCriterionGroupOptionRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:DefinedCriterionGroupOptionRelationship.priorityNumber
urn:CTRv1.0:DefinedCriterionGroupOptionRelationship.priorityNumber
bridg:DefinedCriterionGroupOptionRelationship.priorityNumber
urn:TDM:AbstractRule.isExclusive
bridg:DefinedEligibilityCriterion.requiredResponse
requiredResponse
bridg:DefinedEligibilityCriterion.requiredResponse
false
bridg:DefinedEligibilityCriterion.requiredResponse
The reply necessary to include/exclude a potential subject on a study.
bridg:DefinedEligibilityCriterion.requiredResponse
urn:CTRv1.0:DefinedEligibilityCriterion.requiredResponse
bridg:DefinedEligibilityCriterionAnswer.requiredIndicator
requiredIndicator
bridg:DefinedEligibilityCriterionAnswer.requiredIndicator
false
bridg:DefinedEligibilityCriterionAnswer.requiredIndicator
Specifies whether this reply is necessary to include/exclude a potential subject on a study.
bridg:DefinedEligibilityCriterionAnswer.requiredIndicator
This attribute is only intended to be used when the required answer is defined in the context of the question, regardless of in which study it is used.
bridg:DefinedEligibilityCriterionAnswer.requiredIndicator
urn:BRIDGSCC:Model_Integrity
bridg:DefinedExperimentalUnitAllocation.methodCode
methodCode
bridg:DefinedExperimentalUnitAllocation.methodCode
false
bridg:DefinedExperimentalUnitAllocation.methodCode
A coded value specifying the technique that is used for allocating experimental units.
bridg:DefinedExperimentalUnitAllocation.methodCode
adaptive
bridg:DefinedExperimentalUnitAllocation.methodCode
blocked
bridg:DefinedExperimentalUnitAllocation.methodCode
stratified
bridg:DefinedExperimentalUnitAllocation.methodCode
allocation based on past response.
bridg:DefinedExperimentalUnitAllocation.methodCode
urn:BRIDGv2.2:ExperimentalUnitAllocationMethod.typeCode
bridg:DefinedExperimentalUnitAllocation.methodCode
urn:CTRv1.0:DefinedExperimentalUnitAllocation.methodCode
bridg:DefinedExpressionVariableRelationship.localVariableName
localVariableName
bridg:DefinedExpressionVariableRelationship.localVariableName
false
bridg:DefinedExpressionVariableRelationship.localVariableName
A label that represents the result value of an observation and serves as an input parameter used in a dose expression.
bridg:DefinedExpressionVariableRelationship.localVariableName
The local variable name is used in the DefinedSubstanceAdministration.dose.EXPR<PQ> and will ultimately be substituted with the result of the observation to which the DefinedExpressionVariableRelationship points.
bridg:DefinedExpressionVariableRelationship.localVariableName
urn:BRIDGSCC:Model_Integrity
bridg:DefinedExpressionVariableRelationship.localVariableName
urn:CTRv1.0:DefinedExpressionVariableRelationship.localVariableName
bridg:DefinedImaging.contrastAgentEnhancementIndicator
contrastAgentEnhancementIndicator
bridg:DefinedImaging.contrastAgentEnhancementIndicator
false
bridg:DefinedImaging.contrastAgentEnhancementIndicator
Specifies whether the image is enhanced by the use of a contrast agent.
bridg:DefinedImaging.contrastAgentEnhancementIndicator
urn:CTOM:Imaging.contrastAgentEnhancementIndicator
bridg:DefinedImaging.contrastAgentEnhancementIndicator
urn:CTRv1.0:DefinedImaging.contrastAgentEnhancementIndicator
bridg:DefinedImaging.enhancementDescription
enhancementDescription
bridg:DefinedImaging.enhancementDescription
false
bridg:DefinedImaging.enhancementDescription
The textual representation for how an image is enhanced either physically or electronically.
bridg:DefinedImaging.enhancementDescription
urn:CTOM:Imaging.enhancementDescriptionText
bridg:DefinedImaging.enhancementDescription
urn:CTRv1.0:DefinedImaging.enhancementDescription
bridg:DefinedImaging.enhancementRate
enhancementRate
bridg:DefinedImaging.enhancementRate
false
bridg:DefinedImaging.enhancementRate
The numeric value to indicate an increase in voxel signal over time for an MRI, expressed as signal intensity units per second.
bridg:DefinedImaging.enhancementRate
urn:CTOM:Imaging.enhancementRateValue
bridg:DefinedNotification.deliveryMechanismCode
deliveryMechanismCode
bridg:DefinedNotification.deliveryMechanismCode
false
bridg:DefinedNotification.deliveryMechanismCode
A coded value specifying how the notification message is to be delivered.
bridg:DefinedNotification.deliveryMechanismCode
email
bridg:DefinedNotification.deliveryMechanismCode
urn:C3PRv2.9:PlannedNotification.deliveryMechanism
bridg:DefinedNotification.message
message
bridg:DefinedNotification.message
false
bridg:DefinedNotification.message
The text that is to be included in the notification.
bridg:DefinedNotification.message
The message text may contain substitution tags that when used in the context of a particular study are replaced with study name or study site, etc.
bridg:DefinedNotification.message
urn:C3PRv2.9:PlannedNotification.message
bridg:DefinedNotification.messageTitle
messageTitle
bridg:DefinedNotification.messageTitle
false
bridg:DefinedNotification.messageTitle
The topic of the notification.
bridg:DefinedNotification.messageTitle
urn:C3PRv2.9:PlannedNotification.title
bridg:DefinedNotification.messageTitle
urn:caAERSv2.2:PlannedEmailNotification.subjectLine
bridg:DefinedObservation.approachAnatomicSiteCode
approachAnatomicSiteCode
bridg:DefinedObservation.approachAnatomicSiteCode
false
bridg:DefinedObservation.approachAnatomicSiteCode
A coded value specifying the anatomic location or access point for an observation.
bridg:DefinedObservation.approachAnatomicSiteCode
Anus for a colonoscopy observation
bridg:DefinedObservation.approachAnatomicSiteCode
Neither target anatomic site nor approach anatomic site is necessarily required or relevant for certain observations, however if either or both are present then the distinction between them is that the approach site is the acces point for the measurement or observation and the target site is what is ultimately being evaluated.
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code
structure or as multiple code repetitions.
bridg:DefinedObservation.approachAnatomicSiteCode
urn:CDASHv1.1:VS.VSLOC
bridg:DefinedObservation.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:FA.FALOC
bridg:DefinedObservation.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:EG.EGLOC
bridg:DefinedObservation.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:VS.VSLOC
bridg:DefinedObservation.bodyPositionCode
bodyPositionCode
bridg:DefinedObservation.bodyPositionCode
false
bridg:DefinedObservation.bodyPositionCode
A coded value specifying the 3-dimensional spatial orientation of a subject during a particular observation.
bridg:DefinedObservation.bodyPositionCode
supine
bridg:DefinedObservation.bodyPositionCode
trendelenburg
bridg:DefinedObservation.bodyPositionCode
standing
bridg:DefinedObservation.bodyPositionCode
urn:CTOM:ClinicalResult.bodyPositionCode
bridg:DefinedObservation.bodyPositionCode
urn:CTRv1.0:DefinedObservation.bodyPositionCode
bridg:DefinedObservation.bodyPositionCode
urn:PSC:VS.VSPOS
bridg:DefinedObservation.bodyPositionCode
urn:SDTM_IGv3.1.1:EG.EGPOS
bridg:DefinedObservation.focalDateRange
focalDateRange
bridg:DefinedObservation.focalDateRange
false
bridg:DefinedObservation.focalDateRange
The time period in which the observation result is held to be true, expressed either as a simple date range or as an evaluable expression that references a study-defined date or milestone.
bridg:DefinedObservation.focalDateRange
For a survey question
bridg:DefinedObservation.focalDateRange
"Have you traveled to Europe between 1990 and 1999?"
bridg:DefinedObservation.focalDateRange
the focalDateRange would be "January 1
bridg:DefinedObservation.focalDateRange
1990 to December 31
bridg:DefinedObservation.focalDateRange
1999".
bridg:DefinedObservation.focalDateRange
For the question
bridg:DefinedObservation.focalDateRange
"Have you smoked in the last 2 months"
bridg:DefinedObservation.focalDateRange
the focalDateRange would be an expression referencing a variable that represents the PerformedObservation.actualDateRange (a value yet to be defined) and a formula for the date range between when the question is asked (PerformedObservation.actualDateRange.low) and 2 months prior (PerformedObservation.actualDateRange.low - 2 months).
bridg:DefinedObservation.focalDateRange
As an attribute with data type IVL<EXPR<TS.DATETIME>>, focalDateRange can be used to express a simple date range such as "January 1, 1990 to December 31, 1999" or a relative time expression that includes a variable that represents another date in the model that is a study-defined anchor point. The other date may or may not be known at the time the DefinedObservation is created, but will be known by the time the PerformedObservation is created.
bridg:DefinedObservation.focalDateRange
urn:CTOM:Histopathology.reportingDate
bridg:DefinedObservation.focalDateRange
urn:CTOM:DiseaseResponse.evaluationDate
bridg:DefinedObservation.focalDateRange
urn:CTOM:DiseaseResponse.progressionDate
bridg:DefinedObservation.focalDateRange
urn:CTOM:Diagnosis.confirmationDate
bridg:DefinedObservation.focalDateRange
urn:CTRv1.0:DefinedObservation.focalDateRange
bridg:DefinedObservation.focalDateRange
urn:SDTM_IGv3.1.2:QS.QSEVLINT
bridg:DefinedObservation.focalDuration
focalDuration
bridg:DefinedObservation.focalDuration
true
bridg:DefinedObservation.focalDuration
A quantity of time in which the observation result is held to be true.
bridg:DefinedObservation.focalDuration
2 months is the focalDuration for the question
bridg:DefinedObservation.focalDuration
"Have you smoked in the last 2 months?"
bridg:DefinedObservation.focalDuration
The focalDuration can be derived from the expression captured in the focalDateRange.IVL<EXPR<TS.DATETIME>>.
bridg:DefinedObservation.focalDuration
urn:CTOM:DiseaseResponse.progressionPeriodUnitOfMeasureCode
bridg:DefinedObservation.focalDuration
urn:CTOM:DiseaseResponse.progressionPeriod
bridg:DefinedObservation.focalDuration
urn:CTRv1.0:DefinedObservation.focalDuration
bridg:DefinedObservation.focalDuration
urn:SDTM_IGv3.1.1:QS.QSEVLINT
bridg:DefinedObservation.methodCode
methodCode
bridg:DefinedObservation.methodCode
false
bridg:DefinedObservation.methodCode
A coded value specifying the technique that is used for the observation.
bridg:DefinedObservation.methodCode
Arterial puncture
bridg:DefinedObservation.methodCode
sphygmomanometry (for blood pressure measurement)
bridg:DefinedObservation.methodCode
Global introspection
bridg:DefinedObservation.methodCode
algorithm
bridg:DefinedObservation.methodCode
bayesian (for Adverse Event causality)
bridg:DefinedObservation.methodCode
Estrogen Receptor Assay
bridg:DefinedObservation.methodCode
Progesterone Receptor Assay
bridg:DefinedObservation.methodCode
p53 Assay (for clinical result assay)
bridg:DefinedObservation.methodCode
urn:AE:CausalAssessment.methodCode
bridg:DefinedObservation.methodCode
urn:AE:PerformedProductInvestigation.evaluationMethodCode
bridg:DefinedObservation.methodCode
urn:CTOM:ClinicalResult.labTechniqueCode
bridg:DefinedObservation.methodCode
urn:CTOM:LesionDescription.methodCode
bridg:DefinedObservation.methodCode
urn:CTOM:ClinicalResult.meansVitalStatusObtainedCode
bridg:DefinedObservation.methodCode
urn:CTOM:ClinicalResult.assayMethodCode
bridg:DefinedObservation.methodCode
urn:CTRv1.0:DefinedObservation.methodCode
bridg:DefinedObservation.methodCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Observation.methodCode
bridg:DefinedObservation.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:DefinedObservation.targetAnatomicSiteCode
false
bridg:DefinedObservation.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of the observation.
bridg:DefinedObservation.targetAnatomicSiteCode
lung
bridg:DefinedObservation.targetAnatomicSiteCode
leg
bridg:DefinedObservation.targetAnatomicSiteCode
The target site of the observation result may be different than the target site of the observation that generated it. For instance, the target site of the observation may be broad (e.g. skin) while the target site of the observation result is specific (e.g. skin on chest).
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:DefinedObservation.targetAnatomicSiteCode
urn:AE:AdverseEvent.bodyLocation
bridg:DefinedObservation.targetAnatomicSiteCode
urn:CTOM:Diagnosis.primaryAnatomicSiteLateralityCode
bridg:DefinedObservation.targetAnatomicSiteCode
urn:CTOM:LesionDescription.anatomicSiteCode
bridg:DefinedObservation.targetAnatomicSiteCode
urn:CTOM:Diagnosis.primaryAnatomicSiteCode
bridg:DefinedObservation.targetAnatomicSiteCode
urn:CTOM:Diagnosis.primaryAnatomicSiteCodeSystem
bridg:DefinedObservation.targetAnatomicSiteCode
urn:CTOM:LesionDescription.anatomicSiteCodeSystem
bridg:DefinedObservation.targetAnatomicSiteCode
urn:CTRv1.0:DefinedObservation.targetAnatomicSiteCode
bridg:DefinedObservation.targetAnatomicSiteCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Observation.TargetSiteCode
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
false
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for an observation.
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
bilateral
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
left
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
right
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
urn:AE:AdverseEvent.bodyLocation
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
urn:CTOM:Diagnosis.primaryAnatomicSiteLateralityCode
bridg:DefinedObservation.targetAnatomicSiteLateralityCode
urn:CTRv1.0:DefinedObservation.targetAnatomicSiteLateralityCode
bridg:DefinedObservationResult.comment
comment
bridg:DefinedObservationResult.comment
false
bridg:DefinedObservationResult.comment
Additional description of the observation result.
bridg:DefinedObservationResult.comment
urn:CTOM:DiseaseResponse.commentText
bridg:DefinedObservationResult.comment
urn:CTRv1.0:DefinedObservationResult.comment
bridg:DefinedObservationResult.comment
urn:Lab:LabResult.referenceRangeComments
bridg:DefinedObservationResult.comment
urn:SDTM_IGv3.1.1:CO.COVAL
bridg:DefinedObservationResult.confidentialityCode
confidentialityCode
bridg:DefinedObservationResult.confidentialityCode
false
bridg:DefinedObservationResult.confidentialityCode
A coded value specifying the degree of privacy applicable for the observation result.
bridg:DefinedObservationResult.confidentialityCode
urn:CTOM:Histopathology.confidentialityCode
bridg:DefinedObservationResult.confidentialityCode
urn:CTOM:LesionDescription.confidentialityCode
bridg:DefinedObservationResult.confidentialityCode
urn:CTOM:Observation.confidentialityCode
bridg:DefinedObservationResult.confidentialityCode
urn:CTOM:ClinicalResult.confidentialityCode
bridg:DefinedObservationResult.confidentialityCode
urn:CTRv1.0:DefinedObservationResult.confidentialityCode
bridg:DefinedObservationResult.derivationExpression
derivationExpression
bridg:DefinedObservationResult.derivationExpression
false
bridg:DefinedObservationResult.derivationExpression
A character string containing a formal language expression that specifies how the observation result's attributes are, should be, or have been derived from input parameters associated with activity.
bridg:DefinedObservationResult.derivationExpression
urn:CTRv1.0:DefinedObservationResult.derivationExpression
New content
bridg:DefinedObservationResult.derivationExpression
urn:TDMv2:
bridg:DefinedObservationResult.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:DefinedObservationResult.targetAnatomicSiteCode
false
bridg:DefinedObservationResult.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of an observation result.
bridg:DefinedObservationResult.targetAnatomicSiteCode
Arm for skin rash.
bridg:DefinedObservationResult.targetAnatomicSiteCode
The target site of the observation result may be different than the target site of the observation that generated it. For instance, the target site of the observation may be broad (e.g. skin) while the target site of the observation result is specific (e.g. skin on chest).
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:CTOM:LesionDescription.contactAnatomicSiteCodeSystem
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:CTOM:LesionDescription.contactAnatomicSiteCode
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:CTRv1.0:DefinedObservationResult.targetAnatomicSiteCode
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:DefinedObservationResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
false
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for a procedure.
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
bilateral
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
left
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
right
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
urn:CTRv1.0:DefinedObservationResult.targetAnatomicSiteLateralityCode
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:DefinedObservationResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:DefinedObservationResult.targetCodingSystem
targetCodingSystem
bridg:DefinedObservationResult.targetCodingSystem
false
bridg:DefinedObservationResult.targetCodingSystem
The coding system to use for recording results for the associated activity or evaluation.
bridg:DefinedObservationResult.targetCodingSystem
urn:BRIDGv2.2:PlannedObservationResult.targetCodingSystem
bridg:DefinedObservationResult.targetCodingSystem
urn:CTRv1.0:DefinedObservationResult.targetCodingSystem
bridg:DefinedObservationResult.typeCode
typeCode
bridg:DefinedObservationResult.typeCode
false
bridg:DefinedObservationResult.typeCode
A coded value specifying the kind of observation result.
bridg:DefinedObservationResult.typeCode
For blood pressure
bridg:DefinedObservationResult.typeCode
the results might be 120 for systolic and 80 for diastolic
bridg:DefinedObservationResult.typeCode
where systolic and diastolic are the typeCode distinguishing the two numbers.
bridg:DefinedObservationResult.typeCode
urn:CTOM:ClinicalResult.value
bridg:DefinedObservationResult.typeCode
urn:CTRRr3:DefinedObservationResult.typeCode
bridg:DefinedObservationResult.typeCode
urn:CTRv1.0:DefinedObservationResult.typeCode
bridg:DefinedObservationResult.value
value
bridg:DefinedObservationResult.value
false
bridg:DefinedObservationResult.value
Data or information that is determined by an act of observation.
bridg:DefinedObservationResult.value
The result of a lab test
bridg:DefinedObservationResult.value
physical finding
bridg:DefinedObservationResult.value
self-reported symptom.
bridg:DefinedObservationResult.value
The adverse event term code.
bridg:DefinedObservationResult.value
The DefinedObservationResult class can be used to represent defined ranges for contingencies by constraining the result attribute from ANY to IVL<PQ>, for instance, or any other range value. Such DefinedObservationResults may be used as criteria for conditional activities or repeated activities.
bridg:DefinedObservationResult.value
urn:AE:AdverseEvent.adverseEventTermCode
bridg:DefinedObservationResult.value
urn:AE:Animal.overallStateOfHealthCode
bridg:DefinedObservationResult.value
urn:AE:AdverseEvent.reactionText
bridg:DefinedObservationResult.value
urn:AE:Person.numberOfSiblings
bridg:DefinedObservationResult.value
urn:AE:InvestigativeSubject.gestationPeriod
bridg:DefinedObservationResult.value
urn:AE:ProductInvestigation.evaluationResultCode
bridg:DefinedObservationResult.value
urn:AE:Assessment.textInterpretation
bridg:DefinedObservationResult.value
urn:AE:Assessment.codedInterpretation
bridg:DefinedObservationResult.value
urn:AE:ProductObservation.value
bridg:DefinedObservationResult.value
urn:C3PR:StratificationCriterionPermissbleAnswer.permissibleAnswer
bridg:DefinedObservationResult.value
urn:C3PRv2.9:StratificationCriterionPermissibleAnswer.permissibleAnswer
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.survivalStatusCode
bridg:DefinedObservationResult.value
urn:CTOM:DiseaseResponse.courseDispositionCode
bridg:DefinedObservationResult.value
urn:CTOM:DiseaseResponse.responseCode
bridg:DefinedObservationResult.value
urn:CTOM:LesionEvaluation.evaluationCode
bridg:DefinedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.abortionIndicator
bridg:DefinedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.stillBirthCount
bridg:DefinedObservationResult.value
urn:CTOM:ClinicalResult.valueUnitOfMeasureCode
bridg:DefinedObservationResult.value
urn:CTOM:ClinicalResult.value
bridg:DefinedObservationResult.value
urn:CTOM:Diagnosis.diseaseDiagnosisCodeSystem
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.painIndexCodeSystem
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.anamResultAccuracyPercent
bridg:DefinedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.firstLiveBirthAge
bridg:DefinedObservationResult.value
urn:CTOM:Diagnosis.diseaseStatusCode
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.performanceStatusCode
bridg:DefinedObservationResult.value
urn:CTOM:Participant.householdIncomeCode
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.menstrualIndicator
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.menstrualPatternTypeCode
bridg:DefinedObservationResult.value
urn:CTOM:CancerStage.stageCode
bridg:DefinedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.menopauseAge
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.performanceStatusCodeSystem
bridg:DefinedObservationResult.value
urn:CTOM:DeathSummary.deathCauseCode
bridg:DefinedObservationResult.value
urn:CTOM:Diagnosis.diseaseDiagnosisCode
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.survivalStatusDescriptionText
bridg:DefinedObservationResult.value
urn:CTOM:DeathSummary.deathCauseText
bridg:DefinedObservationResult.value
urn:CTOM:AdverseEvent.descriptionText
bridg:DefinedObservationResult.value
urn:CTOM:PartcipantEligibilityAnswer.answerText
bridg:DefinedObservationResult.value
urn:CTOM:CancerStage.stageCodeSystem
bridg:DefinedObservationResult.value
urn:CTOM:Histopathology.grossExamResultCode
bridg:DefinedObservationResult.value
urn:CTOM:Diagnosis.recurrenceIndicator
bridg:DefinedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.liveBirthCount
bridg:DefinedObservationResult.value
urn:CTOM:DiseaseResponse.responseCodeSystem
bridg:DefinedObservationResult.value
urn:CTOM:Specimen.volume
bridg:DefinedObservationResult.value
urn:CTOM:QualitativeEvaluation.painIndexCode
bridg:DefinedObservationResult.value
urn:CTOM:AdverseEvent.outcomeCode
bridg:DefinedObservationResult.value
urn:CTRPv1.0:PlannedEligibilityCriterion.requiredResponse
bridg:DefinedObservationResult.value
urn:CTRPv3.8:PlannedEligibilityCriterion.eligibleGenderCode
bridg:DefinedObservationResult.value
urn:CTRPv3.8:PlannedEligibilityCriterion.value
bridg:DefinedObservationResult.value
urn:CTRPv3.8:PlannedEligibilityCriterion.textValue
bridg:DefinedObservationResult.value
urn:CTRR:Past_Population_Disease_Condition
e.g. informed consent
bridg:DefinedObservationResult.value
urn:CTRR:Ethical_Considerations
bridg:DefinedObservationResult.value
urn:CTRR:BMI
bridg:DefinedObservationResult.value
urn:CTRR:Special_Populations
bridg:DefinedObservationResult.value
urn:CTRR:Maximum_Age
bridg:DefinedObservationResult.value
urn:CTRR:Gestational_Age
bridg:DefinedObservationResult.value
urn:CTRR:Substance_Use
s
bridg:DefinedObservationResult.value
urn:CTRR:Subject_Race
bridg:DefinedObservationResult.value
urn:CTRR:Lifestyle_Choices
bridg:DefinedObservationResult.value
urn:CTRR:Current_Population_Disease_Condition
s
bridg:DefinedObservationResult.value
urn:CTRR:Prior_and_Concomitant_Medication
bridg:DefinedObservationResult.value
urn:CTRR:Nursing
bridg:DefinedObservationResult.value
urn:CTRR:Subject_Ethnicity
bridg:DefinedObservationResult.value
urn:CTRR:Subject_Gender
bridg:DefinedObservationResult.value
urn:CTRR:Minimum_Age
bridg:DefinedObservationResult.value
urn:CTRR:Pregnancy
bridg:DefinedObservationResult.value
urn:CTRRr3:DefinedObservationResult.result
bridg:DefinedObservationResult.value
urn:CTRv1.0:DefinedObservationResult.value
bridg:DefinedObservationResult.value
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol//plannedStudy/precondition/eligibilityCriterion.value
bridg:DefinedObservationResult.value
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Observation.value
bridg:DefinedObservationResult.value
urn:HL7SP:VerificationEvent.value
bridg:DefinedObservationResult.value
urn:Lab:LabResult.textResult
bridg:DefinedObservationResult.value
urn:Lab:LabResult.referenceTextList
bridg:DefinedObservationResult.value
urn:Lab:LabResult.numericResult
bridg:DefinedObservationResult.value
urn:Lab:LabResult.numericPrecision
bridg:DefinedObservationResult.value
urn:PSCv2.6:PlannedActivity.condition
bridg:DefinedObservationResult.value
urn:PSCv2.6:ScheduledActivity.condition
bridg:DefinedObservationResult.value
urn:PSCv2.6:Population.name
bridg:DefinedObservationResult.value
urn:PSCv2.6:Population.abbreviation
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:TS.TSVAL
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSORRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PESTRESN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PESTRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PEORRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:IE.IESTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:DV.DVDECOD
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBLOINC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGSTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGORRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:DS.DSTERM
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSSTRESN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PEORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:CM.CMOCCUR
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBSTRESN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSORRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCSTRESN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:MH.MHOCCUR
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:MH.MHTERM
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSSTRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGSTRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSLOINC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCORRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBSTRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:MH.MHDECOD
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:IE.IEORRES
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGLOINC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSSTRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCSTRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSSTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSSTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PESTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGSTRESN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCSTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBORRESU
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBSTRESC
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSSTRESN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARM_where_TSPARMCD_TDIGRP
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARMCD_where_TSPARMCD_SEXPOP
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARMCD_where_TSPARMCD_TDIGRP
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_AGEMAX
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARM_where_TSPARMCD_AGEMIN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_TDIGRP
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARMCD_where_TSPARMCD_AGEMIN
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARM_where_TSPARMCD_AGEMAX
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARM_where_TSPARMCD_SEXPOP
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSPARMCD_where_TSPARMCD_AGEMAX
bridg:DefinedObservationResult.value
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_SEXPOP
bridg:DefinedObservationResult.value
urn:caAERSv2.2:Ctc.name___SolicitedAdverseEvent
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___ExpectedAECtcTerm
otherTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:MeddraVersion.name___SolicitedAdverseEvent
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.version_id
bridg:DefinedObservationResult.value
urn:caAERSv2.2:CtcTerm.ctepCode___AbstractExpectedAE
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.meddraTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.costartSymbol
meddraTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:MeddraVersion.name___SolicitedAdverseEvent
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.icd9CmCode
bridg:DefinedObservationResult.value
urn:caAERSv2.2:MeddraVersion.name___ExpectedAEMeddraLowLevelTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:MeddraVersion.name___ExpectedAECtcTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:CtcTerm.select___AbstractExpectedAE
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.whoArtCode
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___ExpectedAEMeddraLowLevelTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.icd10Code
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.jartCode
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.hartsCode
bridg:DefinedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.icd9Code
bridg:DefinedObservationResult.value
urn:caAERSv2.2:Ctc.name___ExpectedAECtcTerm
bridg:DefinedObservationResult.value
urn:caAERSv2.2:CtcTerm.term___AbstractExpectedAE
bridg:DefinedObservationResult.valueNegationIndicator
valueNegationIndicator
bridg:DefinedObservationResult.valueNegationIndicator
false
bridg:DefinedObservationResult.valueNegationIndicator
Specifies whether, when the observation event occurred, the finding communicated by the value attribute was NOT found.
bridg:DefinedObservationResult.valueNegationIndicator
This attribute should only be used when the terminology used for DefinedObservationResult.value is not itself capable of expressing negated findings (e.g., ICD9).
bridg:DefinedObservationResult.valueNegationIndicator
urn:HL7SDr1:TimePointEventDefinition.negationInd
bridg:DefinedOptionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:DefinedOptionRelationship.pauseQuantityRange
false
bridg:DefinedOptionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:DefinedOptionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:DefinedOptionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:DefinedOptionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:DefinedOptionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:DefinedOptionRelationship.priorityNumber
priorityNumber
bridg:DefinedOptionRelationship.priorityNumber
false
bridg:DefinedOptionRelationship.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:DefinedOptionRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:DefinedOptionRelationship.priorityNumber
urn:CTRv1.0:DefinedOptionRelationship.priorityNumber
bridg:DefinedOptionRelationship.priorityNumber
urn:TDM:AbstractRule.isExclusive
bridg:DefinedProcedure.approachAnatomicSiteCode
approachAnatomicSiteCode
bridg:DefinedProcedure.approachAnatomicSiteCode
false
bridg:DefinedProcedure.approachAnatomicSiteCode
A coded value specifying the anatomic location or access point for a procedure.
bridg:DefinedProcedure.approachAnatomicSiteCode
Arm for an injection
bridg:DefinedProcedure.approachAnatomicSiteCode
Trans-abdominal for a nephrectomy
bridg:DefinedProcedure.approachAnatomicSiteCode
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:BRIDGv2.2:PlannedProcedure.approachSiteCode
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:CTRv1.0:DefinedProcedure.approachAnatomicSiteCode
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.approachSiteCode
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Procedure.approachSiteCode
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:DefinedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
approachAnatomicSiteLateralityCode
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
false
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is an access point for a procedure.
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
bilateral
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
left
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
right
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
urn:CTRv1.0:DefinedProcedure.approachAnatomicSiteLateralityCode
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:DefinedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:DefinedProcedure.methodCode
methodCode
bridg:DefinedProcedure.methodCode
false
bridg:DefinedProcedure.methodCode
A coded value specifying the technique that is used for the procedure.
bridg:DefinedProcedure.methodCode
For a specimen collection
bridg:DefinedProcedure.methodCode
the methodCode could = "finger stick"
bridg:DefinedProcedure.methodCode
"veni puncture"
bridg:DefinedProcedure.methodCode
"Abdominal/ ascites effusion"
bridg:DefinedProcedure.methodCode
"Biopsy"
bridg:DefinedProcedure.methodCode
"Bronchial alveolar lavage (BAL)".
bridg:DefinedProcedure.methodCode
For a cholecystectomy
bridg:DefinedProcedure.methodCode
the methodCode could = "open"
bridg:DefinedProcedure.methodCode
"laproscopic".
bridg:DefinedProcedure.methodCode
urn:BRIDGv2.2:PlannedProcedure.methodCode
bridg:DefinedProcedure.methodCode
urn:CTRPv3.8:PlannedProcedure.methodCode
bridg:DefinedProcedure.methodCode
urn:CTRv1.0:DefinedProcedure.methodCode
bridg:DefinedProcedure.methodCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Procedure.methodCode
bridg:DefinedProcedure.methodCode
urn:HCTv1.0:CDE_2774532:Techniques.Specify_the_other_erythrocyte_reduced_methods
bridg:DefinedProcedure.methodCode
urn:HCTv1.0:CDE_2750679:Graft_Manipulation.What_was_the_method_of_ex_vivo_graft_manipulation_other_than_for_RBC_removal_or_volume_reduction?
bridg:DefinedProcedure.methodCode
urn:HCTv1.0:CDE_2774742:Techniques.Specify_the_other_T-cell_depletion_method:
bridg:DefinedProcedure.methodCode
urn:HCTv1.0:CDE_2748795:Therapies.What_malignant_cell_removal_method_was_used_to_treat_the_product?
bridg:DefinedProcedure.methodCode
urn:HCTv1.0:CDE_2750692:Graft_Manipulation.Specify_the_ex_vivo_graft_manipulation_other_than_for_RBC_removal_or_volume_reduction:
bridg:DefinedProcedure.nameCodeModifiedText
nameCodeModifiedText
bridg:DefinedProcedure.nameCodeModifiedText
false
bridg:DefinedProcedure.nameCodeModifiedText
A character string that is a revision of the original text of the procedure to enable the coding of the text.
bridg:DefinedProcedure.nameCodeModifiedText
If the original text is "message"
bridg:DefinedProcedure.nameCodeModifiedText
the nameCodeModifiedText could be set to "massage"
bridg:DefinedProcedure.nameCodeModifiedText
so that the text can be successfully coded.
bridg:DefinedProcedure.nameCodeModifiedText
In the context of BRIDG, text modification occurs a single time for a given instance of originalText.
bridg:DefinedProcedure.nameCodeModifiedText
urn:BRIDGSCC:Model_Integrity
bridg:DefinedProcedure.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:DefinedProcedure.targetAnatomicSiteCode
false
bridg:DefinedProcedure.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of a procedure.
bridg:DefinedProcedure.targetAnatomicSiteCode
Kidney for a nephrectomy
bridg:DefinedProcedure.targetAnatomicSiteCode
Multiple contiguous sites within the same organ system may be referenced.
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:BRIDGv2.2:PlannedProcedure.targetSiteCode
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:CTRPv3.8:PlannedProcedure.targetSiteCode
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:CTRv1.0:DefinedProcedure.targetAnatomicSiteCode
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/Procedure.TargetSiteCode
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:DefinedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
false
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for a procedure.
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
bilateral
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
left
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
right
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
urn:CTRv1.0:DefinedProcedure.targetAnatomicSiteLateralityCode
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:DefinedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:DefinedRepeatActivityUntilRule.cessationPauseQuantityRange
cessationPauseQuantityRange
bridg:DefinedRepeatActivityUntilRule.cessationPauseQuantityRange
false
bridg:DefinedRepeatActivityUntilRule.cessationPauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time after the observed result occurs and before the cessation of repeating the activity.
bridg:DefinedRepeatActivityUntilRule.cessationPauseQuantityRange
Stop 20 days after the observed event occurs.
bridg:DefinedRepeatActivityUntilRule.cessationPauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:DefinedRepeatActivityUntilRule.checkpointCode
checkpointCode
bridg:DefinedRepeatActivityUntilRule.checkpointCode
false
bridg:DefinedRepeatActivityUntilRule.checkpointCode
bridg:DefinedRepeatActivityUntilRule.checkpointCode
The checkpointCode specifies when the precondition is to be checked; it is analogous to the various conditional statements and loop constructs in programming languages "while-do" vs. "do-while" or "repeat-until" vs. "loop-exit."
bridg:DefinedRepeatActivityUntilRule.checkpointCode
urn:HL7SDr1:Precondition3.checkpointCode
bridg:DefinedRepeatActivityUntilRule.priorityNumber
priorityNumber
bridg:DefinedRepeatActivityUntilRule.priorityNumber
false
bridg:DefinedRepeatActivityUntilRule.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:DefinedRepeatActivityUntilRule.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:DefinedRepeatActivityUntilRule.priorityNumber
urn:HL7SDr1:Precondition3.priorityNumber
bridg:DefinedSubstanceAdministration.doseFrequencyCode
doseFrequencyCode
bridg:DefinedSubstanceAdministration.doseFrequencyCode
false
bridg:DefinedSubstanceAdministration.doseFrequencyCode
A coded value specifying how often doses are administered.
bridg:DefinedSubstanceAdministration.doseFrequencyCode
BID
bridg:DefinedSubstanceAdministration.doseFrequencyCode
TID
bridg:DefinedSubstanceAdministration.doseFrequencyCode
QID
bridg:DefinedSubstanceAdministration.doseFrequencyCode
urn:CTRPv1.0:SubstanceAdministration.doseFrequencyCode
bridg:DefinedSubstanceAdministration.doseFrequencyCode
urn:CTRPv3.8:PlannedSubstanceAdministration.doseFrequencyCode
bridg:DefinedSubstanceAdministration.doseFrequencyCode
urn:CTRv1.0:DefinedSubstanceAdministration.doseFrequencyCode
bridg:DefinedSubstanceAdministration.doseFrequencyCode
urn:HCTv1.0:CDE_2965486:Therapies.What_was_the_fractional_schedule_of_radiation_therapy?
bridg:DefinedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_DOSFRQ
bridg:DefinedSubstanceAdministration.dosePeriodCode
dosePeriodCode
bridg:DefinedSubstanceAdministration.dosePeriodCode
false
bridg:DefinedSubstanceAdministration.dosePeriodCode
A coded value specifying the period during which the dose total is administered.
bridg:DefinedSubstanceAdministration.dosePeriodCode
daily
bridg:DefinedSubstanceAdministration.dosePeriodCode
course
bridg:DefinedSubstanceAdministration.dosePeriodCode
urn:BRIDGSCC:Model_Integrity
bridg:DefinedSubstanceAdministration.dosePeriodCode
urn:CTRPv3.8:PlannedSubstanceAdministration.doseDuration
bridg:DefinedSubstanceAdministration.dosePeriodCode
urn:CTRv1.0:DefinedSubstanceAdministration.dosePeriodCode
bridg:DefinedSubstanceAdministration.doseRegimen
doseRegimen
bridg:DefinedSubstanceAdministration.doseRegimen
false
bridg:DefinedSubstanceAdministration.doseRegimen
Text description of the intended schedule for administering a substance.
bridg:DefinedSubstanceAdministration.doseRegimen
2 weeks on
bridg:DefinedSubstanceAdministration.doseRegimen
2 weeks off
bridg:DefinedSubstanceAdministration.doseRegimen
This represents the dosing calendar in a text format. This is a non-computational description that may need to be expanded as additional use cases arise.
bridg:DefinedSubstanceAdministration.doseRegimen
urn:CTRPv1.0:SubstanceAdministration.doseRegimen
bridg:DefinedSubstanceAdministration.doseRegimen
urn:CTRPv3.8:PlannedSubstanceAdministration.doseRegimen
bridg:DefinedSubstanceAdministration.doseRegimen
urn:CTRR:Comparator_Route_of_administration_-_Add_dosage/regimen_info
bridg:DefinedSubstanceAdministration.doseRegimen
urn:CTRR:Dose_regimen
bridg:DefinedSubstanceAdministration.doseRegimen
urn:CTRRr3:DefinedSubstanceAdministration.doseRegimen
bridg:DefinedSubstanceAdministration.doseRegimen
urn:CTRv1.0:DefinedSubstanceAdministration.doseRegimen
bridg:DefinedSubstanceAdministration.doseRegimen
urn:NCI_CRF_Standard:CDE_2871669v1.0:_Treatment_Regimen_Name
bridg:DefinedSubstanceAdministration.doseRegimen
urn:SDTM_IGv3.1.1:CM.CMDOSRGM
bridg:DefinedSubstanceAdministration.doseRegimen
urn:SDTM_IGv3.1.2:EX.EXDOSRGM
bridg:DefinedSubstanceAdministration.doseRegimen
urn:SDTM_IGv3.1.2:CM.CMDOSRGM
bridg:DefinedSubstanceAdministration.flowRate
flowRate
bridg:DefinedSubstanceAdministration.flowRate
false
bridg:DefinedSubstanceAdministration.flowRate
A ratio specifying the speed with which the substance is introduced into the subject.
bridg:DefinedSubstanceAdministration.flowRate
100 mL/h
bridg:DefinedSubstanceAdministration.flowRate
1 g/d
bridg:DefinedSubstanceAdministration.flowRate
40 mmol/h
bridg:DefinedSubstanceAdministration.flowRate
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.rateQuantity
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
periodProductDoseTotal
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
false
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
Total of all doses of this agent in a given period of time.
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
The given period of time is defined in dosePeriodCode.
This is needed because the dose may not always be derivable, e.g., if it is a string, and because it is often used as a cross-check on dose to ensure mistakes are not made in dosing subjects.
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTR_Rr2:Maximum_dose_per_Day_or_Total
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTR_Rr2:First_dose_in_FIH_Dose_per_Day_or_Total
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTR_Rr2:First_dose_in_FIH_Total_Dose_Unit
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTRPv1.0:SubstanceAdministration.doseTotal
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTRPv3.8:PlannedSubstanceAdministration.doseTotal
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTRRr3:DefinedSubstanceAdministration.dailyDoseTotal
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:CTRv1.0:DefinedSubstanceAdministration.periodProductDoseTotal
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.doseCheckQuantity
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_3040382:Preparative_Regimen.What_was_the_planned_total_dosage_of_the_radiolabeled_monoclonal_antibody_preparative_regimen?
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_3040323:Preparative_Regimen.What_was_the_total_dose_of_the_planned_preparative_regimen_per_the_protocol?
per the protocol?
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2685003:Preparative_Regimen.What_was_the_total_prescribed_cumulative_dose_of_total_nodal_or_total_abdominal_irradiation_for_the_preparative_regimen
per the protocol?
bridg:DefinedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2685005:Preparative_Regimen.What_was_the_unit_of_measure_for_the_total_prescribed_cumulative_dose_of_total_nodal_or_total_abdominal_irradiation_for_the_preparative_regimen
bridg:DefinedSubstanceAdministration.productDose
productDose
bridg:DefinedSubstanceAdministration.productDose
false
bridg:DefinedSubstanceAdministration.productDose
The quantity of a substance or medication to be administered.
bridg:DefinedSubstanceAdministration.productDose
5 mg
bridg:DefinedSubstanceAdministration.productDose
20 mg of drug per kg of subject weight
bridg:DefinedSubstanceAdministration.productDose
DefinedSubstanceAdministration.productDose can contain a dose expressed in absolute or relative terms (e.g., mg or mg/kg). ScheduledSubstanceAdministration.activeIngredientDose and PerformedSubstanceAdministration.productDose must contain a dose expressed in absolute terms (e.g., mg). If the DefinedSubstanceAdministration.productDose was expressed in relative terms (e.g., mg/kg), then the absolute dose must have been calculated using one or more observed factors as identified by the DefinedExpressionVariableRelationship.
First In Human dose allowed
bridg:DefinedSubstanceAdministration.productDose
urn:CTR_Rr2:First_dose_in_FIH
bridg:DefinedSubstanceAdministration.productDose
urn:CTR_Rr2:Maximum_dose_Total_Dose_Unit
bridg:DefinedSubstanceAdministration.productDose
urn:CTRPv1.0:SubstanceAdministration.dose
bridg:DefinedSubstanceAdministration.productDose
urn:CTRPv3.8:PlannedSubstanceAdministration.dose
bridg:DefinedSubstanceAdministration.productDose
urn:CTRRr3:DefinedSubstanceAdministration.dose
bridg:DefinedSubstanceAdministration.productDose
urn:CTRv1.0:DefinedSubstanceAdministration.productDose
bridg:DefinedSubstanceAdministration.productDose
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.doseQuantity
bridg:DefinedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2738649:Preparative_Regimen.What_was_the_unit_of_measure_for_the_planned_dosage_of_the_anthracycline_preparative_regimen?
per the protocol?
bridg:DefinedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2684897:Preparative_Regimen.What_was_the_total_prescribed_cumulative_dose_of_total_body_irradiation_for_the_preparative_regimen
bridg:DefinedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2740606:Preparative_Regimen.What_was_the_unit_of_measure_for_the_preparative_regimen_dose_per_the_protocol?
bridg:DefinedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2741600:Preparative_Regimen.What_was_the_unit_of_measure_for_the_planned_dosage_of_the_radiolabeled_monoclonal_antibody_preparative_regimen?
per the protocol?
bridg:DefinedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2684983:Preparative_Regimen.What_was_the_unit_of_measure_for_the_total_prescribed_cumulative_dose_of_total_body_irradiation_for_the_preparative_regimen
bridg:DefinedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2741499:Preparative_Regimen.What_was_the_unit_of_measure_for_the_planned_dosage_of_the_monoclonal_antibody_preparative_regimen?
bridg:DefinedSubstanceAdministration.productDose
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_DOSU
bridg:DefinedSubstanceAdministration.productDose
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_DOSE
bridg:DefinedSubstanceAdministration.productDose
urn:caAERSv2.2:Dose.amount
bridg:DefinedSubstanceAdministration.productDose
urn:caAERSv2.2:Dose.unit
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
routeOfAdministrationCode
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
false
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
A coded value specifying the physiological path or method of introducing the substance.
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
oral
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
intravenous
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
nasal
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
intradermal
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
intracardial
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTR_Rr2:IMP_Routes_of_Administration
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTR_Rr2:Placebo_Route_of_administration
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTR_Rr2:First_dose_in_FIH_RoA
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTR_Rr2:Maximum_dose_RoA
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTRPv1.0:SubstanceAdministration.routeOfAdministrationCode
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTRPv3.8:PlannedSubstanceAdministration.routeOfAdministrationCode
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTRR:Comparator_Route_of_administration_-_Add_dosage/regimen_info
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTRR:Route_of_administration
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTRRr3:DefinedSubstanceAdministration.routeOfAdministrationCode
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:CTRv1.0:DefinedSubstanceAdministration.routeOfAdministrationCode
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.routeCode
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:HCTv1.0:CDE_2740971:Preparative_Regimen.What_was_the_route_of_administration_for_the_planned_preparative_regimen_medication?
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_ROUTE
bridg:DefinedSubstanceAdministration.routeOfAdministrationCode
urn:caAERSv2.2:Dose.route
bridg:Device.age
age
bridg:Device.age
true
bridg:Device.age
A measure (or best estimate) of the length of time during which a device existed, measured from manufacture date (and time) to a given date (and time) of use.
bridg:Device.age
Derived from the difference between the manufacture date and the date of the activity in which it is used. This is not really a characteristic of the device since the device could be used in multiple activities.
bridg:Device.age
urn:AE:Device.deviceAge
bridg:Device.age
urn:CTRPv1.0:Device.deviceAge
bridg:Device.age
urn:CTRv1.0:Device.age
bridg:Device.availableForEvaluationIndicator
availableForEvaluationIndicator
bridg:Device.availableForEvaluationIndicator
false
bridg:Device.availableForEvaluationIndicator
Specifies whether or not the device is accessible for assessment by the manufacturer.
bridg:Device.availableForEvaluationIndicator
urn:AE:Device.availableForEvaluationIndicator
bridg:Device.availableForEvaluationIndicator
urn:CTRPv1.0:Device.availableForEvaluationIndicator
bridg:Device.availableForEvaluationIndicator
urn:CTRv1.0:Device.availableForEvaluationIndicator
bridg:Device.ceMarkIndicator
ceMarkIndicator
bridg:Device.ceMarkIndicator
false
bridg:Device.ceMarkIndicator
Specifies whether this device bears a CE (Conformite Europeenne) mark.
bridg:Device.ceMarkIndicator
CE is a mark for device products placed on the market in the European Economic Area (EEA). By placing the CE marking on a product, the manufacturer affirms that the product conforms with the requirements of the applicable European Community directives.
bridg:Device.ceMarkIndicator
urn:CTRRr3:Device.ceMarkIndicator
bridg:Device.handlingCode
handlingCode
bridg:Device.handlingCode
false
bridg:Device.handlingCode
A coded value specifying special handling requirements for the device.
bridg:Device.handlingCode
keep at room temperature
bridg:Device.handlingCode
store upright
bridg:Device.handlingCode
urn:CTRv1.0:Device.handlingCode
in R_Product
bridg:Device.handlingCode
urn:ICSRr2:Product.handlingCode
bridg:Device.manufactureDate
manufactureDate
bridg:Device.manufactureDate
false
bridg:Device.manufactureDate
The date (and time) on which the device is made.
bridg:Device.manufactureDate
urn:AE:Device.manufactureDate
bridg:Device.manufactureDate
urn:CTRPv1.0:Device.manufactureDate
bridg:Device.manufactureDate
urn:CTRv1.0:Device.manufactureDate
bridg:Device.overTheCounterProductIndicator
overTheCounterProductIndicator
bridg:Device.overTheCounterProductIndicator
false
bridg:Device.overTheCounterProductIndicator
Specifies whether a device is available over-the-counter.
bridg:Device.overTheCounterProductIndicator
urn:AE:Device.overTheCounterProductIndicator
bridg:Device.overTheCounterProductIndicator
urn:CTRPv1.0:Device.overTheCounterProductIndicator
bridg:Device.overTheCounterProductIndicator
urn:CTRv1.0:Device.overTheCounterProductIndicator
bridg:Device.reprocessedDeviceCode
reprocessedDeviceCode
bridg:Device.reprocessedDeviceCode
false
bridg:Device.reprocessedDeviceCode
A coded value specifying whether a device is reconditioned.
bridg:Device.reprocessedDeviceCode
initial use of device
bridg:Device.reprocessedDeviceCode
reuse
bridg:Device.reprocessedDeviceCode
unknown
bridg:Device.reprocessedDeviceCode
urn:AE:Device.reprocessedDeviceCode
bridg:Device.reprocessedDeviceCode
urn:CTRPv1.0:Device.reprocessedDeviceCode
bridg:Device.reprocessedDeviceCode
urn:CTRv1.0:Device.reprocessedDeviceCode
bridg:Device.returnedToReprocessorDate
returnedToReprocessorDate
bridg:Device.returnedToReprocessorDate
false
bridg:Device.returnedToReprocessorDate
The date (and time) on which the device was returned to the manufacturer or reprocessor.
bridg:Device.returnedToReprocessorDate
urn:CTRv1.0:Device.returnedToReprocessorDate
bridg:Device.returnedToReprocessorDate
urn:caAERSv2.2:MedicalDevice.returnedDate
bridg:Device.riskCode
riskCode
bridg:Device.riskCode
false
bridg:Device.riskCode
A coded value specifying the type of hazard or threat associated with the device.
bridg:Device.riskCode
flammable
bridg:Device.riskCode
explosive
bridg:Device.riskCode
urn:CTRv1.0:Device.riskCode
in R_Product
bridg:Device.riskCode
urn:ICSRr2:Product.riskCode
bridg:Device.singleUseDeviceIndicator
singleUseDeviceIndicator
bridg:Device.singleUseDeviceIndicator
false
bridg:Device.singleUseDeviceIndicator
Specifies whether a device is intended to be used only one time.
bridg:Device.singleUseDeviceIndicator
urn:AE:Device.singleUseDeviceIndicator
bridg:Device.singleUseDeviceIndicator
urn:CTRPv1.0:Device.singleUseDeviceIndicator
bridg:Device.singleUseDeviceIndicator
urn:CTRv1.0:Device.singleUseDeviceIndicator
bridg:Document.typeCode
typeCode
bridg:Document.typeCode
false
bridg:Document.typeCode
A coded value specifying the kind of document.
bridg:Document.typeCode
amendment
bridg:Document.typeCode
background material
bridg:Document.typeCode
guide
bridg:Document.typeCode
Data Clarification Form (DCF)
bridg:Document.typeCode
regulatory record
bridg:Document.typeCode
In RPS, this is the code that specifies how the file is to be used within the submission process (e.g. Protocol, Summary Introduction). Also known as context of use.
RegulatoryRecord - A document that meets a recording requirement of a regulatory authority and must be retained in accordance with that agency's records retention requirements
bridg:Document.typeCode
urn:AE:AmendmentFollowUpReport
bridg:Document.typeCode
urn:C3PRv2.9:StudyVersion.amendmentType
bridg:Document.typeCode
urn:CTRPv1.0:Document.typeCode
bridg:Document.typeCode
urn:CTRPv3.8:Document.typeCode
bridg:Document.typeCode
urn:CTRRr3:Document.typeCode
bridg:Document.typeCode
urn:CTRv1.0:Document.typeCode
bridg:Document.typeCode
urn:HL7SD:ReplacementOf1.typeCode
in IndividualCaseSafetyReport
bridg:Document.typeCode
urn:ICSRr2:ControlActEvent.code
in IndividualCaseSafetyReport
bridg:Document.typeCode
urn:ICSRr2:document.code
bridg:Document.typeCode
urn:RPS1:Documentation.context
bridg:Document.typeCode
urn:Statistics_v1.0:Document.typeCode
bridg:DocumentIdentifier.identifier
identifier
bridg:DocumentIdentifier.identifier
false
bridg:DocumentIdentifier.identifier
A unique symbol that establishes identity of the document.
bridg:DocumentIdentifier.identifier
A study protocol identifier is assigned by the National Cancer Institute (NCI).
bridg:DocumentIdentifier.identifier
A particular document can have one or more ID.
bridg:DocumentIdentifier.identifier
urn:AE:Study.additionalIdentifier
bridg:DocumentIdentifier.identifier
urn:AE:SafetyReport.identifier
bridg:DocumentIdentifier.identifier
urn:AE:Study.primaryIdentifier
bridg:DocumentIdentifier.identifier
urn:AE:SafetyReport.alternateIdentifier
bridg:DocumentIdentifier.identifier
urn:AE:AmendmentFollowUpReport.reportAmendedIdentifier
bridg:DocumentIdentifier.identifier
urn:C3PR:Identifier.value
bridg:DocumentIdentifier.identifier
urn:C3PRv2.9:Identifier.value
bridg:DocumentIdentifier.identifier
urn:C3PRv2.9:RemoteStudy.externalId
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:MB.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:SU.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:CM.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:EX.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:IE.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:DS.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:LB.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:DA.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:DV.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:VS.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:PE.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:SC.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:QS.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:MH.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:DM.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:AE.STUDYID
bridg:DocumentIdentifier.identifier
urn:CDASHv1.1:EG.STUDYID
bridg:DocumentIdentifier.identifier
urn:CTGOV:Organization's_Unique_Protocol_ID
bridg:DocumentIdentifier.identifier
urn:CTGOV:Secondary_IDs
bridg:DocumentIdentifier.identifier
urn:CTGOV:IND/IDE_Serial_Number
bridg:DocumentIdentifier.identifier
urn:CTOM:Protocol.nciIdentifier
bridg:DocumentIdentifier.identifier
urn:CTOM:Protocol.navyNCIIdentifier
bridg:DocumentIdentifier.identifier
urn:CTOM:PartcipantEligibilityAnswer.checklistNumber
bridg:DocumentIdentifier.identifier
urn:CTOM:StudySite.localProtocolIdentifier
bridg:DocumentIdentifier.identifier
urn:CTR_Rr2:EudraCT_number
bridg:DocumentIdentifier.identifier
urn:CTR_Rr2:WHO_UTRN
bridg:DocumentIdentifier.identifier
urn:CTR_Rr2:Other_Identifier
bridg:DocumentIdentifier.identifier
urn:CTR_Rr2:US_NCT_number
bridg:DocumentIdentifier.identifier
urn:CTR_Rr2:Sponsor_protocol_number
bridg:DocumentIdentifier.identifier
urn:CTR_Rr2:ISRCTN_number
bridg:DocumentIdentifier.identifier
urn:CTRPv1.0:Document.identifier
bridg:DocumentIdentifier.identifier
urn:CTRPv1.0:InterventionalStudyProtocol.identifier
bridg:DocumentIdentifier.identifier
urn:CTRPv1.0:ObservationalStudyProtocol.identifier
bridg:DocumentIdentifier.identifier
urn:CTRPv1.0:StudyParticipation.localStudyProtocolIdentifier
bridg:DocumentIdentifier.identifier
urn:CTRPv1.0:StudyProtocol.identifier
bridg:DocumentIdentifier.identifier
urn:CTRPv3.8:Document.identifier
bridg:DocumentIdentifier.identifier
urn:CTRPv3.8:StudyProtocol.otherIdentifiers
bridg:DocumentIdentifier.identifier
urn:CTRPv3.8:StudyProtocol.assignedIdentifier
bridg:DocumentIdentifier.identifier
urn:CTRR:Registry_Protocol_Identifier
bridg:DocumentIdentifier.identifier
urn:CTRR:Protocol_Identifier
bridg:DocumentIdentifier.identifier
urn:CTRRr3:DocumentIdentifier.identifier
bridg:DocumentIdentifier.identifier
urn:CTRRr3:StudyAgent.expandedAccessRecordIdentifier
bridg:DocumentIdentifier.identifier
urn:CTRv1.0:DocumentIdentifier.identifier
bridg:DocumentIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.setID
bridg:DocumentIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.id
bridg:DocumentIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:relatedDocument.id
bridg:DocumentIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:relatedDocument.setId
bridg:DocumentIdentifier.identifier
urn:HCTv1.0:CDE_2692926:Recipient_Identification.Study_ID__What_is_the_study_ID_number?
bridg:DocumentIdentifier.identifier
urn:HL7SD:PlannedStudy.setID
bridg:DocumentIdentifier.identifier
urn:HL7SP:PlannedStudy.id
bridg:DocumentIdentifier.identifier
urn:HL7SP:Study.id
bridg:DocumentIdentifier.identifier
urn:HSDBv1.0:[Study].Lead_Organization_Trial_Identifier
bridg:DocumentIdentifier.identifier
urn:HSDBv1.0:[Sponsor].Sponsor_protocol_no
bridg:DocumentIdentifier.identifier
urn:HSDBv1.0:[Study].Unique_Trial_Identifier
in IndividualCaseSafetyReport
bridg:DocumentIdentifier.identifier
urn:ICSRr2:ResearchStudy.id
in IndividualCaseSafetyReport
bridg:DocumentIdentifier.identifier
urn:ICSRr2:InvestigativeEvent.id
in IndividualCaseSafetyReport
bridg:DocumentIdentifier.identifier
urn:ICSRr2:ControlActEvent.id
in IndividualCaseSafetyReport
bridg:DocumentIdentifier.identifier
urn:ICSRr2:StudyRegistration.id
bridg:DocumentIdentifier.identifier
urn:ICSRr2:StudyRegistration.id
in IndividualCaseSafetyReport
bridg:DocumentIdentifier.identifier
urn:ICSRr2:document.id
in IndividualCaseSafetyReport
bridg:DocumentIdentifier.identifier
urn:ICSRr2:RelatedInvestigation.id
bridg:DocumentIdentifier.identifier
urn:Lab:Study.identifier
bridg:DocumentIdentifier.identifier
urn:LabViewer2.2:Identifier.displayable
bridg:DocumentIdentifier.identifier
urn:LabViewer2.2:Identifier.root
bridg:DocumentIdentifier.identifier
urn:LabViewer2.2:Identifier.extension
bridg:DocumentIdentifier.identifier
urn:NCI_CRF_Standard:CDE_3008882v1.0:_Case_Report_Form_Identifier
bridg:DocumentIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2746459v1.0:_Protocol_Clinical_Study_Identifier_Number
bridg:DocumentIdentifier.identifier
urn:PSCv2.6:Study.assignedIdentifier
bridg:DocumentIdentifier.identifier
urn:PSCv2.6:StudySecondaryIdentifier.value
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:LB.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:TI.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:EG.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:TA.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:MH.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:DS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:DV.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:DM.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:EX.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:QS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:TE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:PE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:SV.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:SE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:IE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:AE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:CM.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:CO.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:TV.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:SU.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:SC.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:DA.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:VS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.1:TS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:PE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:CE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:PC.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:TS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:IE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:SV.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:FA.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:MS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:QS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:VS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:CM.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:TI.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:DS.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:AE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:LB.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:CO.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:DA.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:EX.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:DM.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:SU.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:SC.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:DV.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:SE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:MB.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:PP.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:TV.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:TA.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:TE.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:MH.STUDYID
bridg:DocumentIdentifier.identifier
urn:SDTM_IGv3.1.2:EG.STUDYID
bridg:DocumentIdentifier.identifier
urn:Statistics_v1.0:DocumentIdentifier.identifier
bridg:DocumentIdentifier.identifier
urn:WHO:Primary_Registry_and_Trial_Identifying_Number
bridg:DocumentIdentifier.identifier
urn:WHO:Secondary_Identifying_Numbers
bridg:DocumentIdentifier.identifier
urn:caAERSv2.2:Identifier.value___Study
bridg:DocumentIdentifier.primaryIndicator
primaryIndicator
bridg:DocumentIdentifier.primaryIndicator
false
bridg:DocumentIdentifier.primaryIndicator
Specifies whether this is the main or principal document identifier.
bridg:DocumentIdentifier.primaryIndicator
primaryIndicator may only apply for a given typeCode.
bridg:DocumentIdentifier.primaryIndicator
urn:C3PR:Identifier.isPrimary
bridg:DocumentIdentifier.primaryIndicator
urn:C3PRv2.9:Identifier.primaryIndicator
bridg:DocumentIdentifier.primaryIndicator
urn:CTRR:Registry_Type_Code
bridg:DocumentIdentifier.primaryIndicator
urn:CTRv1.0:DocumentIdentifier.primaryIndicator
bridg:DocumentIdentifier.primaryIndicator
urn:Statistics_v1.0:DocumentIdentifier.primaryIndicator
bridg:DocumentIdentifier.primaryIndicator
urn:caAERSv2.2:Identifier.isPrimary___Study
bridg:DocumentIdentifier.typeCode
typeCode
bridg:DocumentIdentifier.typeCode
false
bridg:DocumentIdentifier.typeCode
A coded value specifying the kind of document identifier.
bridg:DocumentIdentifier.typeCode
sponsor protocol number
bridg:DocumentIdentifier.typeCode
national number
bridg:DocumentIdentifier.typeCode
cooperative group protocol number
bridg:DocumentIdentifier.typeCode
CDISC protocol identifying number
bridg:DocumentIdentifier.typeCode
registry identifier
bridg:DocumentIdentifier.typeCode
urn:C3PR:Identifier.type
bridg:DocumentIdentifier.typeCode
urn:C3PRv2.9:Identifier.typeInternal
bridg:DocumentIdentifier.typeCode
urn:C3PRv2.9:OrganizationAssignedIdentifier
bridg:DocumentIdentifier.typeCode
urn:CTR_Rr2:Other_Identifier_Name
bridg:DocumentIdentifier.typeCode
urn:CTRRr3:DocumentIdentifier.typeCode
bridg:DocumentIdentifier.typeCode
urn:CTRv1.0:DocumentIdentifier.typeCode
bridg:DocumentIdentifier.typeCode
urn:PSCv2.6:StudySecondaryIdentifier.name
bridg:DocumentIdentifier.typeCode
urn:PSCv2.6:Study.provider
bridg:DocumentIdentifier.typeCode
urn:Statistics_v1.0:DocumentIdentifier.typeCode
bridg:DocumentIdentifier.typeCode
urn:caAERSv2.2:Identifier.type___Study
bridg:DocumentVersion.bibliographicDesignation
bibliographicDesignation
bridg:DocumentVersion.bibliographicDesignation
false
bridg:DocumentVersion.bibliographicDesignation
A text block containing publishing and authoring information that allows receivers of this document version to refer appropriately to this document version.
bridg:DocumentVersion.bibliographicDesignation
Good Health Hospital IRB Minutes
bridg:DocumentVersion.bibliographicDesignation
18-Jan-2008
bridg:DocumentVersion.bibliographicDesignation
urn:CTRPv1.0:ObservationalStudyProtocol.bibliographicDesignation
bridg:DocumentVersion.bibliographicDesignation
urn:CTRPv1.0:InterventionalStudyProtocol.bibliographicDesignation
bridg:DocumentVersion.bibliographicDesignation
urn:CTRPv1.0:StudyProtocol.bibliographicDesignation
bridg:DocumentVersion.bibliographicDesignation
urn:CTRPv3.8:StudyProtocol.bibliographicDesignation
bridg:DocumentVersion.bibliographicDesignation
urn:CTRv1.0:DocumentVersion.bibliographicDesignation
in IndividualCaseSafetyReport
bridg:DocumentVersion.bibliographicDesignation
urn:ICSRr2:document.bibliographicDesignationText
bridg:DocumentVersion.bibliographicDesignation
urn:Statistics_v1.0:DocumentVersion.bibliographicDesignation
bridg:DocumentVersion.confidentialityCode
confidentialityCode
bridg:DocumentVersion.confidentialityCode
false
bridg:DocumentVersion.confidentialityCode
A coded value specifying the degree of sensitivity associated with the document.
bridg:DocumentVersion.confidentialityCode
Normal
bridg:DocumentVersion.confidentialityCode
Restricted
bridg:DocumentVersion.confidentialityCode
Very Restricted
bridg:DocumentVersion.confidentialityCode
urn:CTRv1.0:DocumentVersion.confidentialityCode
bridg:DocumentVersion.confidentialityCode
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.confidentialityCode
in IndividualCaseSafetyReport
bridg:DocumentVersion.confidentialityCode
urn:ICSRr2:ControlActEvent.confidentialityCode
bridg:DocumentVersion.date
date
bridg:DocumentVersion.date
false
bridg:DocumentVersion.date
The date (and time) on which the document is versioned.
bridg:DocumentVersion.date
urn:CTR_Rr2:Sponsor_protocol_version_date
bridg:DocumentVersion.date
urn:CTRPv3.8:StudyProtocol.amendmentDate
bridg:DocumentVersion.date
urn:CTRR:Sponsor_Protocol_Version_Date
bridg:DocumentVersion.date
urn:CTRRr3:Document.versionDate
bridg:DocumentVersion.date
urn:CTRv1.0:DocumentVersion.date
bridg:DocumentVersion.date
urn:HCTv1.0:CDE_2768219:Medical_Records_and_Forms.What_is_the_post_transplantation_time_period_for_this_follow_up_report?
in IndividualCaseSafetyReport
bridg:DocumentVersion.date
urn:ICSRr2:RelatedInvestigation.availabilityTime
in IndividualCaseSafetyReport
bridg:DocumentVersion.date
urn:ICSRr2:InvestigativeEvent.availabilityTime
bridg:DocumentVersion.date
urn:LabViewer2.2:Study.amendmentDate
bridg:DocumentVersion.date
urn:NCI_CRF_Standard:CDE_3008890v1.0:_Case_Report_Form_Version_Date
bridg:DocumentVersion.date
urn:PSCv2.6:Amendment.date
bridg:DocumentVersion.date
urn:Statistics_v1.0:DocumentVersion.date
bridg:DocumentVersion.date
urn:caAERSv2.2:ReportVersion.createdOn
bridg:DocumentVersion.date
urn:caAERSv2.2:Report.createdOn
bridg:DocumentVersion.keywordCode
keywordCode
bridg:DocumentVersion.keywordCode
false
bridg:DocumentVersion.keywordCode
A coded value specifying the words or phrases that best describe the document and/or its context. Keywords help users find documents of interest.
bridg:DocumentVersion.keywordCode
species
bridg:DocumentVersion.keywordCode
indication
bridg:DocumentVersion.keywordCode
biocompatibility
bridg:DocumentVersion.keywordCode
drug substance
bridg:DocumentVersion.keywordCode
drug product
bridg:DocumentVersion.keywordCode
urn:CTGOV:Keywords
bridg:DocumentVersion.keywordCode
urn:CTRPv1.0:InterventionalStudyProtocol.keywordCode
bridg:DocumentVersion.keywordCode
urn:CTRPv1.0:StudyProtocol.keywordCode
bridg:DocumentVersion.keywordCode
urn:CTRPv1.0:ObservationalStudyProtocol.keywordCode
bridg:DocumentVersion.keywordCode
urn:CTRR:Keywords
bridg:DocumentVersion.keywordCode
urn:CTRv1.0:DocumentVersion.keywordCode
bridg:DocumentVersion.keywordCode
urn:RPS1:Keyword.code
bridg:DocumentVersion.keywordCode
urn:Statistics_v1.0:DocumentVersion.keywordCode
bridg:DocumentVersion.keywordCode
urn:WHO:Keyword
bridg:DocumentVersion.keywordText
keywordText
bridg:DocumentVersion.keywordText
false
bridg:DocumentVersion.keywordText
A character string of a word or phrase that describes the document and/or its context. Keywords help users find documents of interest.
bridg:DocumentVersion.keywordText
species
bridg:DocumentVersion.keywordText
indication
bridg:DocumentVersion.keywordText
biocompatibility
bridg:DocumentVersion.keywordText
drug substance
bridg:DocumentVersion.keywordText
drug product
bridg:DocumentVersion.keywordText
urn:CTGOV:Keywords
bridg:DocumentVersion.keywordText
urn:CTRPv1.0:StudyProtocol.keywordText
bridg:DocumentVersion.keywordText
urn:CTRPv1.0:ObservationalStudyProtocol.keywordText
bridg:DocumentVersion.keywordText
urn:CTRPv1.0:InterventionalStudyProtocol.keywordText
bridg:DocumentVersion.keywordText
urn:CTRPv3.8:StudyProtocol.keywordText
bridg:DocumentVersion.keywordText
urn:CTRR:Keywords
bridg:DocumentVersion.keywordText
urn:CTRRr3:Document.keywordText
bridg:DocumentVersion.keywordText
urn:CTRv1.0:DocumentVersion.keywordText
bridg:DocumentVersion.keywordText
urn:RPS1:Keyword.textValue
bridg:DocumentVersion.keywordText
urn:Statistics_v1.0:DocumentVersion.keywordText
bridg:DocumentVersion.languageCode
languageCode
bridg:DocumentVersion.languageCode
false
bridg:DocumentVersion.languageCode
A coded value specifying the language that the document is written in.
bridg:DocumentVersion.languageCode
English
bridg:DocumentVersion.languageCode
German
bridg:DocumentVersion.languageCode
This attribute is used to indicate the language in which all (or most) of the discrete data elements that make up the document are expressed. This is distinct from the DocumentVersion.text(ED).languageCode property which expresses the language in which the document is rendered. This attribute is most important in circumstances where the document is not rendered.
bridg:DocumentVersion.languageCode
urn:CTRv1.0:DocumentVersion.languageCode
bridg:DocumentVersion.languageCode
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.languageCode
bridg:DocumentVersion.languageCode
urn:Statistics_v1.0:DocumentVersion.language
bridg:DocumentVersion.numberText
numberText
bridg:DocumentVersion.numberText
false
bridg:DocumentVersion.numberText
A character string that identifies a given collection of content of a document at a point in time.
bridg:DocumentVersion.numberText
In RPS this could be implemented as follows: The version number would be an integer starting at '1' and incrementing by 1. The first instance or original report should always be valued as '1'. The version number value must be incremented by one when a report is replaced
bridg:DocumentVersion.numberText
but can also be incremented more often to meet local requirements.
bridg:DocumentVersion.numberText
Different versions of the same document belong to the same document group.
Over time, there may be multiple changes to a document, and the version allows an individual to capture relationships between changes in the instances of a document over time. There can be a new version every time the content changes.
bridg:DocumentVersion.numberText
urn:AE:SafetyReport.initialReportIndicator
bridg:DocumentVersion.numberText
urn:C3PR:StudySubject.informedConsentVersion
bridg:DocumentVersion.numberText
urn:C3PR:Study.consentVersion
bridg:DocumentVersion.numberText
urn:C3PRv2.9:StudyVersion.name
bridg:DocumentVersion.numberText
urn:CTOM:Protocol.amendmentIdentifier
bridg:DocumentVersion.numberText
urn:CTR_Rr2:Sponsor_protocol_version
bridg:DocumentVersion.numberText
urn:CTRPv1.0:InterventionalStudyProtocol.revision
bridg:DocumentVersion.numberText
urn:CTRPv1.0:ObservationalStudyProtocol.revision
bridg:DocumentVersion.numberText
urn:CTRPv1.0:StudyProtocol.revision
bridg:DocumentVersion.numberText
urn:CTRPv1.0:Document.revision
bridg:DocumentVersion.numberText
urn:CTRPv3.8:StudyProtocol.amendmentNumberText
bridg:DocumentVersion.numberText
urn:CTRRr3:Document.revisionNumberText
bridg:DocumentVersion.numberText
urn:CTRv1.0:DocumentVersion.numberText
bridg:DocumentVersion.numberText
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.versionNumber
bridg:DocumentVersion.numberText
urn:FDA_HL7_SD_SD_DSTU2012:relatedDocument.versionNumber
bridg:DocumentVersion.numberText
urn:HL7SD:PlannedStudy.versionNumber
bridg:DocumentVersion.numberText
urn:NCI_CRF_Standard:CDE_3008888v1.0:_Case_Report_Form_Version_Number
bridg:DocumentVersion.numberText
urn:PSCv2.6:Amendment.name
bridg:DocumentVersion.numberText
urn:RPS1:Documentation.version
bridg:DocumentVersion.numberText
urn:Statistics_v1.0:DocumentVersion.numberText
bridg:DocumentVersion.numberText
urn:caAERSv2.2:ReportVersion.reportVersionId
bridg:DocumentVersion.officialTitle
officialTitle
bridg:DocumentVersion.officialTitle
false
bridg:DocumentVersion.officialTitle
The formal title of the document.
bridg:DocumentVersion.officialTitle
If there is only one title, use this attribute.
bridg:DocumentVersion.officialTitle
urn:C3PR:Study.longTitleText
bridg:DocumentVersion.officialTitle
urn:C3PRv2.9:Consent.name
bridg:DocumentVersion.officialTitle
urn:C3PRv2.9:StudyVersion.longTitleText
bridg:DocumentVersion.officialTitle
urn:CTGOV:Official_Title
bridg:DocumentVersion.officialTitle
urn:CTOM:Protocol.longTitleText
bridg:DocumentVersion.officialTitle
urn:CTR_Rr2:Full_title_of_the_trial
bridg:DocumentVersion.officialTitle
urn:CTRPv1.0:InterventionalStudyProtocol.officialTitle
bridg:DocumentVersion.officialTitle
urn:CTRPv1.0:ObservationalStudyProtocol.officialTitle
bridg:DocumentVersion.officialTitle
urn:CTRPv3.8:StudyProtocol.officialTitle
bridg:DocumentVersion.officialTitle
urn:CTRRr3:Document.officialTitle
bridg:DocumentVersion.officialTitle
urn:CTRv1.0:DocumentVersion.officialTitle
bridg:DocumentVersion.officialTitle
urn:HCTv1.0:CDE_2978255:Research_Protocols.Specify_the_research_activity_the_recipient_participates_in:
bridg:DocumentVersion.officialTitle
urn:HL7SD:PlannedStudy.title
bridg:DocumentVersion.officialTitle
urn:HSDBv1.0:[Study].Study_Title
in IndividualCaseSafetyReport
bridg:DocumentVersion.officialTitle
urn:ICSRr2:document.title
in IndividualCaseSafetyReport
bridg:DocumentVersion.officialTitle
urn:ICSRr2:ResearchStudy.title
in IndividualCaseSafetyReport
bridg:DocumentVersion.officialTitle
urn:ICSRr2:RelatedInvestigation.title
bridg:DocumentVersion.officialTitle
urn:Lab:Study.name
bridg:DocumentVersion.officialTitle
urn:LabViewer2.2:Study.name
bridg:DocumentVersion.officialTitle
urn:NCI_CRF_Standard:CDE_3009034v1.0:_Case_Report_Form_Name
bridg:DocumentVersion.officialTitle
urn:PSC:Study.name
bridg:DocumentVersion.officialTitle
urn:RPS1:Documentation.title
bridg:DocumentVersion.officialTitle
urn:Statistics_v1.0:DocumentVersion.officialTitle
bridg:DocumentVersion.officialTitle
urn:WHO:Scientific_Title
bridg:DocumentVersion.officialTitle
urn:caAERSv2.2:Study.longTitleText
bridg:DocumentVersion.revisionReasonCode
revisionReasonCode
bridg:DocumentVersion.revisionReasonCode
false
bridg:DocumentVersion.revisionReasonCode
A coded value specifying why the document is revised.
bridg:DocumentVersion.revisionReasonCode
urn:C3PRv2.9:StudyVersion.AmendmentReason
bridg:DocumentVersion.revisionReasonCode
urn:CTRPv3.8:StudyProtocol.amendmentReasonCode
bridg:DocumentVersion.revisionReasonCode
urn:CTRPv3.8:Document.inactiveCommentText
bridg:DocumentVersion.revisionReasonCode
urn:CTRv1.0:DocumentVersion.revisionReason
bridg:DocumentVersion.revisionReasonCode
urn:HL7SD:PlannedStudy.reasonCode
bridg:DocumentVersion.revisionReasonCode
urn:HL7SDr1:ControlActEvent.reasonCode
in IndividualCaseSafetyReport
bridg:DocumentVersion.revisionReasonCode
urn:ICSRr2:ControlActEvent.reasonCode
bridg:DocumentVersion.revisionReasonCode
urn:Statistics_v1.0:DocumentVersion.revisionReasonCode
bridg:DocumentVersion.text
text
bridg:DocumentVersion.text
false
bridg:DocumentVersion.text
A textual or media-based representation that is the full or comprehensive narrative or content of the document.
bridg:DocumentVersion.text
urn:AE:Document.text
bridg:DocumentVersion.text
urn:AE:SafetyReport.narrativeText
bridg:DocumentVersion.text
urn:CTR_Rr2:IMP_modified_specification
bridg:DocumentVersion.text
urn:CTRPv1.0:InterventionalStudyProtocol.text
bridg:DocumentVersion.text
urn:CTRPv1.0:ObservationalStudyProtocol.text
bridg:DocumentVersion.text
urn:CTRPv1.0:StudyProtocol.text
bridg:DocumentVersion.text
urn:CTRPv3.8:Document.text
bridg:DocumentVersion.text
urn:CTRRr3:Document.text
bridg:DocumentVersion.text
urn:CTRv1.0:DocumentVersion.text
bridg:DocumentVersion.text
urn:HL7SD:PlannedStudy.text
in IndividualCaseSafetyReport
bridg:DocumentVersion.text
urn:ICSRr2:document.text
in IndividualCaseSafetyReport
bridg:DocumentVersion.text
urn:ICSRr2:RelatedInvestigation.text
in IndividualCaseSafetyReport
bridg:DocumentVersion.text
urn:ICSRr2:InvestigativeEvent.text
bridg:DocumentVersion.text
urn:Statistics_v1.0:DocumentVersion.text
bridg:DocumentVersion.text
urn:caAERSv2.2:NotificationAttachment.content
bridg:DocumentVersion.uniformResourceLocator
uniformResourceLocator
bridg:DocumentVersion.uniformResourceLocator
true
bridg:DocumentVersion.uniformResourceLocator
A complete or local reference to a website, ftp, file path or other location from which the document contents can be retrieved.
bridg:DocumentVersion.uniformResourceLocator
Derived from DocumentVersion.text.ED.reference.
Local references should only be used when communicating between systems capable of resolving the local reference.
In a Regulatory Product Submission (RPS) message, this identifies the file (with a Uniform Resource Identifier (URI)), which is part of the documentation. A URI is a compact string of characters used to identify or name a resource. The main purpose of this identification is to enable interaction with representations of the resource over a network, typically the World Wide Web, using specific protocols. URIs are defined in schemes defining a specific syntax and associated protocols.
bridg:DocumentVersion.uniformResourceLocator
urn:AE:Document.universalResourceLocator
bridg:DocumentVersion.uniformResourceLocator
urn:CTOM:Protocol.documentUri
bridg:DocumentVersion.uniformResourceLocator
urn:CTRPv1.0:Document.universalResourceLocator
bridg:DocumentVersion.uniformResourceLocator
urn:CTRPv3.8:Document.universalResourceLocator
bridg:DocumentVersion.uniformResourceLocator
urn:CTRPv3.8:Document.fileName
bridg:DocumentVersion.uniformResourceLocator
urn:CTRv1.0:DocumentVersion.uniformResourceLocator
bridg:DocumentVersion.uniformResourceLocator
urn:RPS1:Documentation.fileID
bridg:DocumentVersion.uniformResourceLocator
urn:Statistics_v1.0:DocumentVersion.uniformResourceLocator
bridg:DocumentVersionRelationship.priorityNumber
priorityNumber
bridg:DocumentVersionRelationship.priorityNumber
false
bridg:DocumentVersionRelationship.priorityNumber
A number specifying the relative rank for one document before other similar documents having the same type of association to the same source document.
bridg:DocumentVersionRelationship.priorityNumber
A report initiated by the primary physician may be ranked higher than reports initiated by specialty consultants or support staff.
bridg:DocumentVersionRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
There may be multiple investigations (and therefore reports) into the same event, each initiated by a different party. The priorityNumber may be used to rank these investigations.
The ordering may be a total ordering, in which all priority numbers are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
bridg:DocumentVersionRelationship.priorityNumber
urn:CTRPv3.8:StudyRelationship.sequenceNumber
bridg:DocumentVersionRelationship.priorityNumber
urn:CTRv1.0:DocumentVersionRelationship.priorityNumber
in IndividualCaseSafetyReport
bridg:DocumentVersionRelationship.priorityNumber
urn:ICSRr2:SourceOf1.priorityNumber
bridg:DocumentVersionRelationship.typeCode
typeCode
bridg:DocumentVersionRelationship.typeCode
false
bridg:DocumentVersionRelationship.typeCode
A coded value specifying the kind of document relationship. Each value implies specific constraints to what kinds of objects can be related and in which way.
bridg:DocumentVersionRelationship.typeCode
decomposition (component)
bridg:DocumentVersionRelationship.typeCode
pre-condition
bridg:DocumentVersionRelationship.typeCode
post-condition
bridg:DocumentVersionRelationship.typeCode
sequel (replaces
bridg:DocumentVersionRelationship.typeCode
modifies)
bridg:DocumentVersionRelationship.typeCode
attribution (cause and effect)
bridg:DocumentVersionRelationship.typeCode
This is HL7 structured vocabulary and is part of a controlled vocabulary set.
bridg:DocumentVersionRelationship.typeCode
urn:AE:SafetyReport.amendmentReportInd
bridg:DocumentVersionRelationship.typeCode
urn:CTRPv3.8:StudyRelationship.typeCode
bridg:DocumentVersionRelationship.typeCode
urn:CTRv1.0:DocumentVersionRelationship.typeCode
bridg:DocumentVersionRelationship.typeCode
urn:FDA_HL7_SD_SD_DSTU2012:outboundRelationship.typeCode
in IndividualCaseSafetyReport
bridg:DocumentVersionRelationship.typeCode
urn:ICSRr2:SourceOf2.typeCode
in IndividualCaseSafetyReport
bridg:DocumentVersionRelationship.typeCode
urn:ICSRr2:SourceOf1.typeCode
bridg:DocumentVersionRelationship.typeCode
urn:RPS1:RelatedDocumentation.relationship
bridg:DocumentVersionWorkflowStatus.code
code
bridg:DocumentVersionWorkflowStatus.code
false
bridg:DocumentVersionWorkflowStatus.code
A coded value specifying the phase in the lifecycle of the document version workflow.
bridg:DocumentVersionWorkflowStatus.code
On-hold
bridg:DocumentVersionWorkflowStatus.code
Accepted
bridg:DocumentVersionWorkflowStatus.code
Rejected
bridg:DocumentVersionWorkflowStatus.code
Abstracted
bridg:DocumentVersionWorkflowStatus.code
Abstraction Verified
bridg:DocumentVersionWorkflowStatus.code
Abstraction not verified
bridg:DocumentVersionWorkflowStatus.code
Created
bridg:DocumentVersionWorkflowStatus.code
available [examples for HL7 StudyDesign Structured Document]
bridg:DocumentVersionWorkflowStatus.code
Please refer to the Processing Status state transition diagram for further details.
A state transition diagram needs to be developed for the HL7 StudyDesign Structured Document examples.
bridg:DocumentVersionWorkflowStatus.code
urn:AE:SafetyReport.statusCode
bridg:DocumentVersionWorkflowStatus.code
urn:C3PRv2.9:StudyVersion.versionStatus
bridg:DocumentVersionWorkflowStatus.code
urn:CTOM:ProtocolStatus.statusCode
bridg:DocumentVersionWorkflowStatus.code
urn:CTRPv1.0:DocumentWorkflowStatus.statusCode
bridg:DocumentVersionWorkflowStatus.code
urn:CTRPv3.8:DocumentWorkflowStatus.statusCode
bridg:DocumentVersionWorkflowStatus.code
urn:CTRv1.0:DocumentVersionWorkflowStatus.code
bridg:DocumentVersionWorkflowStatus.code
urn:LabViewer2.2:Study.status
bridg:DocumentVersionWorkflowStatus.code
urn:caAERSv2.2:ReportVersion.status
bridg:DocumentVersionWorkflowStatus.comment
comment
bridg:DocumentVersionWorkflowStatus.comment
false
bridg:DocumentVersionWorkflowStatus.comment
Additional description of the workflow status.
bridg:DocumentVersionWorkflowStatus.comment
to capture the reasons of statuses or other notes
bridg:DocumentVersionWorkflowStatus.comment
urn:CTRPv1.0:DocumentWorkflowStatus.commentText
bridg:DocumentVersionWorkflowStatus.comment
urn:CTRPv3.8:DocumentWorkflowStatus.commentText
bridg:DocumentVersionWorkflowStatus.comment
urn:CTRv1.0:DocumentVersionWorkflowStatus.comment
bridg:DocumentVersionWorkflowStatus.date
date
bridg:DocumentVersionWorkflowStatus.date
false
bridg:DocumentVersionWorkflowStatus.date
The date (and time) on which the status is assigned to the document version workflow.
bridg:DocumentVersionWorkflowStatus.date
urn:AE:SafetyReport.mostRecentInformationDate
bridg:DocumentVersionWorkflowStatus.date
urn:AE:SafetyReport.timeReportCompleted
bridg:DocumentVersionWorkflowStatus.date
urn:C3PRv2.9:StudyVersion.versionDate
bridg:DocumentVersionWorkflowStatus.date
urn:CTOM:Protocol.amendmentDate
bridg:DocumentVersionWorkflowStatus.date
urn:CTOM:ProtocolStatus.statusDate
bridg:DocumentVersionWorkflowStatus.date
urn:CTRPv1.0:DocumentWorkflowStatus.statusDate
bridg:DocumentVersionWorkflowStatus.date
urn:CTRPv3.8:DocumentWorkflowStatus.statusDateRange
bridg:DocumentVersionWorkflowStatus.date
urn:CTRv1.0:DocumentVersionWorkflowStatus.date
bridg:DocumentVersionWorkflowStatus.date
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.availibilityTime
bridg:DocumentVersionWorkflowStatus.date
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.effectiveTime
in IndividualCaseSafetyReport
bridg:DocumentVersionWorkflowStatus.date
urn:ICSRr2:ControlActEvent.effectiveTime
bridg:DocumentVersionWorkflowStatus.date
urn:LabViewer2.2:Study.statusDate
bridg:DocumentVersionWorkflowStatus.date
urn:caAERSv2.2:ReportVersion.submittedOn
bridg:DocumentVersionWorkflowStatus.date
urn:caAERSv2.2:Report.submittedDate
bridg:DocumentVersionWorkflowStatus.date
urn:caAERSv2.2:ReportVersion.withdrawOn
bridg:Drug.actionModeCode
actionModeCode
bridg:Drug.actionModeCode
false
bridg:Drug.actionModeCode
A coded value specifying the mode of action through which this substance produces a pharmacological effect.
bridg:Drug.actionModeCode
stimulating action
bridg:Drug.actionModeCode
depressing action
bridg:Drug.actionModeCode
blocking/antagonizing action
bridg:Drug.actionModeCode
stabilizing action
bridg:Drug.actionModeCode
exchanging/replacing substances
bridg:Drug.actionModeCode
direct beneficial chemical reaction
bridg:Drug.actionModeCode
direct harmful chemical reaction.
bridg:Drug.actionModeCode
urn:CTRRr3:ProductPart.actionModeCode
bridg:Drug.handlingCode
handlingCode
bridg:Drug.handlingCode
false
bridg:Drug.handlingCode
A coded value specifying special handling requirements for the drug.
bridg:Drug.handlingCode
keep at room temperature
bridg:Drug.handlingCode
store upright
bridg:Drug.handlingCode
urn:CTRv1.0:Drug.handlingCode
in R_Product
bridg:Drug.handlingCode
urn:ICSRr2:Product.handlingCode
bridg:Drug.riskCode
riskCode
bridg:Drug.riskCode
false
bridg:Drug.riskCode
A coded value specifying the type of hazard or threat associated with the drug.
bridg:Drug.riskCode
flammable
bridg:Drug.riskCode
explosive
bridg:Drug.riskCode
urn:CTRv1.0:Drug.riskCode
in R_Product
bridg:Drug.riskCode
urn:ICSRr2:Product.riskCode
bridg:Drug.stabilityDuration
stabilityDuration
bridg:Drug.stabilityDuration
false
bridg:Drug.stabilityDuration
The period of time during which the drug is considered usable after it is activated (opened).
bridg:Drug.stabilityDuration
urn:CTRv1.0:Drug.stabilityDuration
in R_Product
bridg:Drug.stabilityDuration
urn:ICSRr2:ProductInstance.stabilityTime
bridg:Epoch.description
description
bridg:Epoch.description
false
bridg:Epoch.description
The textual representation of the epoch.
bridg:Epoch.description
"A 2-week period during which eligibility is determined and baseline measurements are taken".
bridg:Epoch.description
"The first treatment epoch is a one-week period during which a single dose of one of the three investigational treatments is administered".
bridg:Epoch.description
urn:C3PR:PlannedEpoch.description
bridg:Epoch.description
urn:C3PR:Epoch.descriptionText
bridg:Epoch.description
urn:C3PRv2.9:Epoch.descriptionText
bridg:Epoch.description
urn:CTRv1.0:Epoch.description
bridg:Epoch.description
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component1/epoch.text
bridg:Epoch.description
urn:HL7SD:Epoch.text
bridg:Epoch.description
urn:TDM:StudyDesignEpoch.description
bridg:Epoch.description
urn:caAERSv2.2:Epoch.description
bridg:Epoch.name
name
bridg:Epoch.name
false
bridg:Epoch.name
A non-unique textual identifier for the epoch.
bridg:Epoch.name
first treatment epoch
bridg:Epoch.name
second treatment epoch
bridg:Epoch.name
first wash-out epoch
bridg:Epoch.name
second wash-out epoch
bridg:Epoch.name
When multiple Epochs have the same purpose (e.g., treatment), then the titles will probably include order numbers to distinguish them.
bridg:Epoch.name
urn:C3PR:Epoch.name
bridg:Epoch.name
urn:C3PR:PlannedEpoch.name
bridg:Epoch.name
urn:C3PRv2.9:Epoch.name
bridg:Epoch.name
urn:CDASHv1.1:DS.DSNEXT
bridg:Epoch.name
urn:CDASHv1.1:DS.EPOCH
bridg:Epoch.name
urn:CTOM:StudyTimePoint.epochName
bridg:Epoch.name
urn:CTRPv3.8:Epoch.name
bridg:Epoch.name
urn:CTRv1.0:Epoch.name
bridg:Epoch.name
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component1/epoch.title
bridg:Epoch.name
urn:HL7SD:Epoch.title
bridg:Epoch.name
urn:PSC:Period.name
bridg:Epoch.name
urn:PSC:Epoch.name
bridg:Epoch.name
urn:PSCv2.6:Epoch.name
bridg:Epoch.name
urn:SDTM_IGv3.1.1:DS.EPOCH
bridg:Epoch.name
urn:SDTM_IGv3.1.1:TA.EPOCH
bridg:Epoch.name
urn:SDTM_IGv3.1.2:TA.EPOCH
bridg:Epoch.name
urn:SDTM_IGv3.1.2:EX.EPOCH
bridg:Epoch.name
urn:SDTM_IGv3.1.2:SE.EPOCH
bridg:Epoch.name
urn:SDTM_IGv3.1.2:DV.EPOCH
bridg:Epoch.name
urn:SDTM_IGv3.1.2:DS.EPOCH
bridg:Epoch.name
urn:TDM:StudyDesignEpoch.name
bridg:Epoch.name
urn:caAERSv2.2:Epoch.name
bridg:Epoch.sequenceNumber
sequenceNumber
bridg:Epoch.sequenceNumber
false
bridg:Epoch.sequenceNumber
An integer specifying the relative sequential or temporal ordering of this epoch among other similar epochs in a study.
bridg:Epoch.sequenceNumber
In a Study that has Screening
bridg:Epoch.sequenceNumber
Treatment and Follow-Up epochs
bridg:Epoch.sequenceNumber
the sequence number indicates which Epoch precedes the other.
bridg:Epoch.sequenceNumber
urn:C3PR:PlannedEpoch.firstEpochIndicator
bridg:Epoch.sequenceNumber
urn:C3PR:Epoch.epochOrder
bridg:Epoch.sequenceNumber
urn:C3PRv2.9:Epoch.epchOrder
bridg:Epoch.sequenceNumber
urn:CTRv1.0:Epoch.sequenceNumber
bridg:Epoch.sequenceNumber
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component1.sequenceNumber
bridg:Epoch.sequenceNumber
urn:HL7SD:Component2.sequenceNumber
bridg:Epoch.sequenceNumber
urn:TDM:StudyDesignEpoch.epochSequenceNumber
bridg:Epoch.sequenceNumber
urn:caAERSv2.2:Epoch.order
bridg:Epoch.targetAccrualNumberRange
targetAccrualNumberRange
bridg:Epoch.targetAccrualNumberRange
true
bridg:Epoch.targetAccrualNumberRange
An integer falling within minimum and maximum bounds that specifies how many study subjects to be accrued for the epoch.
bridg:Epoch.targetAccrualNumberRange
Derived from the summary of all arm accruals in that Epoch. This will be the same as the study level target accrual unless this study has parallel Epochs, in which case the summary will only count the accruals for arms in this Epoch.
bridg:Epoch.targetAccrualNumberRange
urn:C3PRv2.9:Epoch.accrualCeiling
bridg:Epoch.targetAccrualNumberRange
urn:CTRv1.0:Epoch.targetAccrualNumberRange
bridg:Epoch.typeCode
typeCode
bridg:Epoch.typeCode
false
bridg:Epoch.typeCode
A coded value specifying the kind of epoch.
bridg:Epoch.typeCode
screening
bridg:Epoch.typeCode
treatment
bridg:Epoch.typeCode
follow-up
bridg:Epoch.typeCode
urn:C3PR:PlannedEpoch.type
bridg:Epoch.typeCode
urn:C3PRv2.9:Epoch.treatmentIndicator
bridg:Epoch.typeCode
urn:CTRPv3.8:Epoch.typeCode
bridg:Epoch.typeCode
urn:CTRv1.0:Epoch.typeCode
bridg:EvaluatedActivityRelationship.probabilityCode
probabilityCode
bridg:EvaluatedActivityRelationship.probabilityCode
false
bridg:EvaluatedActivityRelationship.probabilityCode
A coded value specifying the likelihood of the identified cause of an adverse event.
bridg:EvaluatedActivityRelationship.probabilityCode
unrelated
bridg:EvaluatedActivityRelationship.probabilityCode
unlikely
bridg:EvaluatedActivityRelationship.probabilityCode
possible
bridg:EvaluatedActivityRelationship.probabilityCode
probable
bridg:EvaluatedActivityRelationship.probabilityCode
definite (for adverse events in respect to CTEP and FAET)
bridg:EvaluatedActivityRelationship.probabilityCode
related
bridg:EvaluatedActivityRelationship.probabilityCode
possibly related
bridg:EvaluatedActivityRelationship.probabilityCode
unlikely related
bridg:EvaluatedActivityRelationship.probabilityCode
not related (for adverse events in respect to SDTM & E2B)
bridg:EvaluatedActivityRelationship.probabilityCode
urn:CTRv1.0:EvaluatedActivityRelationship.probabilityCode
in IndividualCaseSafetyReport
bridg:EvaluatedActivityRelationship.probabilityCode
urn:ICSRr2:CausalityAssessment.value
bridg:EvaluatedActivityRelationship.probabilityCode
urn:NCI_CRF_Standard:CDE_1285v3.0:_CTC_Adverse_Event_Attribution_Scale
bridg:EvaluatedActivityRelationship.probabilityCode
urn:caAERSv2.2:AdverseEventAttribution.attribution
bridg:EvaluatedActivityRelationship.probabilityCode
urn:caAERSv2.2:AdverseEvent.attributionToStudy
bridg:EvaluatedActivityRelationship.probabilityPercent
probabilityPercent
bridg:EvaluatedActivityRelationship.probabilityPercent
false
bridg:EvaluatedActivityRelationship.probabilityPercent
A number representing the likelihood of the identified cause of an adverse event.
bridg:EvaluatedActivityRelationship.probabilityPercent
60% likelihood that an adverse event was caused by an activity that was performed on the subject or study subject.
bridg:EvaluatedActivityRelationship.probabilityPercent
urn:AE:CausalAssessment.probability
bridg:EvaluatedActivityRelationship.probabilityPercent
urn:CTRv1.0:EvaluatedActivityRelationship.probabilityPercent
bridg:EvaluatedActivityRelationship.uncertaintyCode
uncertaintyCode
bridg:EvaluatedActivityRelationship.uncertaintyCode
false
bridg:EvaluatedActivityRelationship.uncertaintyCode
A coded value specifying whether and to what degree this evaluation or observation has been asserted to be in doubt in any way.
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:AE:CausalAssessment.certaintyCode
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:CDASHv1.1:AE.AEREL
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:CTOM:AdverseEvent.ctcAttributionCode
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:CTOM:AdverseEvent.ctcAttributionCodeSystem
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:CTRv1.0:EvaluatedActivityRelationship.uncertaintyCode
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:SDTM_IGv3.1.2:AE.AERELNST
bridg:EvaluatedActivityRelationship.uncertaintyCode
urn:SDTM_IGv3.1.2:AE.AEREL
bridg:EvaluatedResultRelationship.probabilityCode
probabilityCode
bridg:EvaluatedResultRelationship.probabilityCode
false
bridg:EvaluatedResultRelationship.probabilityCode
A coded value specifying the likelihood of the identified cause of an adverse event.
bridg:EvaluatedResultRelationship.probabilityCode
unrelated
bridg:EvaluatedResultRelationship.probabilityCode
unlikely
bridg:EvaluatedResultRelationship.probabilityCode
possible
bridg:EvaluatedResultRelationship.probabilityCode
probable
bridg:EvaluatedResultRelationship.probabilityCode
definite (for adverse events in respect to CTEP and FAET)
bridg:EvaluatedResultRelationship.probabilityCode
related
bridg:EvaluatedResultRelationship.probabilityCode
possibly related
bridg:EvaluatedResultRelationship.probabilityCode
unlikely related
bridg:EvaluatedResultRelationship.probabilityCode
not related (for adverse events in respect to SDTM & E2B)
bridg:EvaluatedResultRelationship.probabilityCode
urn:CTRv1.0:EvaluatedResultRelationship.probabilityCode
bridg:EvaluatedResultRelationship.probabilityCode
urn:NCI_CRF_Standard:CDE_1285v3.0:_CTC_Adverse_Event_Attribution_Scale
bridg:EvaluatedResultRelationship.probabilityCode
urn:caAERSv2.2:AdverseEventAttribution.attribution
bridg:EvaluatedResultRelationship.probabilityPercent
probabilityPercent
bridg:EvaluatedResultRelationship.probabilityPercent
false
bridg:EvaluatedResultRelationship.probabilityPercent
A number representing the likelihood of the identified cause of an adverse event.
bridg:EvaluatedResultRelationship.probabilityPercent
60% likelihood that an adverse event was caused by the evaluated result of diabetes.
bridg:EvaluatedResultRelationship.probabilityPercent
urn:AE:CausalAssessment.probability
bridg:EvaluatedResultRelationship.probabilityPercent
urn:CTRv1.0:EvaluatedResultRelationship.probabilityPercent
bridg:EvaluatedResultRelationship.uncertaintyCode
uncertaintyCode
bridg:EvaluatedResultRelationship.uncertaintyCode
false
bridg:EvaluatedResultRelationship.uncertaintyCode
A coded value specifying whether and to what degree this evaluation or observation has been asserted to be in doubt in any way.
bridg:EvaluatedResultRelationship.uncertaintyCode
urn:AE:CausalAssessment.certaintyCode
bridg:EvaluatedResultRelationship.uncertaintyCode
urn:CTRv1.0:EvaluatedResultRelationship.uncertaintyCode
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
interventionDescription
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
false
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
A character string that provides the key details of the intervention.
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
Interventions involving drugs may include dosage form
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
dosage
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
frequency and duration. (50 mg/m2
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
IV (in the vein) on day 5 of each 28 day cycle. Number of Cycles: until progression or unacceptable toxicity develops.)
bridg:ExpandedAccessStudyProtocolVersion.interventionDescription
urn:CTRv1.0:ExpandedAccessStudyProtocolVersion.interventionDescription
bridg:ExperimentalUnit.identifier
identifier
bridg:ExperimentalUnit.identifier
false
bridg:ExperimentalUnit.identifier
A unique symbol that establishes identity of the experimental unit.
bridg:ExperimentalUnit.identifier
patient number 7 on a study
bridg:ExperimentalUnit.identifier
urn:CTRv1.0:ExperimentalUnit.identifier
bridg:ExperimentalUnit.identifier
urn:HL7SP:ExperimentalUnit.id
bridg:ExperimentalUnit.statusCode
statusCode
bridg:ExperimentalUnit.statusCode
false
bridg:ExperimentalUnit.statusCode
A coded value specifying the phase in the lifecycle of the experimental unit.
bridg:ExperimentalUnit.statusCode
active
bridg:ExperimentalUnit.statusCode
cancelled
bridg:ExperimentalUnit.statusCode
pending
bridg:ExperimentalUnit.statusCode
suspended
bridg:ExperimentalUnit.statusCode
terminated
bridg:ExperimentalUnit.statusCode
nullified
bridg:ExperimentalUnit.statusCode
Please refer to the HL7 Role Status state transition diagram for further details.
bridg:ExperimentalUnit.statusCode
urn:CTRv1.0:ExperimentalUnit.statusCode
bridg:ExperimentalUnit.statusCode
urn:HL7SP:ExperimentalUnit.statusCode
bridg:ExperimentalUnit.statusDate
statusDate
bridg:ExperimentalUnit.statusDate
false
bridg:ExperimentalUnit.statusDate
The date (and time) on which the status is assigned to the experimental unit.
bridg:ExperimentalUnit.statusDate
urn:CTRv1.0:ExperimentalUnit.statusDate
bridg:ExperimentalUnit.statusDate
urn:HL7SP:ExperimentalUnit.effectiveTime
bridg:ExperimentalUnit.subgroupCode
subgroupCode
bridg:ExperimentalUnit.subgroupCode
false
bridg:ExperimentalUnit.subgroupCode
A coded value specifying the identification of uniform groups of experimental units for separate analysis or treatment.
bridg:ExperimentalUnit.subgroupCode
Clinical Data Update System (CDUS) Reporting (for the National Cancer Institute (NCI)
bridg:ExperimentalUnit.subgroupCode
urn:C3PR:StudySubject.subgroup
bridg:ExperimentalUnit.subgroupCode
urn:CTOM:StudyParticipantAssignment.subgroupCode
bridg:ExperimentalUnit.subgroupCode
urn:CTRv1.0:ExperimentalUnit.subgroupCode
bridg:ExperimentalUnit.subgroupCode
urn:NCI_CRF_Standard:CDE_1925v2.31:_Patient_Subgroup_Code
bridg:FoodProduct.stabilityDuration
stabilityDuration
bridg:FoodProduct.stabilityDuration
false
bridg:FoodProduct.stabilityDuration
The period of time during which the food product is considered usable after it is activated (opened).
bridg:FoodProduct.stabilityDuration
urn:CTRv1.0:FoodProduct.stabilityDuration
in R_Product
bridg:FoodProduct.stabilityDuration
urn:ICSRr2:ProductInstance.stabilityTime
bridg:GeneralStatisticalConsideration.text
text
bridg:GeneralStatisticalConsideration.text
false
bridg:GeneralStatisticalConsideration.text
Textual or media-based representation of the general statistical consideration.
bridg:GeneralStatisticalConsideration.text
Centers within a region with fewer than 3 subjects will be grouped into a pooled center for the region.
bridg:GeneralStatisticalConsideration.text
Visits will be assigned to assessment windows defined by +/- 7 days from the target visit date as defined in the Time and Events Schedule. If multiple visits fall within an assessment window
bridg:GeneralStatisticalConsideration.text
the visit closest to the target date will be used. In the case of a tie
bridg:GeneralStatisticalConsideration.text
the earliest visit date will be used.
bridg:GeneralStatisticalConsideration.text
urn:Statistics_v1.0:GeneralStatisticalConsideration.text
bridg:GeneralStatisticalConsideration.typeCode
typeCode
bridg:GeneralStatisticalConsideration.typeCode
false
bridg:GeneralStatisticalConsideration.typeCode
A coded value specifying the kind of general statistical consideration.
bridg:GeneralStatisticalConsideration.typeCode
subgroup
bridg:GeneralStatisticalConsideration.typeCode
analysis set
bridg:GeneralStatisticalConsideration.typeCode
missing data algorithm
bridg:GeneralStatisticalConsideration.typeCode
derivation algorithm
bridg:GeneralStatisticalConsideration.typeCode
assessment window
bridg:GeneralStatisticalConsideration.typeCode
multiple comparison strategy
bridg:GeneralStatisticalConsideration.typeCode
center pooling
bridg:GeneralStatisticalConsideration.typeCode
urn:Statistics_v1.0:GeneralStatisticalConsideration.typeCode
bridg:GovernmentFunding.fundingCategoryCode
fundingCategoryCode
bridg:GovernmentFunding.fundingCategoryCode
false
bridg:GovernmentFunding.fundingCategoryCode
A coded value specifying the type of funding provided for a study.
bridg:GovernmentFunding.fundingCategoryCode
National
bridg:GovernmentFunding.fundingCategoryCode
Externally Peer-Reviewed
bridg:GovernmentFunding.fundingCategoryCode
Institutional
bridg:GovernmentFunding.fundingCategoryCode
Industrial
bridg:GovernmentFunding.fundingCategoryCode
This is as defined for the NCI Summary 4 Funding requirements.
bridg:GovernmentFunding.fundingCategoryCode
urn:CTRPv3.8:StudyResourcing.typeCode
bridg:GovernmentFunding.fundingCategoryCode
urn:HSDBv1.0:[Summary_4_Funder].Summary_4_Funding_Category
bridg:GovernmentFunding.fundingMechanismCode
fundingMechanismCode
bridg:GovernmentFunding.fundingMechanismCode
false
bridg:GovernmentFunding.fundingMechanismCode
A coded value specifying the unique identifier for areas of extramural research activity applied to various funding mechanisms.
bridg:GovernmentFunding.fundingMechanismCode
R01 (Research Project)
bridg:GovernmentFunding.fundingMechanismCode
U10 (Cooperative Clinical Research Cooperative Agreements)
bridg:GovernmentFunding.fundingMechanismCode
urn:CTRPv1.0:StudyResourcing.fundingMechanismCode
bridg:GovernmentFunding.fundingMechanismCode
urn:CTRPv1.0:ResearchOrganization.fundingMechanism
bridg:GovernmentFunding.fundingMechanismCode
urn:CTRPv3.8:ResearchOrganization.fundingMechanism
bridg:GovernmentFunding.fundingMechanismCode
urn:CTRPv3.8:StudyResourcing.fundingMechanismCode
bridg:GovernmentFunding.fundingMechanismCode
urn:HSDBv1.0:[NIH_Grant].Funding_Mechanism
bridg:GovernmentFunding.nciProgramCode
nciProgramCode
bridg:GovernmentFunding.nciProgramCode
false
bridg:GovernmentFunding.nciProgramCode
A coded value specifying the organizational units within the National Cancer Insitute (NCI) (divisions, programs and offices) that provide funding.
bridg:GovernmentFunding.nciProgramCode
CTEP (Cancer Therapy Evaluation Program)
bridg:GovernmentFunding.nciProgramCode
DTP (Developmental Therapeutics Program)
bridg:GovernmentFunding.nciProgramCode
CDP (Cancer Diagnosis Program)
bridg:GovernmentFunding.nciProgramCode
urn:CTRPv3.8:StudyResourcing.nciDivisionProgramCode
bridg:GovernmentFunding.nciProgramCode
urn:HSDBv1.0:[NIH_Grant].NCI_Division/Program_Code
bridg:GovernmentFunding.nihInstituteCode
nihInstituteCode
bridg:GovernmentFunding.nihInstituteCode
false
bridg:GovernmentFunding.nihInstituteCode
A two letter coded value specifying the first major-level subdivision of the organization that supports a grant, contract, or inter-agency agreement. The support may be financial or administrative.
bridg:GovernmentFunding.nihInstituteCode
CP2 Division of Cancer Epidemiology and Genetics (NCI)
bridg:GovernmentFunding.nihInstituteCode
LM National Library of Medicine (NLM)
bridg:GovernmentFunding.nihInstituteCode
urn:CTRPv1.0:StudyResourcing.nihInstituteCode
bridg:GovernmentFunding.nihInstituteCode
urn:CTRPv3.8:StudyResourcing.nihInstituteCode
bridg:GovernmentFunding.nihInstituteCode
urn:HSDBv1.0:[NIH_Grant].Institute_Code
bridg:GovernmentFunding.serialNumberText
serialNumberText
bridg:GovernmentFunding.serialNumberText
false
bridg:GovernmentFunding.serialNumberText
A character string that represents the six-digit number generally assigned sequentially to a funding mechanism within an institute, center, or division.
bridg:GovernmentFunding.serialNumberText
urn:CTRPv1.0:StudyResourcing.serialNumber
bridg:GovernmentFunding.serialNumberText
urn:CTRPv3.8:StudyResourcing.serialNumber
bridg:GovernmentFunding.serialNumberText
urn:HSDBv1.0:[NIH_Grant].Serial_Number
bridg:GovernmentFunding.typeCode
typeCode
bridg:GovernmentFunding.typeCode
false
bridg:GovernmentFunding.typeCode
A coded value specifying the kind of application received and processed.
bridg:GovernmentFunding.typeCode
Type 5 (Noncompeting Grant Progress Report)
bridg:GovernmentFunding.typeCode
Type 1 (New)
bridg:GovernmentFunding.typeCode
urn:CTRPv1.0:StudyResourcing.grantTypeCode
bridg:GovernmentFunding.typeCode
urn:CTRPv1.0:StudyResourcing.fundingTypeCode
bridg:HealthcareFacility.effectiveDateRange
effectiveDateRange
bridg:HealthcareFacility.effectiveDateRange
false
bridg:HealthcareFacility.effectiveDateRange
The date (and time) span for when the healthcare facility is active.
bridg:HealthcareFacility.effectiveDateRange
urn:C3PR:HealthCareSite.startDate
bridg:HealthcareFacility.effectiveDateRange
urn:CTOM:HealthcareSite.statusDate
bridg:HealthcareFacility.effectiveDateRange
urn:CTOM:HealthcareSite.statusCode
bridg:HealthcareFacility.effectiveDateRange
urn:CTRPv1.0:HealthCareFacility.statusDateRange
bridg:HealthcareFacility.effectiveDateRange
urn:CTRPv1.0:HealthCareFacility.statusCode
bridg:HealthcareFacility.effectiveDateRange
urn:CTRv1.0:HealthcareFacility.effectiveDateRange
bridg:HealthcareFacility.identifier
identifier
bridg:HealthcareFacility.identifier
false
bridg:HealthcareFacility.identifier
A unique symbol that establishes identity of the healthcare facility.
bridg:HealthcareFacility.identifier
In Cancer Therapy Evaluation Program (CTEP)
bridg:HealthcareFacility.identifier
every site that interacts with the National Cancer Institute (NCI) gets an NCI unique identifier.
bridg:HealthcareFacility.identifier
Hospitals get an American Hospital Association (AHA) ID.
bridg:HealthcareFacility.identifier
urn:C3PR:HealthCareSite.identifier
bridg:HealthcareFacility.identifier
urn:CTOM:HealthcareSite.nciInstituteCode
bridg:HealthcareFacility.identifier
urn:CTRPv1.0:HealthCareFacility.identifier
bridg:HealthcareFacility.identifier
urn:CTRv1.0:HealthcareFacility.identifier
bridg:HealthcareFacility.identifier
urn:Lab:HealthCareSite.identifier
bridg:HealthcareFacility.identifier
urn:LabViewer2.2:HealthcareSite.nciInstituteCode
bridg:HealthcareFacility.identifier
urn:NCI_CRF_Standard:CDE_2003307v4.0:_Registering_Institution_Identification_Code
bridg:HealthcareFacility.identifier
urn:NCI_CRF_Standard:CDE_2481533V1.0:_Treating_Institution_Identifier_Code
bridg:HealthcareFacility.postalAddress
postalAddress
bridg:HealthcareFacility.postalAddress
false
bridg:HealthcareFacility.postalAddress
A contact point used to send physical forms of communication to the healthcare facility.
bridg:HealthcareFacility.postalAddress
urn:C3PR:HealthCareSite.postalAddress
bridg:HealthcareFacility.postalAddress
urn:CTOM:HealthcareSite.postalCode
bridg:HealthcareFacility.postalAddress
urn:CTOM:HealthcareSite.stateCode
bridg:HealthcareFacility.postalAddress
urn:CTOM:HealthcareSite.city
bridg:HealthcareFacility.postalAddress
urn:CTOM:HealthcareSite.countryCode
bridg:HealthcareFacility.postalAddress
urn:CTRPv3.8:HealthCareFacility.postalAddress
bridg:HealthcareFacility.postalAddress
urn:CTRv1.0:HealthcareFacility.postalAddress
bridg:HealthcareFacility.postalAddress
urn:LabViewer2.2:HealthcareSite.streetAddress
bridg:HealthcareFacility.postalAddress
urn:LabViewer2.2:HealthcareSite.stateCode
bridg:HealthcareFacility.postalAddress
urn:LabViewer2.2:HealthcareSite.city
bridg:HealthcareFacility.postalAddress
urn:LabViewer2.2:HealthcareSite.countryCode
bridg:HealthcareFacility.postalAddress
urn:LabViewer2.2:HealthcareSite.postalCode
bridg:HealthcareFacility.telecomAddress
telecomAddress
bridg:HealthcareFacility.telecomAddress
false
bridg:HealthcareFacility.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the healthcare facility.
bridg:HealthcareFacility.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:HealthcareFacility.telecomAddress
urn:CTRPv3.8:HealthCareFacility.telecomAddress
bridg:HealthcareFacility.telecomAddress
urn:CTRv1.0:HealthcareFacility.telecomAddress
bridg:HealthcareFacility.telecomAddress
urn:LabViewer2.2:HealthcareSite.telecomAddress
bridg:HealthcareProvider.effectiveDateRange
effectiveDateRange
bridg:HealthcareProvider.effectiveDateRange
false
bridg:HealthcareProvider.effectiveDateRange
The date (and time) span for when the healthcare provider is active.
bridg:HealthcareProvider.effectiveDateRange
urn:C3PRv2.9:HealthcareSiteInvestigator.statusDate
bridg:HealthcareProvider.effectiveDateRange
urn:CTRPv1.0:HealthCareProvider.statusDateRange
bridg:HealthcareProvider.effectiveDateRange
urn:CTRPv1.0:HealthCareProvider.statusCode
bridg:HealthcareProvider.effectiveDateRange
urn:CTRv1.0:HealthcareProvider.effectiveDateRange
bridg:HealthcareProvider.effectiveDateRange
urn:caAERSv2.2:SiteInvestigator.statusDate
bridg:HealthcareProvider.effectiveDateRange
urn:caAERSv2.2:SiteInvestigator.statusCode
bridg:HealthcareProvider.identifier
identifier
bridg:HealthcareProvider.identifier
false
bridg:HealthcareProvider.identifier
A unique symbol that establishes identity of the healthcare provider.
bridg:HealthcareProvider.identifier
urn:C3PRv2.9:RemoteInvestigator.externalId
bridg:HealthcareProvider.identifier
urn:CTOM:Investigator.nciIdentifier
bridg:HealthcareProvider.identifier
urn:CTRPv1.0:HealthCareProvider.identifier
bridg:HealthcareProvider.identifier
urn:CTRv1.0:HealthcareProvider.identifier
bridg:HealthcareProvider.identifier
urn:FDA_HL7_SD_SD_DSTU2012:assignedEntity.id
bridg:HealthcareProvider.identifier
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/performer/assignedEntity.id
bridg:HealthcareProvider.identifier
urn:Lab:Investigator.identifier
bridg:HealthcareProvider.identifier
urn:caAERSv2.2:Investigator.nciIdentifier
bridg:HealthcareProvider.postalAddress
postalAddress
bridg:HealthcareProvider.postalAddress
false
bridg:HealthcareProvider.postalAddress
A contact point used to send physical forms of communication to the healthcare provider.
bridg:HealthcareProvider.postalAddress
urn:CTRPv1.0:HealthCareProvider.postalAddress
bridg:HealthcareProvider.postalAddress
urn:CTRv1.0:HealthcareProvider.postalAddress
bridg:HealthcareProvider.postalAddress
urn:FDA_HL7_SD_SD_DSTU2012:assignedEntity.addr
bridg:HealthcareProvider.postalAddress
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/performer/assignedEntity.addr
in IndividualCaseSafetyReport
bridg:HealthcareProvider.postalAddress
urn:ICSRr2:AssignedEntity.addr
bridg:HealthcareProvider.postalAddress
urn:LabViewer2.2:Investigator.postalCode
bridg:HealthcareProvider.postalAddress
urn:LabViewer2.2:Investigator.city
bridg:HealthcareProvider.postalAddress
urn:LabViewer2.2:Investigator.state
bridg:HealthcareProvider.postalAddress
urn:LabViewer2.2:Investigator.countryCode
bridg:HealthcareProvider.postalAddress
urn:LabViewer2.2:Investigator.streetAddress
bridg:HealthcareProvider.telecomAddress
telecomAddress
bridg:HealthcareProvider.telecomAddress
false
bridg:HealthcareProvider.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the healthcare provider.
bridg:HealthcareProvider.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:HealthcareProvider.telecomAddress
urn:CTRPv1.0:HealthCareProvider.telecomAddress
bridg:HealthcareProvider.telecomAddress
urn:CTRv1.0:HealthcareProvider.telecomAddress
bridg:HealthcareProvider.telecomAddress
urn:FDA_HL7_SD_SD_DSTU2012:assignedEntity.telecom
bridg:HealthcareProvider.telecomAddress
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/performer/assignedEntity.telecom
in IndividualCaseSafetyReport
bridg:HealthcareProvider.telecomAddress
urn:ICSRr2:AssignedEntity.telecom
bridg:HealthcareProvider.telecomAddress
urn:LabViewer2.2:Investigator.telecomAddress
bridg:HealthcareProvider.telecomAddress
urn:LabViewer2.2:Investigator.phone
bridg:HealthcareProvider.telecomAddress
urn:caAERSv2.2:PersonContact.ReportPerson.Reporter.contactMechanisms
bridg:HealthcareProvider.telecomAddress
urn:caAERSv2.2:Investigator.faxNumber
bridg:HealthcareProvider.telecomAddress
urn:caAERSv2.2:SiteInvestigator.emailAddress
bridg:HealthcareProvider.telecomAddress
urn:caAERSv2.2:PersonContact.ReportPerson.Physician.contactMechanisms
bridg:HealthcareProvider.telecomAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:HealthcareProvider.telecomAddress
urn:caAERSv2.2:Investigator.phoneNumber
bridg:HealthcareProviderGroup.effectiveDateRange
effectiveDateRange
bridg:HealthcareProviderGroup.effectiveDateRange
false
bridg:HealthcareProviderGroup.effectiveDateRange
The date (and time) span for when the healthcare provider group is active.
bridg:HealthcareProviderGroup.effectiveDateRange
urn:C3PR:InvestigatorGroup.endDate
bridg:HealthcareProviderGroup.effectiveDateRange
urn:C3PR:InvestigatorGroup.startDate
bridg:HealthcareProviderGroup.effectiveDateRange
urn:C3PRv2.9:InvestigatorGroup.endDate
bridg:HealthcareProviderGroup.effectiveDateRange
urn:C3PRv2.9:InvestigatorGroup.startDate
bridg:HealthcareProviderGroupMember.effectiveDateRange
effectiveDateRange
bridg:HealthcareProviderGroupMember.effectiveDateRange
false
bridg:HealthcareProviderGroupMember.effectiveDateRange
The date (and time) span for when the healthcare provider group member is active.
bridg:HealthcareProviderGroupMember.effectiveDateRange
urn:C3PR:SiteInvestigatorGroupAffiliation.endDate
bridg:HealthcareProviderGroupMember.effectiveDateRange
urn:C3PR:SiteInvestigatorGroupAffiliation.startDate
bridg:HealthcareProviderGroupMember.effectiveDateRange
urn:C3PRv2.9:SiteInvestigatorGroupAffiliation.endDate
bridg:HealthcareProviderGroupMember.effectiveDateRange
urn:C3PRv2.9:SiteInvestigatorGroupAffiliation.startDate
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
acceptsHealthyVolunteersIndicator
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
false
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
Specifies whether persons who have not had the condition(s) being studied or otherwise related conditions or symptoms, as specified in the eligibility requirements, may participate in the study.
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
urn:CTGOV:Accepts_Healthy_Volunteers?
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
urn:CTOM:Accepts_healthty_volunteers
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
urn:CTRPv1.0:InterventionalStudyProtocol.acceptsHealthyVolunteersIndicator
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
urn:CTRPv3.8:StudyProtocol.acceptsHealthyVolunteersIndicator
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
urn:CTRRr3:InterventionalStudy.acceptsHealthyVolunteersIndicator
bridg:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
urn:CTRv1.0:InterventionalStudyProtocolVersion.acceptsHealthyVolunteersIndicator
bridg:InterventionalStudyProtocolVersion.allocationCode
allocationCode
bridg:InterventionalStudyProtocolVersion.allocationCode
false
bridg:InterventionalStudyProtocolVersion.allocationCode
A coded value specifying the method of assigning experimental units to treatment or control groups.
bridg:InterventionalStudyProtocolVersion.allocationCode
n/a
bridg:InterventionalStudyProtocolVersion.allocationCode
randomized controlled study
bridg:InterventionalStudyProtocolVersion.allocationCode
non-randomized study
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTGOV:Study_Design_Allocation
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTOM:Protocol.randomizedIndicator
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTRPv1.0:InterventionalStudyProtocol.allocationCode
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTRPv3.8:InterventionalStudyProtocol.allocationCode
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTRR:Randomization
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTRRr3:InterventionalStudy.allocationCode
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:CTRv1.0:InterventionalStudyProtocolVersion.allocationCode
bridg:InterventionalStudyProtocolVersion.allocationCode
urn:SDTM_IGv3.1.2:TSVAL_where_TSPARMCD_RANDOM
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
blindedRoleCode
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
false
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
A coded value specifying the roles of individuals who are masked for single or double blind studies.
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
subject
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
caregiver
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
investigator
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
outcomes assessor
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:CTGOV:Masking_Role
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:CTRPv1.0:InterventionalStudyProtocol.blindedRoleCode
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:CTRPv3.8:InterventionalStudyProtocol.blindedRoleCode
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:CTRR:Blinded_Roles
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:CTRRr3:InterventionalStudy.blindedRoleCode
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:CTRv1.0:InterventionalStudyProtocolVersion.blindedRoleCode
bridg:InterventionalStudyProtocolVersion.blindedRoleCode
urn:WHO:Study_Type_Masking_Who_is_Blinded
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
blindingSchemaCode
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
false
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
A coded value specifying the type of masking used on a study protocol to ensure that the results are not biased by the study subjects or investigators.
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
Double-blinded would indicate that both the investigator and the study subject would not know whether the intervention was a placebo or an active therapeutic intervention.
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
Open Label
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
Double Blind
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
Single Blind
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:C3PR:Study.blindedIndicator
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTGOV:Study_Design_Masking
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTOM:Protocol.blindedIndicator
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTR_Rr2:Trial_design_Double_blind
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTR_Rr2:Trial_design_Parallel_group
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTR_Rr2:Trial_design_Single_blind
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTRPv1.0:InterventionalStudyProtocol.blindingSchemaCode
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTRPv3.8:InterventionalStudyProtocol.blindingSchemaCode
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTRR:Blinding_Design
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTRRr3:InterventionalStudy.blindingSchemaCode
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:CTRv1.0:InterventionalStudyProtocolVersion.blindingSchemaCode
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:SDTM_IGv3.1.2:TSVAL_where_TSPARMCD_TBLIND
bridg:InterventionalStudyProtocolVersion.blindingSchemaCode
urn:WHO:Masking
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
controlConcurrencyTypeCode
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
false
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
A coded value specifying the temporal relationships of the control to the study intervention.
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
concurrent
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
historical
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
pre/post (patient owned control)
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
urn:CTRPv1.0:InterventionalStudyProtocol.controlConcurrencyType
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
urn:CTRR:Concurrency
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
urn:CTRRr3:InterventionalStudy.controlConcurrencyTypeCode
bridg:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
urn:CTRv1.0:InterventionalStudyProtocolVersion.controlConcurrencyTypeCode
bridg:InterventionalStudyProtocolVersion.controlTypeCode
controlTypeCode
bridg:InterventionalStudyProtocolVersion.controlTypeCode
false
bridg:InterventionalStudyProtocolVersion.controlTypeCode
A coded value specifying the kind of comparison or comparator against which the study treatment is evaluated.
bridg:InterventionalStudyProtocolVersion.controlTypeCode
placebo
bridg:InterventionalStudyProtocolVersion.controlTypeCode
active
bridg:InterventionalStudyProtocolVersion.controlTypeCode
historical
bridg:InterventionalStudyProtocolVersion.controlTypeCode
uncontrolled
bridg:InterventionalStudyProtocolVersion.controlTypeCode
dose comparison
bridg:InterventionalStudyProtocolVersion.controlTypeCode
urn:CTRPv1.0:InterventionalStudyProtocol.controlType
bridg:InterventionalStudyProtocolVersion.controlTypeCode
urn:CTRR:Control
bridg:InterventionalStudyProtocolVersion.controlTypeCode
urn:CTRRr3:InterventionalStudy.controlTypeCode
bridg:InterventionalStudyProtocolVersion.controlTypeCode
urn:CTRv1.0:InterventionalStudyProtocolVersion.controlTypeCode
bridg:InterventionalStudyProtocolVersion.controlTypeCode
urn:SDTM_IGv3.1.2:TSVAL_where_TSPARMCD_TCNTRL
bridg:InterventionalStudyProtocolVersion.dataMonitoringCommitteeIndicator
dataMonitoringCommitteeIndicator
bridg:InterventionalStudyProtocolVersion.dataMonitoringCommitteeIndicator
true
bridg:InterventionalStudyProtocolVersion.dataMonitoringCommitteeIndicator
Specifies whether a data monitoring committee is appointed to the study.
bridg:InterventionalStudyProtocolVersion.dataMonitoringCommitteeIndicator
Derived from the existence of an association between StudyProtocolVersion and
StudyOversightAuthority where the associated OversightCommittee.typeCode= "data monitoring committee".
bridg:InterventionalStudyProtocolVersion.dataMonitoringCommitteeIndicator
urn:CTRPv3.8:StudyProtocol.dataMonitoringCommitteeAppointedIndicator
bridg:InterventionalStudyProtocolVersion.dataMonitoringCommitteeIndicator
urn:CTRRr3:Study.dataMonitoringCommitteeIndicator
bridg:InterventionalStudyProtocolVersion.interventionDescription
interventionDescription
bridg:InterventionalStudyProtocolVersion.interventionDescription
false
bridg:InterventionalStudyProtocolVersion.interventionDescription
A character string that provides the key details of the intervention.
bridg:InterventionalStudyProtocolVersion.interventionDescription
The details may distinguish between arms of a study (e.g.
bridg:InterventionalStudyProtocolVersion.interventionDescription
comparison of different dosages of drug) and/or among similar interventions (e.g.
bridg:InterventionalStudyProtocolVersion.interventionDescription
comparison of multiple implantable cardiac defibrillators).
bridg:InterventionalStudyProtocolVersion.interventionDescription
Interventions involving drugs may include dosage form
bridg:InterventionalStudyProtocolVersion.interventionDescription
dosage
bridg:InterventionalStudyProtocolVersion.interventionDescription
frequency and duration. (50 mg/m2
bridg:InterventionalStudyProtocolVersion.interventionDescription
IV (in the vein) on day 5 of each 28 day cycle. Number of Cycles: until progression or unacceptable toxicity develops.)
bridg:InterventionalStudyProtocolVersion.interventionDescription
urn:CTGOV:Intervention_Description
bridg:InterventionalStudyProtocolVersion.interventionDescription
urn:CTRPv1.0:InterventionalStudyProtocol.primaryPurposeCode
bridg:InterventionalStudyProtocolVersion.interventionDescription
urn:CTRR:Description_of_investigational_treatments
bridg:InterventionalStudyProtocolVersion.interventionDescription
urn:CTRR:Intervention_Description
bridg:InterventionalStudyProtocolVersion.interventionDescription
urn:CTRRr3:InterventionalStudy.interventionDescription
bridg:InterventionalStudyProtocolVersion.interventionDescription
urn:CTRv1.0:InterventionalStudyProtocolVersion.interventionDescription
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
interventionGroupQuantity
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
false
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
An integer specifying the number of intervention groups.
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
Enter 1 for single-arm study.
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
Number of Arms
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
This attribute is potentially derivable once the study design has been defined.
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
urn:CTGOV:Number_of_Arms
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
urn:CTRPv1.0:InterventionalStudyProtocol.numberOfInterventionGroups
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
urn:CTRPv3.8:InterventionalStudyProtocol.numberOfInterventionGroups
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
urn:CTRR:Number_of_Arms
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
urn:CTRRr3:InterventionalStudy.interventionGroupQuantity
bridg:InterventionalStudyProtocolVersion.interventionGroupQuantity
urn:CTRv1.0:InterventionalStudyProtocolVersion.interventionGroupQuantity
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
interventionTypeCode
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
false
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
A coded value specifying the kind of intervention being studied.
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
Drug
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
Radiation
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
Lifestyle
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
Relevant for categorization or when not conveying the details of the studied intervention.
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:CTRPv3.8:InterventionalStudyProtocol.interventionTypeCode
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:CTRRr3:PlannedIntervention.typeCode
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:CTRv1.0:InterventionalStudyProtocolVersion.interventionCategoryCode
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:NCI_CRF_Standard:CDE_2542520v1.0:_Prior_Therapy_Other_Administered_Specify
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:NCI_CRF_Standard:CDE_64208v3.0:_Therapy_Name_Type
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:NCI_CRF_Standard:CDE_65292v4.0:_Systemic_Therapy_Type_Specify
bridg:InterventionalStudyProtocolVersion.interventionTypeCode
urn:NCI_CRF_Standard:CDE_2008450v2.0:_Prior_Therapy_Administered_Type
bridg:InterventionalStudyProtocolVersion.studyAgentRandomizationFraction
studyAgentRandomizationFraction
bridg:InterventionalStudyProtocolVersion.studyAgentRandomizationFraction
false
bridg:InterventionalStudyProtocolVersion.studyAgentRandomizationFraction
A number representing the quantity of study subjects in the overall study who receive at least one study agent (as opposed to placebo) divided by the quantity of subjects in the study overall - independent of dosage or other protocol variations.
bridg:InterventionalStudyProtocolVersion.studyAgentRandomizationFraction
This value can be thought of as the percentage of study subjects who will be exposed to the study agent(s), though it is expressed as a real number with a maximum value of 1.0.
bridg:InterventionalStudyProtocolVersion.studyAgentRandomizationFraction
urn:CTRv1.0:InterventionalStudyProtocolVersion.randomizationQuotient
bridg:Laboratory.identifier
identifier
bridg:Laboratory.identifier
false
bridg:Laboratory.identifier
A unique symbol that establishes identity of the laboratory.
bridg:Laboratory.identifier
Clinical Laboratory Improvement Act/Amendment (CLIA) ID
bridg:Laboratory.identifier
urn:CTRv1.0:Laboratory.identifier
bridg:Laboratory.identifier
urn:HL7SP:Service_Provider.id
bridg:Laboratory.identifier
urn:Lab:PerformingLaboratory.identifier
bridg:Laboratory.identifier
urn:Lab:CentralLaboratory.identifier
bridg:Laboratory.identifier
urn:LabViewer2.2:CentralLaboratory.identifier
bridg:Laboratory.identifier
urn:LabViewer2.2:PerformingLaboratory.identifier
bridg:Material.actualIndicator
actualIndicator
bridg:Material.actualIndicator
false
bridg:Material.actualIndicator
Specifies whether the material is a particular instance (actual) vs. universal kind.
bridg:Material.actualIndicator
To indicate a particular Material
bridg:Material.actualIndicator
actualIndicator = "true". To indicate a kind of Material
bridg:Material.actualIndicator
actualIndicator = "false".
bridg:Material.actualIndicator
urn:CTRv1.0:Material.actualIndicator
choice box.determinerCode
bridg:Material.actualIndicator
urn:HL7SD:ExperimentalUnit_ExperimentalUnit2
Universal
bridg:Material.actualIndicator
urn:HL7SD:R_AssignedEntity
in R_Product
bridg:Material.actualIndicator
urn:ICSRr2:MaterialKind.determinerCode
in R_Product
bridg:Material.actualIndicator
urn:ICSRr2:Product.determinerCode
bridg:Material.code
code
bridg:Material.code
false
bridg:Material.code
A coded value specifying the non-unique textual identifier for the material.
bridg:Material.code
aspirin
bridg:Material.code
tobacco
bridg:Material.code
caffeine
bridg:Material.code
The granularity of the code may vary depending on the specificity of the material. For example, acetaminophen, Tylenol, Tylenol 250 mg gel cap.
bridg:Material.code
urn:CDASHv1.1:CM.CMINGRD
bridg:Material.code
urn:CTR_Rr2:Comparator_a_placebo
bridg:Material.code
urn:CTR_Rr2:EV_Identifiable_Product_Code
bridg:Material.code
urn:CTR_Rr2:Other_comparator
bridg:Material.code
urn:CTR_Rr2:AS_current_sponsor_code
bridg:Material.code
urn:CTR_Rr2:Tissue_Engineered_Other
bridg:Material.code
urn:CTR_Rr2:Comparator_another_MP
bridg:Material.code
urn:CTR_Rr2:Tissue_Engineered_type_differentiated
bridg:Material.code
urn:CTR_Rr2:Tissue_Engineered_type_stem
bridg:Material.code
urn:CTR_Rr2:Placebo_major_ingredients
EudraVigilance Substance Code
bridg:Material.code
urn:CTR_Rr2:EV
bridg:Material.code
urn:CTRPv1.0:Drug.nameCode
bridg:Material.code
urn:CTRPv1.0:SubstanceAdministration.treatmentVehicleCode
s product name(s
bridg:Material.code
urn:CTRR:Comparator
bridg:Material.code
urn:CTRR:Intervention_Name
bridg:Material.code
urn:CTRR:StudyAgent
bridg:Material.code
urn:CTRRr3:Product.nameCode
bridg:Material.code
urn:CTRv1.0:Material.code
bridg:Material.code
urn:FDA_HL7_SD_SD_DSTU2012:manufacturedMaterial.code
bridg:Material.code
urn:HCTv1.0:CDE_2739625:Preparative_Regimen.What_was_the_type_of_preparative_regimen_medication?
in R_Product
bridg:Material.code
urn:ICSRr2:MaterialKind.code
in R_Specimen universal
bridg:Material.code
urn:ICSRr2:ManufacturedMaterial.code
in R_Specimen universal
bridg:Material.code
urn:ICSRr2:Natural.code
bridg:Material.code
urn:LabViewer2.2:SpecimenMaterialType.codeSystemVersion
bridg:Material.code
urn:LabViewer2.2:SpecimenMaterialType.codeSystemName
bridg:Material.code
urn:LabViewer2.2:SpecimenMaterialType.displayName
bridg:Material.code
urn:LabViewer2.2:SpecimenMaterialType.codeSystem
bridg:Material.code
urn:LabViewer2.2:SpecimenMaterialType.code
bridg:Material.code
urn:NCI_CRF_Standard:CDE_2867247v1.0:_Agent_NCI_Enterprise_Vocabulary_Services_Code
bridg:Material.code
urn:SDTM_IGv3.1.1:CM.CMTRT
bridg:Material.code
urn:SDTM_IGv3.1.1:EX.EXTRTV
bridg:Material.code
urn:SDTM_IGv3.1.2:EX.EXTRTV
bridg:Material.code
urn:SDTM_IGv3.1.2:MB.MBSPEC
bridg:Material.code
urn:SDTM_IGv3.1.2:PC.PCSPEC
bridg:Material.code
urn:SDTM_IGv3.1.2:CM.CMDECOD
bridg:Material.code
urn:SDTM_IGv3.1.2:LB.LBSPEC
bridg:Material.code
urn:SDTM_IGv3.1.2:SU.SUDECOD
bridg:Material.code
urn:SDTM_IGv3.1.2:PP.PPSPEC
bridg:Material.code
urn:caAERSv2.2:StudyParticipantPreExistingCondition___PriorTherapy.meddraTerm
bridg:Material.code
urn:caAERSv2.2:StudyParticipantPreExistingCondition___PriorTherapy.text
bridg:Material.code
urn:caAERSv2.2:SAEReportPreExistingCondition___PriorTherapy.meddraCode
bridg:Material.code
urn:caAERSv2.2:SAEReportPreExistingCondition___PriorTherapy.text
bridg:Material.code
urn:caAERSv2.2:StudyParticipantPriorTherapy.other
bridg:Material.code
urn:caAERSv2.2:ChemoAgent.name
bridg:Material.code
urn:caAERSv2.2:StudyAgent.otherAgent
bridg:Material.code
urn:caAERSv2.2:SAEReportPriorTherapy.other
bridg:Material.code
urn:caAERSv2.2:SAEReportPreExistingCondition___PriorTherapy.meddraTerm
bridg:Material.code
urn:caAERSv2.2:StudyParticipantPreExistingCondition___PriorTherapy.meddraCode
bridg:Material.description
description
bridg:Material.description
false
bridg:Material.description
The textual representation of the material.
bridg:Material.description
urn:CTGOV:Biospecimen_Description
bridg:Material.description
urn:CTOM:Agent.descriptionText
bridg:Material.description
urn:CTR_Rr2:AS_description
bridg:Material.description
urn:CTR_Rr2:Tissue_Engineered_differentiated_specification
bridg:Material.description
urn:CTR_Rr2:Device_description
bridg:Material.description
urn:CTR_Rr2:Tissue_Engineered_Other_specification
bridg:Material.description
urn:CTR_Rr2:Device_Other_specification
bridg:Material.description
urn:CTR_Rr2:Other_comparator_specification
bridg:Material.description
urn:CTRPv1.0:FoodProduct.description
bridg:Material.description
urn:CTRPv1.0:Cosmetic.description
bridg:Material.description
urn:CTRPv1.0:Device.description
bridg:Material.description
urn:CTRPv1.0:Biologic.description
bridg:Material.description
urn:CTRPv1.0:Product.description
bridg:Material.description
urn:CTRPv1.0:Drug.description
bridg:Material.description
urn:CTRPv1.0:Material.description
bridg:Material.description
urn:CTRPv1.0:ObservationalStudyProtocol.biospecimenDescription
bridg:Material.description
urn:CTRRr3:Material.description
bridg:Material.description
urn:CTRv1.0:Material.description
in R_Product
bridg:Material.description
urn:ICSRr2:DeviceInstance.desc
in R_Product
bridg:Material.description
urn:ICSRr2:ProductInstance.desc
in R_Product
bridg:Material.description
urn:ICSRr2:Product.desc
in R_Product
bridg:Material.description
urn:ICSRr2:PackagedProduct.desc
in R_Product
bridg:Material.description
urn:ICSRr2:Container.desc
in R_Product
bridg:Material.description
urn:ICSRr2:Substance.desc
bridg:Material.description
urn:caAERSv2.2:Agent.descriptionText
bridg:Material.effectiveDateRange
effectiveDateRange
bridg:Material.effectiveDateRange
false
bridg:Material.effectiveDateRange
The date (and time) span for when the material is active.
bridg:Material.effectiveDateRange
urn:CTOM:Agent.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Biologic.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Product.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Drug.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Product.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Material.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:FoodProduct.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:TherapeuticAgent.StatusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Device.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Cosmetic.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Drug.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Device.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Material.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:TherapeuticProduct.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Biologic.statusCode
bridg:Material.effectiveDateRange
urn:CTRPv1.0:Cosmetic.statusDateRange
bridg:Material.effectiveDateRange
urn:CTRPv1.0:FoodProduct.statusCode
bridg:Material.effectiveDateRange
urn:CTRv1.0:Material.effectiveDateRange
in R_Product
bridg:Material.effectiveDateRange
urn:ICSRr2:ProductInstance.existenceTime
in R_Product
bridg:Material.effectiveDateRange
urn:ICSRr2:DeviceInstance.existenceTime
bridg:Material.formCode
formCode
bridg:Material.formCode
false
bridg:Material.formCode
A coded value specifying the state and nature of the material.
bridg:Material.formCode
solid
bridg:Material.formCode
liquid
bridg:Material.formCode
gas
bridg:Material.formCode
tablet
bridg:Material.formCode
ointment
bridg:Material.formCode
gel
bridg:Material.formCode
urn:AE:Package.formCode
bridg:Material.formCode
urn:AE:Component.formCode
bridg:Material.formCode
urn:AE:Product.formCode
bridg:Material.formCode
urn:CDASHv1.1:EX.EXDOSFRM
bridg:Material.formCode
urn:CDASHv1.1:CM.CMDOSFRM
bridg:Material.formCode
urn:CTOM:AgentOccurrence.formCode
bridg:Material.formCode
urn:CTR_Rr2:Placebo_Pharmaceutical_form
bridg:Material.formCode
urn:CTR_Rr2:IMP_Pharmaceutical_Form
bridg:Material.formCode
urn:CTRPv1.0:Biologic.formCode
bridg:Material.formCode
urn:CTRPv1.0:Cosmetic.formCode
bridg:Material.formCode
urn:CTRPv1.0:Device.formCode
bridg:Material.formCode
urn:CTRPv1.0:Material.formCode
bridg:Material.formCode
urn:CTRPv1.0:Product.formCode
bridg:Material.formCode
urn:CTRPv1.0:FoodProduct.formCode
bridg:Material.formCode
urn:CTRPv1.0:Drug.formCode
bridg:Material.formCode
urn:CTRPv3.8:PlannedSubstanceAdministration.doseFormCode
bridg:Material.formCode
urn:CTRRr3:Material.formCode
bridg:Material.formCode
urn:CTRv1.0:Material.formCode
bridg:Material.formCode
urn:FDA_HL7_SD_SD_DSTU2012:manufacturedMaterial.formCode
bridg:Material.formCode
urn:HL7SD:Product.formCode
in R_Product
bridg:Material.formCode
urn:ICSRr2:Product.formCode
in R_Product
bridg:Material.formCode
urn:ICSRr2:Container.formCode
in R_Product
bridg:Material.formCode
urn:ICSRr2:PackagedProduct.formCode
bridg:Material.formCode
urn:NCI_CRF_Standard:CDE_2179618v1.0:_Agent_Formulation_Descriptive_Text
bridg:Material.formCode
urn:SDTM_IGv3.1.1:CM.CMDOSFRM
bridg:Material.formCode
urn:SDTM_IGv3.1.1:LB.LBSPEC
bridg:Material.formCode
urn:SDTM_IGv3.1.1:EX.EXDOSFRM
bridg:Material.formCode
urn:SDTM_IGv3.1.1:SU.SUDOSFRM
bridg:Material.formCode
urn:SDTM_IGv3.1.2:SU.SUDOSFRM
bridg:Material.formCode
urn:SDTM_IGv3.1.2:EX.EXDOSFRM
bridg:Material.formCode
urn:SDTM_IGv3.1.2:CM.CMDOSFRM
bridg:Material.formCode
urn:caAERSv2.2:CourseAgent.formulation
bridg:MaterialIdentifier.identifier
identifier
bridg:MaterialIdentifier.identifier
false
bridg:MaterialIdentifier.identifier
A unique symbol that establishes identity of the material.
bridg:MaterialIdentifier.identifier
serial number
bridg:MaterialIdentifier.identifier
product number
bridg:MaterialIdentifier.identifier
model number
bridg:MaterialIdentifier.identifier
There are multiple ways in which an identifier can be associated to a product; inherited from MaterialIdentifier.identifier, the association to ProcessedProduct.identifier, and the association to ProductRelationship.identifier. If there is no context associated with the identifier, then MaterialIdentifier.identifier should be used. However, if the identifier for a product would be different in different context, one of the other identifiers should be used. If a kind of product is produced by different processors, and each processor assigns the product a different identifier, then ProcessedProduct.identifier should be used. If the product is used in multiple assemblies, and in each assembly it would be assigned a different identifier, then ProductRelationship.identifier should be used.
bridg:MaterialIdentifier.identifier
urn:AE:Device.modelNumber
bridg:MaterialIdentifier.identifier
urn:AE:Ingredient.batchnumber
bridg:MaterialIdentifier.identifier
urn:AE:Device.serialNumber
bridg:MaterialIdentifier.identifier
urn:AE:Device.otherNumber
bridg:MaterialIdentifier.identifier
urn:AE:Device.catalogNumber
bridg:MaterialIdentifier.identifier
urn:AE:Component.batchNumber
bridg:MaterialIdentifier.identifier
urn:AE:Package.identifier
bridg:MaterialIdentifier.identifier
urn:C3PRv2.9:ScheduledArm.kitNumber
bridg:MaterialIdentifier.identifier
urn:CDASHv1.1:DA.DAREFID
bridg:MaterialIdentifier.identifier
urn:CTOM:Specimen.sampleIdentifier
bridg:MaterialIdentifier.identifier
urn:CTR_Rr2:Related_IMP_sequence_number
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:FoodProduct.identifier
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:Material.identifier
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:Cosmetic.identifier
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:Biologic.identifier
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:Drug.identifier
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:Device.identifier
bridg:MaterialIdentifier.identifier
urn:CTRPv1.0:Product.identifier
bridg:MaterialIdentifier.identifier
urn:CTRRr3:Material.identifier
bridg:MaterialIdentifier.identifier
urn:CTRv1.0:MaterialIdentifier.identifier
bridg:MaterialIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:manufacturedProduct.id
bridg:MaterialIdentifier.identifier
urn:HCTv1.0:CDE_2808120:Anatomic_Structure__System__or_Substance.NMDP_Cord_Blood_Unit_ID:
bridg:MaterialIdentifier.identifier
urn:HCTv1.0:MD_Anderson_Specific_Content:_Transplant.BMT__or_GMP__
CBU ID:
bridg:MaterialIdentifier.identifier
urn:HCTv1.0:CDE_2735595:Anatomic_Structure__System__or_Substance.Non-NMDP_Cord_Blood_Unit
in R_Product
bridg:MaterialIdentifier.identifier
urn:ICSRr2:ProductInstance.id
in R_Specimen universal
bridg:MaterialIdentifier.identifier
urn:ICSRr2:Specimen.id
in R_Product
bridg:MaterialIdentifier.identifier
urn:ICSRr2:IdentifiedItem.id
in R_Product
bridg:MaterialIdentifier.identifier
urn:ICSRr2:DeviceInstance.id
in R_Product
bridg:MaterialIdentifier.identifier
urn:ICSRr2:ManufacturedProduct.id
bridg:MaterialIdentifier.identifier
urn:Lab:Specimen.identifier
bridg:MaterialIdentifier.identifier
urn:LabViewer2.2:Specimen.identifier
bridg:MaterialIdentifier.identifier
urn:SDTM_IGv3.1.2:PC.PCREFID
bridg:MaterialIdentifier.identifier
urn:SDTM_IGv3.1.2:MS.MSREFID
bridg:MaterialIdentifier.identifier
urn:SDTM_IGv3.1.2:MB.MBREFID
bridg:MaterialIdentifier.identifier
urn:SDTM_IGv3.1.2:DA.DAREFID
bridg:MaterialIdentifier.identifier
urn:caAERSv2.2:Agent.nscNumber
bridg:MaterialIdentifier.identifier
urn:caAERSv2.2:MedicalDevice.catalogNumber
bridg:MaterialIdentifier.identifier
urn:caAERSv2.2:MedicalDevice.modelNumber
bridg:MaterialIdentifier.typeCode
typeCode
bridg:MaterialIdentifier.typeCode
false
bridg:MaterialIdentifier.typeCode
A coded value specifying the kind of material identifier.
bridg:MaterialIdentifier.typeCode
urn:CTRv1.0:MaterialIdentifier.typeCode
in R_Product
bridg:MaterialIdentifier.typeCode
urn:ICSRr2:IdentifiedItem.code
bridg:MaterialIdentifier.typeCode
urn:caAERSv2.2:MedicalDevice.modelNumber
bridg:MaterialName.name
name
bridg:MaterialName.name
false
bridg:MaterialName.name
A non-unique textual identifier for the material.
bridg:MaterialName.name
The therapeutic agent used in a chemotherapy clinical trial.
bridg:MaterialName.name
urn:AE:Product.name
bridg:MaterialName.name
urn:AE:Ingredient.name
bridg:MaterialName.name
urn:AE:Component.name
bridg:MaterialName.name
urn:AE:Package.name
bridg:MaterialName.name
urn:CDASHv1.1:SU.SUTRT
bridg:MaterialName.name
urn:CDASHv1.1:CM.CMTRT
bridg:MaterialName.name
urn:CDASHv1.1:EX.EXTRT
bridg:MaterialName.name
urn:CTGOV:Other_Names
bridg:MaterialName.name
urn:CTOM:Agent.name
bridg:MaterialName.name
urn:CTR_Rr2:AS_INN
bridg:MaterialName.name
urn:CTR_Rr2:AS_other_descriptive_name
bridg:MaterialName.name
urn:CTR_Rr2:IMP_Code
bridg:MaterialName.name
urn:CTR_Rr2:IMP_Name
bridg:MaterialName.name
urn:CTR_Rr2:Device_name
bridg:MaterialName.name
urn:CTR_Rr2:IMP_Trade_name
bridg:MaterialName.name
urn:CTRPv1.0:Material.name
bridg:MaterialName.name
urn:CTRPv1.0:Cosmetic.alternateName
bridg:MaterialName.name
urn:CTRPv1.0:Drug.alternateName
bridg:MaterialName.name
urn:CTRPv1.0:FoodProduct.name
bridg:MaterialName.name
urn:CTRPv1.0:Biologic.alternateName
bridg:MaterialName.name
urn:CTRPv1.0:Device.name
bridg:MaterialName.name
urn:CTRPv1.0:Drug.name
bridg:MaterialName.name
urn:CTRPv1.0:FoodProduct.alternateName
bridg:MaterialName.name
urn:CTRPv1.0:Biologic.name
bridg:MaterialName.name
urn:CTRPv1.0:Device.alternateName
bridg:MaterialName.name
urn:CTRPv1.0:Product.name
bridg:MaterialName.name
urn:CTRPv1.0:Cosmetic.name
bridg:MaterialName.name
urn:CTRR:Intervention_Name
s product name(s
bridg:MaterialName.name
urn:CTRR:Comparator
bridg:MaterialName.name
urn:CTRRr3:Material.name
bridg:MaterialName.name
urn:CTRv1.0:MaterialName.name
bridg:MaterialName.name
urn:FDA_HL7_SD_SD_DSTU2012:manufacturedMaterial.name
bridg:MaterialName.name
urn:HCTv1.0:CDE_2960398:Therapies.What_was_the_other_drug_given_for_the_preparative_regimen?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2746348:Techniques.Specify_other_CD3_antibody:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2960392:Therapies.What_was_the_type_of_intrathecal_chemotherapy_given_for_the_preparative_regimen?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2816476:Disease__Disorder_or_Finding.Specify_other_drug_pharmacokinetics_performed_on_to_determine_dosing:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2741515:Therapies.Specify_the_other_type_of_the_monoclonal_antibody_preparative_regimen:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2775844:Therapies.What_was_the_other_hematopoietic__lymphoid_growth_factors__or_cytokines_administered?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2794100:Therapies.Specify_the_other_agent_received_for_infection_prophylaxis:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2741610:Therapies.Specify_the_other_type_of_the_radiolabeled_monoclonal_antibody_preparative_regimen:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2775817:Therapies.What_was_the_specific_G-CSF_drug_administered?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2861458:Therapies.Specify_other_cytokine:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2974115:Therapies.Specify_the_drug_used_to_induce_aplastic_anemia:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2816469:Disease__Disorder_or_Finding.Specify_the_drugs_pharmacokinetics_were_performed_on_to_determine_dosing:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2780779:Therapies.Specify_the_other_additives_that_are_included_in_volume_of_infused_product
bridg:MaterialName.name
urn:HCTv1.0:CDE_2594484:Pharmacologic_Substance.Specify_the_other_agent_used_after_the_start_of_the_preparative_regimen_to_prevent_acute_GVHD_or_graft_rejection
bridg:MaterialName.name
urn:HCTv1.0:CDE_2775819:Therapies.What_was_the_specific_erythropoietin_drug_administered?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2787579:Therapies.Specify_the_other_in_vivo_monoclonal_antibody_administered:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2787667:Therapies.Specify_the_in_vivo_immunotoxin_administered:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2741578:Drug_or_Chemical.What_anticoagulants_were_added_to_the_product_during_collection?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2794436:Therapies.Specify_the_agent_types_received_for_infection_prophylaxis:
bridg:MaterialName.name
urn:HCTv1.0:CDE_3057651:Therapies.Specify_the_other_retinoids_given:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2594466:Pharmacologic_Substance.Specify_the_other_in_vivo_monoclonal_antibody_used_after_the_start_of_the_preparative_regimen_to_prevent_acute_GVHD_or_graft_rejection
bridg:MaterialName.name
urn:HCTv1.0:CDE_2740356:Therapies.What_kind_of_additives_are_included_in_volume_of_infused_product?
bridg:MaterialName.name
urn:HCTv1.0:CDE_3057634:Therapies.Specify_the_other_radioisotope_given:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2787872:Therapies.Specify_the_blinded_randomized_trial_agent_administered:
s of hematopoietic growth factor or cytokine agents given:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2775782:Therapies.Type
bridg:MaterialName.name
urn:HCTv1.0:CDE_2860920:Therapies.Specify_the_other_monoclonal_antibody:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2740983:Therapies.Specify_the_other_type_of_preparative_regimen_medication:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2787876:Therapies.Specify_the_other_agent_administered:
bridg:MaterialName.name
urn:HCTv1.0:CDE_2960478:Therapies.What_type_of_nitrosourea_compound_was_administered?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2958252:Therapies.What_type_of_corticosteroids_were_administered_for_the_preparative_regimen?
bridg:MaterialName.name
urn:HCTv1.0:CDE_2741589:Therapies.Specify_the_other_anticoagulants
bridg:MaterialName.name
urn:HCTv1.0:CDE_2786707:Diagnostic__Therapeutic__and_Research_Equipment.Specify_other_cell_selection_system
bridg:MaterialName.name
urn:HL7SD:Product.name
in R_Product
bridg:MaterialName.name
urn:ICSRr2:Product.name
in R_Product
bridg:MaterialName.name
urn:ICSRr2:DeviceInstance.manufacturerModelName
in R_Product
bridg:MaterialName.name
urn:ICSRr2:MaterialKind.name
in R_Product
bridg:MaterialName.name
urn:ICSRr2:Substance.name
in R_Product
bridg:MaterialName.name
urn:ICSRr2:PackagedProduct.name
in R_Product
bridg:MaterialName.name
urn:ICSRr2:DeviceInstance.softwareName
in R_Product
bridg:MaterialName.name
urn:ICSRr2:NamedEntity.name
bridg:MaterialName.name
urn:NCI_CRF_Standard:CDE_10v4.0:_Agent_Name
bridg:MaterialName.name
urn:NCI_CRF_Standard:CDE_2871652v1.0:_Ingredient_Name
bridg:MaterialName.name
urn:NCI_CRF_Standard:CDE_2179777v2.0:_Concomitant_Agent_Name
bridg:MaterialName.name
urn:SDTM_IGv3.1.1:SU.SUTRT
bridg:MaterialName.name
urn:SDTM_IGv3.1.1:CM.CMTRT
bridg:MaterialName.name
urn:SDTM_IGv3.1.1:EX.EXTRT
bridg:MaterialName.name
urn:SDTM_IGv3.1.1:SU.SUDECOD
bridg:MaterialName.name
urn:SDTM_IGv3.1.1:CM.CMDECOD
bridg:MaterialName.name
urn:SDTM_IGv3.1.2:SU.SUTRT
bridg:MaterialName.name
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_CURTRT
bridg:MaterialName.name
urn:SDTM_IGv3.1.2:CM.CMTRT
bridg:MaterialName.name
urn:SDTM_IGv3.1.2:EX.EXTRT
bridg:MaterialName.name
urn:caAERSv2.2:Agent.name
bridg:MaterialName.name
urn:caAERSv2.2:MedicalDevice.commonName
bridg:MaterialName.name
urn:caAERSv2.2:ConcomitantMedication.agentName
bridg:MaterialName.name
urn:caAERSv2.2:MedicalDevice.brandName
bridg:MaterialName.typeCode
typeCode
bridg:MaterialName.typeCode
false
bridg:MaterialName.typeCode
A coded value specifying the kind of material name.
bridg:MaterialName.typeCode
brand name
bridg:MaterialName.typeCode
urn:CTRv1.0:MaterialName.typeCode
bridg:MaterialName.typeCode
urn:caAERSv2.2:MedicalDevice.brandName
bridg:ObservationResultActionTakenRelationship.delayDuration
delayDuration
bridg:ObservationResultActionTakenRelationship.delayDuration
false
bridg:ObservationResultActionTakenRelationship.delayDuration
The time delay between an observation result being determined and a resulting performed activity action being taken.
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:AE:ProductInvestigation.remedialActionTaken
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:AE:ActionTaken.delayDuration
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:CTOM:AdverseEventTherapy.delayDurationUnitOfMeasureCode
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:CTOM:AdverseEventTherapy.delayDuration
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:CTRv1.0:AdverseEventActionTakenRelationship.delayDuration
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:CTRv1.0:ObservationResultActionTakenRelationship.delayDuration
bridg:ObservationResultActionTakenRelationship.delayDuration
urn:CTRv1.0:ProductActionTakenRelationship.delayDuration
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
samplingMethodCode
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
false
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
A coded value specifying the process used to define a representative set of a population for a study.
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
A Probability Sample: exclusively random process to guarantee that each participant or population has specified chance of selection
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
such as simple random sampling
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
systematic sampling
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
stratified random sampling
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
cluster sampling
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
and consecutive patient sampling.
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
A Non-Probability Sample: any of a variety of other sampling processes
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
such as convenience sampling or invitation to volunteer.
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
urn:CTGOV:Sampling_Method
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
urn:CTRPv1.0:ObservationalStudyProtocol.samplingMethodCode
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
urn:CTRRr3:ObservationalStudy.samplingMethodCode
bridg:ObservationalStudyProtocolVersion.samplingMethodCode
urn:CTRv1.0:ObservationalStudyProtocolVersion.samplingMethodCode
bridg:ObservationalStudyProtocolVersion.specimenAvailableForDNAExtractionIndicator
specimenAvailableForDNAExtractionIndicator
bridg:ObservationalStudyProtocolVersion.specimenAvailableForDNAExtractionIndicator
false
bridg:ObservationalStudyProtocolVersion.specimenAvailableForDNAExtractionIndicator
Specifies whether any biological specimen has the potential for DNA extraction.
bridg:ObservationalStudyProtocolVersion.specimenAvailableForDNAExtractionIndicator
Specimens with the potential for DNA extraction include frozen tissue and whole blood whereas specimens without the potential for DNA extraction include fixed tissue and plasma.
bridg:ObservationalStudyProtocolVersion.specimenAvailableForDNAExtractionIndicator
urn:CTRRr3:StudyAgent.retentionCode
bridg:ObservationalStudyProtocolVersion.specimenRetentionIndicator
specimenRetentionIndicator
bridg:ObservationalStudyProtocolVersion.specimenRetentionIndicator
false
bridg:ObservationalStudyProtocolVersion.specimenRetentionIndicator
Specifies whether a biological specimen is retained beyond the duration of the study.
bridg:ObservationalStudyProtocolVersion.specimenRetentionIndicator
urn:CTRRr3:StudyAgent.retentionCode
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
timePerspectiveCode
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
false
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
A coded value specifying the temporal relationship of observation period to time of subject enrollment.
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
prospective
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
retrospective
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
cross-sectional
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
other
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
urn:CTGOV:Time_Perspective
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
urn:CTRPv1.0:ObservationalStudyProtocol.timePerspectiveCode
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
urn:CTRR:Time_Perspective
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
urn:CTRRr3:ObservationalStudy.timePerspectiveCode
bridg:ObservationalStudyProtocolVersion.timePerspectiveCode
urn:CTRv1.0:ObservationalStudyProtocolVersion.timePerspectiveCode
bridg:Organization.actualIndicator
actualIndicator
bridg:Organization.actualIndicator
false
bridg:Organization.actualIndicator
Specifies whether the organization is a particular instance (actual) vs. universal kind.
bridg:Organization.actualIndicator
To indicate a particular Organization
bridg:Organization.actualIndicator
actualIndicator = "true". To indicate a kind of Organization
bridg:Organization.actualIndicator
actualIndicator = "false".
bridg:Organization.actualIndicator
urn:CTRv1.0:Organization.actualIndicator
Universal
bridg:Organization.actualIndicator
urn:HL7SD:R_AssignedEntity
Universal_COCT_RM_090000UV
bridg:Organization.actualIndicator
urn:HL7SP:R_AssignedEntity
in R_Product
bridg:Organization.actualIndicator
urn:ICSRr2:Organization.determinerCode
in IndividualCaseSafetyReport
bridg:Organization.actualIndicator
urn:ICSRr2:Organization.determinerCode
bridg:Organization.description
description
bridg:Organization.description
false
bridg:Organization.description
The textual representation of the organization.
bridg:Organization.description
urn:C3PR:Organization.descriptionText
bridg:Organization.description
urn:C3PR:InvestigatorGroup.descriptionText
bridg:Organization.description
urn:C3PRv2.9:Organization.descriptionText
bridg:Organization.description
urn:C3PRv2.9:InvestigatorGroup.descriptionText
bridg:Organization.description
urn:CTOM:HealthcareSite.descriptionText
bridg:Organization.description
urn:CTOM:Organization.descriptionText
bridg:Organization.description
urn:CTRPv1.0:Organization.description
bridg:Organization.description
urn:CTRv1.0:Organization.description
bridg:Organization.description
urn:caAERSv2.2:Organization.descriptionText
bridg:Organization.effectiveDateRange
effectiveDateRange
bridg:Organization.effectiveDateRange
false
bridg:Organization.effectiveDateRange
The date (and time) span for when the organization is active.
bridg:Organization.effectiveDateRange
urn:CTRPv3.8:OrganizationalGroup.effectiveDateRange
bridg:Organization.name
name
bridg:Organization.name
false
bridg:Organization.name
A non-unique textual identifier for the organization.
bridg:Organization.name
urn:AE:Authorization.responsibleAuthority
bridg:Organization.name
urn:AE:Reporter.organizationDepartment
bridg:Organization.name
urn:AE:Receiver.organizationDepartment
bridg:Organization.name
urn:AE:Authorization.authorizationHolder
bridg:Organization.name
urn:C3PR:HealthCareSite.name
bridg:Organization.name
urn:C3PR:Organization.name
bridg:Organization.name
urn:C3PR:InvestigatorGroup.name
bridg:Organization.name
urn:C3PR:Study.SponsorCode
bridg:Organization.name
urn:C3PRv2.9:Organization.name
bridg:Organization.name
urn:C3PRv2.9:InvestigatorGroup.name
bridg:Organization.name
urn:CDASHv1.1:LB.LBNAM
bridg:Organization.name
urn:CTGOV:Board_Affiliation
bridg:Organization.name
urn:CTGOV:Responsible_Party_-_Organization
bridg:Organization.name
urn:CTGOV:Oversight_Authorities
bridg:Organization.name
urn:CTGOV:Collaborators
bridg:Organization.name
urn:CTGOV:Board_Name
bridg:Organization.name
urn:CTGOV:Facility_-_Name
bridg:Organization.name
urn:CTGOV:IND/IDE_Grantor
bridg:Organization.name
urn:CTGOV:Sponsor
bridg:Organization.name
urn:CTGOV:Overall_Study_Officials_-_Organizational_Affiliation
bridg:Organization.name
urn:CTOM:Organization.name
bridg:Organization.name
urn:CTOM:HealthcareSite.name
bridg:Organization.name
urn:CTR_Rr2:Source_of_Monetary_or_Material_Support_organisation_name
bridg:Organization.name
urn:CTR_Rr2:Responsible_Site_Organisation
bridg:Organization.name
urn:CTR_Rr2:EV_Sender_ID_organisation
bridg:Organization.name
urn:CTR_Rr2:IEC_Applicant_Organisation
bridg:Organization.name
urn:CTR_Rr2:IEC_Organisation
bridg:Organization.name
urn:CTR_Rr2:CTF_Organisation
bridg:Organization.name
urn:CTR_Rr2:Investigator_Institution_Name
bridg:Organization.name
urn:CTR_Rr2:CA_Applicant_Organisation
bridg:Organization.name
urn:CTR_Rr2:Subcontractor_Department_Name
bridg:Organization.name
urn:CTR_Rr2:CTF_Department
bridg:Organization.name
urn:CTR_Rr2:Network_Organisation
bridg:Organization.name
urn:CTR_Rr2:Sponsor_Organisation
bridg:Organization.name
urn:CTR_Rr2:NCA_Organisation
bridg:Organization.name
urn:CTR_Rr2:Investigator_Institution_Department
bridg:Organization.name
urn:CTR_Rr2:Legal_Rep_Organisation
bridg:Organization.name
urn:CTR_Rr2:Further_information_contact_Organisation
bridg:Organization.name
urn:CTR_Rr2:Subcontractor_Organisation_Name
bridg:Organization.name
urn:CTR_Rr2:MA_Holder
National Competent Authority
bridg:Organization.name
urn:CTR_Rr2:Application_NCA
bridg:Organization.name
urn:CTRPv1.0:Organization.name
bridg:Organization.name
urn:CTRPv1.0:Organization.abbreviatedName
bridg:Organization.name
urn:CTRPv3.8:OrganizationalGroup.name
bridg:Organization.name
urn:CTRPv3.8:StudyIndIde.nihInstholderCode
bridg:Organization.name
urn:CTRPv3.8:HealthCareFacility.name
bridg:Organization.name
urn:CTRPv3.8:StudySite.reviewBoardOrganizationalAffiliation
bridg:Organization.name
urn:CTRPv3.8:Organization.name
bridg:Organization.name
urn:CTRPv3.8:ResearchOrganization.name
bridg:Organization.name
urn:CTRPv3.8:StudyIndIde.nciDivProgHolderCode
bridg:Organization.name
urn:CTRPv3.8:StudyIndIde.grantorCode
bridg:Organization.name
urn:CTRPv3.8:RegulatoryAuthority.name
bridg:Organization.name
urn:CTRR:Secondary_Sponsor
bridg:Organization.name
urn:CTRR:Financial_Sponsor
bridg:Organization.name
urn:CTRR:Oversight_Authority
bridg:Organization.name
urn:CTRR:Trial_Site
bridg:Organization.name
urn:CTRR:Data_Monitoring_Committee
bridg:Organization.name
urn:CTRR:IRB_Affiliation
bridg:Organization.name
urn:CTRR:IRB_Organization
bridg:Organization.name
urn:CTRR:Sponsor
bridg:Organization.name
urn:CTRR:Regulatory_Investigational_Product_Application_Indentifier_Source
bridg:Organization.name
urn:CTRRr3:Organization.name
bridg:Organization.name
urn:CTRRr3:StudyColleague.affiliatedOrganization
bridg:Organization.name
urn:CTRv1.0:Organization.name
bridg:Organization.name
urn:FDA_HL7_SD_SD_DSTU2012:representedOrganization.name
bridg:Organization.name
urn:FDA_HL7_SD_SD_DSTU2012:manufacturerOrganization.name
bridg:Organization.name
urn:HCTv1.0:CDE_2770870:Research_Organizations.Specify_the_name_of_the_institution_that_performed_the_subsequent_HSCT:
bridg:Organization.name
urn:HCTv1.0:CDE_2786700:Techniques.Which_cell_selection_system_was_used_to_manipulated_the_product?
bridg:Organization.name
urn:HCTv1.0:CDE_2682159:DONOR'.Registry_or_UCB_Bank:
bridg:Organization.name
urn:HCTv1.0:CDE_2150//C:Protocol_Administration.Coordinating_Group
bridg:Organization.name
urn:HCTv1.0:CDE_2693479:Recipient_Identification.ID_Assigned_By:_Specify_the_Organization_that_assigned_the_universal_recipeint_ID
bridg:Organization.name
urn:HCTv1.0:CDE_2691464:Techniques.Specify_the_transplant_hospital_unit_name:
bridg:Organization.name
urn:HCTv1.0:CDE_2951981:Lab_Results.Laboratory_Procedure_Source
bridg:Organization.name
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Source_of_Product
bridg:Organization.name
urn:HCTv1.0:CDE_2688299:Techniques.Transplant_Hospital_Name
bridg:Organization.name
urn:HCTv1.0:CDE_2684895:DONOR'.Specify_other_Registry_or_UCB_Bank:
bridg:Organization.name
urn:HCTv1.0:CDE_2771539:Research_Organizations.What_was_the_name_of_the_institution_that_performed_the_DCI:
bridg:Organization.name
urn:HCTv1.0:CDE_2693488:Property_or_Attribute.Specify_the_organization_that_assigned_the_universal_recipient_ID:
bridg:Organization.name
urn:HCTv1.0:CDE_2688301:Techniques.Transplant_Hospital_Unit_Name
bridg:Organization.name
urn:HCTv1.0:CDE_3158520:Protocol_Administration.Specify_the_other_group_that_is_administering_the_clinical_trial:
HSCT : Part 1 of 4.If the institution where previous HSCT was performed is different from the current HSCT, what is the name of the institution?
bridg:Organization.name
urn:HCTv1.0:CDE_2532036:Hematopoietic_Stem_Cell_Transplant
bridg:Organization.name
urn:HL7SP:Organization.name
bridg:Organization.name
urn:HL7SP:EthicalCommittee.name
bridg:Organization.name
urn:HSDBv1.0:[IND/IDE]_.NIH_Institution
bridg:Organization.name
urn:HSDBv1.0:[Sponsor].Organization_Name
bridg:Organization.name
urn:HSDBv1.0:[Summary_4_Funder].Organization_Name
bridg:Organization.name
urn:HSDBv1.0:[IRB].IRB_of_record
bridg:Organization.name
urn:HSDBv1.0:[Lead_Organization].Name
bridg:Organization.name
urn:HSDBv1.0:[IND/IDE]_.Holder_Type
bridg:Organization.name
urn:HSDBv1.0:[Study].Responsible_Party
in IndividualCaseSafetyReport
bridg:Organization.name
urn:ICSRr2:Organization.name
in R_Product
bridg:Organization.name
urn:ICSRr2:ProductIdentifierIssuer.name
in R_Product
bridg:Organization.name
urn:ICSRr2:Agency.name
in R_Product
bridg:Organization.name
urn:ICSRr2:Organization.name
bridg:Organization.name
urn:Lab:Organization.name
bridg:Organization.name
urn:Lab:PerformingLaboratory.name
bridg:Organization.name
urn:Lab:CentralLaboratory.name
bridg:Organization.name
urn:Lab:HealthCareSite.name
bridg:Organization.name
urn:LabViewer2.2:CentralLaboratory.name
bridg:Organization.name
urn:LabViewer2.2:Identifier.assigningAuthorityName
bridg:Organization.name
urn:LabViewer2.2:Organization.name
bridg:Organization.name
urn:LabViewer2.2:HealthcareSite.name
bridg:Organization.name
urn:LabViewer2.2:PerformingLaboratory.name
bridg:Organization.name
urn:NCI_CRF_Standard:CDE_2841282v1.0:_Performing_Laboratory_Name_Text
bridg:Organization.name
urn:NCI_CRF_Standard:CDE_2551737v1.0:_Registration_Name_Institution_Institution_Name
bridg:Organization.name
urn:PSC:Site.name
bridg:Organization.name
urn:PSCv2.6:Site.name
bridg:Organization.name
urn:SDTM_IGv3.1.1:EG.EGNAM
bridg:Organization.name
urn:SDTM_IGv3.1.1:LB.LBNAM
bridg:Organization.name
urn:SDTM_IGv3.1.2:LB.LBNAM
bridg:Organization.name
urn:SDTM_IGv3.1.2:MS.MSNAM
bridg:Organization.name
urn:SDTM_IGv3.1.2:MB.MBNAM
bridg:Organization.name
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_SPONSOR
bridg:Organization.name
urn:SDTM_IGv3.1.2:PC.PCNAM
bridg:Organization.name
urn:SDTM_IGv3.1.2:EG.EGNAM
bridg:Organization.name
urn:WHO:Primary_Sponsor
bridg:Organization.name
urn:WHO:Contact_for_Public_Queries_-_affiliation
s
bridg:Organization.name
urn:WHO:Secondary_Sponsor
s of Monetary or Material Support
bridg:Organization.name
urn:WHO:Source
bridg:Organization.name
urn:caAERSv2.2:Organization.name
bridg:Organization.name
urn:caAERSv2.2:MedicalDevice.manufacturerName
bridg:Organization.name
urn:caAERSv2.2:MedicalDevice.reprocessorName
bridg:Organization.name
urn:caAERSv2.2:Recipient.name
bridg:Organization.postalAddress
postalAddress
bridg:Organization.postalAddress
false
bridg:Organization.postalAddress
A contact point used to send physical forms of communication to the organization.
bridg:Organization.postalAddress
urn:C3PR:Address.countryCode
bridg:Organization.postalAddress
urn:C3PR:Address.postalCode
bridg:Organization.postalAddress
urn:C3PR:Address.streetAddress
bridg:Organization.postalAddress
urn:C3PR:Address.stateCode
bridg:Organization.postalAddress
urn:C3PR:Address.cityCode
bridg:Organization.postalAddress
urn:C3PRv2.9:Address
bridg:Organization.postalAddress
urn:CTGOV:Facility_-_State/Province
bridg:Organization.postalAddress
urn:CTGOV:Facility_-_Country
bridg:Organization.postalAddress
urn:CTGOV:Facility_-_Postal_Code
bridg:Organization.postalAddress
urn:CTGOV:Facility_-_City
bridg:Organization.postalAddress
urn:CTOM:Organization.city
bridg:Organization.postalAddress
urn:CTOM:Organization.postalCode
bridg:Organization.postalAddress
urn:CTOM:Organization.stateCode
bridg:Organization.postalAddress
urn:CTOM:Organization.countryCode
bridg:Organization.postalAddress
urn:CTR_Rr2:IEC_Street_Address
member state
bridg:Organization.postalAddress
urn:CTR_Rr2:Application_MS
bridg:Organization.postalAddress
urn:CTR_Rr2:NCA_Street_Address
bridg:Organization.postalAddress
urn:CTR_Rr2:NCA_Country
bridg:Organization.postalAddress
urn:CTR_Rr2:Responsible_Site_Country
bridg:Organization.postalAddress
urn:CTR_Rr2:Source_of_Monetary_or_Material_Support_country
bridg:Organization.postalAddress
urn:CTR_Rr2:Responsible_Site_Post_Code
bridg:Organization.postalAddress
urn:CTR_Rr2:IEC_Post_Code
bridg:Organization.postalAddress
urn:CTR_Rr2:Responsible_Site_Street_Address
bridg:Organization.postalAddress
urn:CTR_Rr2:IEC_Country
bridg:Organization.postalAddress
urn:CTR_Rr2:IEC_Town/City
bridg:Organization.postalAddress
urn:CTR_Rr2:NCA_Post_Code
bridg:Organization.postalAddress
urn:CTR_Rr2:Responsible_Site_Town/City
bridg:Organization.postalAddress
urn:CTR_Rr2:NCA_Town/City
bridg:Organization.postalAddress
urn:CTRPv1.0:Organization.postalAddress
bridg:Organization.postalAddress
urn:CTRPv3.8:ResearchOrganization.postalAddress
bridg:Organization.postalAddress
urn:CTRPv3.8:Organization.postalAddress
bridg:Organization.postalAddress
urn:CTRRr3:Organization.postalAddress
bridg:Organization.postalAddress
urn:CTRv1.0:Organization.postalAddress
bridg:Organization.postalAddress
urn:FDA_HL7_SD_SD_DSTU2012:representedOrganization.addr
bridg:Organization.postalAddress
urn:FDA_HL7_SD_SD_DSTU2012:manufacturerOrganization.addr
HSCT : Part 1 of 4.If the institution where previous HSCT was performed is different from the current HSCT, what is the state where the institution is located?
bridg:Organization.postalAddress
urn:HCTv1.0:CDE_2686045:Hematopoietic_Stem_Cell_Transplant
HSCT : Part 1 of 4.If the institution where previous HSCT was performed is different from the current HSCT, what is the country where the institution is located?
bridg:Organization.postalAddress
urn:HCTv1.0:CDE_2684981:Hematopoietic_Stem_Cell_Transplant
HSCT : Part 1 of 4.If the institution where previous HSCT was performed is different from the current HSCT, what is the city where the institution is located?
bridg:Organization.postalAddress
urn:HCTv1.0:CDE_2532039:Hematopoietic_Stem_Cell_Transplant
bridg:Organization.postalAddress
urn:HL7SP:Organization.addr
bridg:Organization.postalAddress
urn:HL7SP:EthicalCommittee.addr
bridg:Organization.postalAddress
urn:HSDBv1.0:[Summary_4_Funder].Country
bridg:Organization.postalAddress
urn:HSDBv1.0:[Summary_4_Funder].Street_Address
bridg:Organization.postalAddress
urn:HSDBv1.0:[Lead_Organization]._Zip/Postal_code
bridg:Organization.postalAddress
urn:HSDBv1.0:[Sponsor].City
bridg:Organization.postalAddress
urn:HSDBv1.0:[Lead_Organization].Country
bridg:Organization.postalAddress
urn:HSDBv1.0:[Sponsor].Country
bridg:Organization.postalAddress
urn:HSDBv1.0:[Summary_4_Funder].Zip/Postal_code
bridg:Organization.postalAddress
urn:HSDBv1.0:[Sponsor].State/Province
bridg:Organization.postalAddress
urn:HSDBv1.0:[Sponsor].Street_Address
bridg:Organization.postalAddress
urn:HSDBv1.0:[Sponsor].Zip/Postal_code
bridg:Organization.postalAddress
urn:HSDBv1.0:[Summary_4_Funder].State/Province
bridg:Organization.postalAddress
urn:HSDBv1.0:[Lead_Organization]._State/Province
bridg:Organization.postalAddress
urn:HSDBv1.0:[Lead_Organization].Street_Address
bridg:Organization.postalAddress
urn:HSDBv1.0:[Summary_4_Funder].City
bridg:Organization.postalAddress
urn:HSDBv1.0:[Lead_Organization]._City
in IndividualCaseSafetyReport
bridg:Organization.postalAddress
urn:ICSRr2:Organization.addr
in R_Product
bridg:Organization.postalAddress
urn:ICSRr2:Organization.addr
bridg:Organization.postalAddress
urn:SDTM_IGv3.1.1:DM.COUNTRY
bridg:Organization.postalAddress
urn:SDTM_IGv3.1.2:DM.COUNTRY
bridg:Organization.postalAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:Organization.telecomAddress
telecomAddress
bridg:Organization.telecomAddress
false
bridg:Organization.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the organization.
bridg:Organization.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:Organization.telecomAddress
urn:C3PRv2.9:ContactMechanismBasedRecipient
bridg:Organization.telecomAddress
urn:C3PRv2.9:ContactMechanism.value
bridg:Organization.telecomAddress
urn:C3PRv2.9:ContactMechanism.type
bridg:Organization.telecomAddress
urn:CTOM:HealthcareSite.telecomAddress
bridg:Organization.telecomAddress
urn:CTOM:Organization.telecomAddress
bridg:Organization.telecomAddress
urn:CTRPv1.0:Organization.telecomAddress
bridg:Organization.telecomAddress
urn:CTRPv3.8:ResearchOrganization.telecomAddress
bridg:Organization.telecomAddress
urn:CTRPv3.8:Organization.telecomAddress
bridg:Organization.telecomAddress
urn:CTRRr3:Organization.telecomAddress
bridg:Organization.telecomAddress
urn:CTRv1.0:Organization.telecomAddress
bridg:Organization.telecomAddress
urn:FDA_HL7_SD_SD_DSTU2012:representedOrganization.telecom
bridg:Organization.telecomAddress
urn:FDA_HL7_SD_SD_DSTU2012:manufacturerOrganization.telecom
bridg:Organization.telecomAddress
urn:HL7SP:EthicalCommittee.telecom
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Summary_4_Funder].TTY
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Sponsor].FAX
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Lead_Organization].TTY
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Lead_Organization].Email_Address
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Sponsor].URL
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Summary_4_Funder].URL
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Lead_Organization].URL
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Summary_4_Funder].FAX
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Lead_Organization].FAX
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Sponsor].Email_Address
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Summary_4_Funder].Email_Address
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Lead_Organization].Phone
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Sponsor].Phone
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Sponsor].TTY
bridg:Organization.telecomAddress
urn:HSDBv1.0:[Summary_4_Funder].Phone
in IndividualCaseSafetyReport
bridg:Organization.telecomAddress
urn:ICSRr2:Organization.telecom
in R_Product
bridg:Organization.telecomAddress
urn:ICSRr2:Organization.telecom
bridg:Organization.telecomAddress
urn:Lab:HealthcareSite.telecomAddress
bridg:Organization.telecomAddress
urn:caAERSv2.2:ScheduledEmailNotification.to
bridg:Organization.telecomAddress
urn:caAERSv2.2:ReportVersion.email
bridg:Organization.telecomAddress
urn:caAERSv2.2:ReportDelivery.address
bridg:Organization.telecomAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:Organization.typeCode
typeCode
bridg:Organization.typeCode
false
bridg:Organization.typeCode
A coded value specifying the kind of organization.
bridg:Organization.typeCode
academic
bridg:Organization.typeCode
pharmaceutical industry
bridg:Organization.typeCode
government
bridg:Organization.typeCode
other
bridg:Organization.typeCode
commercial
bridg:Organization.typeCode
non-commercial [example from EudraCT]
bridg:Organization.typeCode
urn:CTR_Rr2:Sponsor_Status
bridg:Organization.typeCode
urn:CTRPv3.8:StudyIndIde.holderTypeCode
bridg:Organization.typeCode
urn:CTRR:Sponsor_Organization_Type
bridg:Organization.typeCode
urn:CTRv1.0:Organization.typeCode
bridg:Organization.typeCode
urn:FDA_HL7_SD_SD_DSTU2012:serviceDeliveryLocation/serviceProviderOrganizationKind.code
bridg:Organization.typeCode
urn:HSDBv1.0:[IND/IDE]_.Holder_Type
bridg:Organization.typeCode
urn:PRM:Sponsor_Organization_Type
bridg:OrganizationIdentifier.identifier
identifier
bridg:OrganizationIdentifier.identifier
false
bridg:OrganizationIdentifier.identifier
A unique symbol that establishes identity of the organization.
bridg:OrganizationIdentifier.identifier
In cases of laboratories this is the Clinical Laboratory Improvement Act/Amendment (CLIA) ID.
bridg:OrganizationIdentifier.identifier
urn:C3PR:Organization.nciInstituteCode
bridg:OrganizationIdentifier.identifier
urn:C3PR:OrganizationAssignedIdentifier
bridg:OrganizationIdentifier.identifier
urn:C3PRv2.9:Identifier.value
bridg:OrganizationIdentifier.identifier
urn:CTOM:Protocol.monitorCode
bridg:OrganizationIdentifier.identifier
urn:CTR_Rr2:EV_Sender_ID
bridg:OrganizationIdentifier.identifier
urn:CTRPv1.0:Organization.identifier
bridg:OrganizationIdentifier.identifier
urn:CTRPv3.8:StudyResourcing.organizationIdentifier
bridg:OrganizationIdentifier.identifier
urn:CTRPv3.8:Organization.identifier
bridg:OrganizationIdentifier.identifier
urn:CTRPv3.8:IdentifiedEntity.assignedIdentifier
bridg:OrganizationIdentifier.identifier
urn:CTRRr3:Organization.identifier
bridg:OrganizationIdentifier.identifier
urn:CTRv1.0:OrganizationIdentifier.identifier
bridg:OrganizationIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:representedOrganization.id
bridg:OrganizationIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:manufacturerOrganization.id
bridg:OrganizationIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol//plannedStudy/location/serviceDeliveryLocation.id
bridg:OrganizationIdentifier.identifier
urn:HCTv1.0:CDE_3115632:Medical_Records_and_Forms.Clinic_and_Hospital_ID:
bridg:OrganizationIdentifier.identifier
urn:HCTv1.0:CDE_3115737:Medical_Records_and_Forms.If_necessary__please_validate_the_patient_and_clinic_and_hospital_ID_response.
bridg:OrganizationIdentifier.identifier
urn:HCTv1.0:CDE_3126035:Medical_Records_and_Forms.European_Group_for_Blood_And_Marrow_Transplantation_Center_Number:
bridg:OrganizationIdentifier.identifier
urn:HCTv1.0:CDE_2527895:Individuals.Hematopoietic_Stem_Cell_Transplantation_Recipient_CIBMTR_Center_Number:
CIC Number
bridg:OrganizationIdentifier.identifier
urn:HCTv1.0:CDE_2688251:Data_Source.EBMT_Code
bridg:OrganizationIdentifier.identifier
urn:HL7SP:EthicalCommittee.id
bridg:OrganizationIdentifier.identifier
urn:HL7SP:Organization.id
bridg:OrganizationIdentifier.identifier
urn:HSDBv1.0:[Sponsor].Federal_employer_ID_no
bridg:OrganizationIdentifier.identifier
urn:HSDBv1.0:[Sponsor].IORG_number
bridg:OrganizationIdentifier.identifier
urn:HSDBv1.0:[Summary_4_Funder].IORG_number
bridg:OrganizationIdentifier.identifier
urn:HSDBv1.0:[Lead_Organization].IORG_number
in R_Product
bridg:OrganizationIdentifier.identifier
urn:ICSRr2:ProductIdentifierIssuer.id
in IndividualCaseSafetyReport
bridg:OrganizationIdentifier.identifier
urn:ICSRr2:IdentifiedEntity2.id
in R_Product
bridg:OrganizationIdentifier.identifier
urn:ICSRr2:Organization.id
in R_Product
bridg:OrganizationIdentifier.identifier
urn:ICSRr2:Agency.id
in IndividualCaseSafetyReport
bridg:OrganizationIdentifier.identifier
urn:ICSRr2:TerritorialAuthority.id
bridg:OrganizationIdentifier.identifier
urn:Lab:Organization.identifier
bridg:OrganizationIdentifier.identifier
urn:LabViewer2.2:Organization.identifier
bridg:OrganizationIdentifier.identifier
urn:LabViewer2.2:HealthcareSite.identifier
bridg:OrganizationIdentifier.identifier
urn:caAERSv2.2:Organization.nciInstituteCode
bridg:OrganizationIdentifier.primaryIndicator
primaryIndicator
bridg:OrganizationIdentifier.primaryIndicator
false
bridg:OrganizationIdentifier.primaryIndicator
Specifies whether this is the main or principal organization identifier.
bridg:OrganizationIdentifier.primaryIndicator
urn:C3PRv2.9:Identifier.primaryIndicator
bridg:OrganizationIdentifier.primaryIndicator
urn:CTRv1.0:OrganizationIdentifier.primaryIndicator
bridg:OrganizationIdentifier.typeCode
typeCode
bridg:OrganizationIdentifier.typeCode
false
bridg:OrganizationIdentifier.typeCode
A coded value specifying the kind of organization identifier.
bridg:OrganizationIdentifier.typeCode
urn:C3PR:Identifier.type
bridg:OrganizationIdentifier.typeCode
urn:C3PRv2.9:Identifier.typeInternal
bridg:OrganizationIdentifier.typeCode
urn:C3PRv2.9:OrganizationAssignedIdentifier
bridg:OrganizationIdentifier.typeCode
urn:CTRPv1.0:IdentifiedBiologicEntity.typeCode
bridg:OrganizationIdentifier.typeCode
urn:CTRv1.0:OrganizationIdentifier.typeCode
in IndividualCaseSafetyReport
bridg:OrganizationIdentifier.typeCode
urn:ICSRr2:IdentifiedEntity2.code
bridg:OrganizationRelationship.effectiveDateRange
effectiveDateRange
bridg:OrganizationRelationship.effectiveDateRange
false
bridg:OrganizationRelationship.effectiveDateRange
The date (and time) span for when the organization relationship is active.
bridg:OrganizationRelationship.effectiveDateRange
urn:CTRPv3.8:OrganizationalRelationship.effectiveDateRange
bridg:OrganizationRelationship.effectiveDateRange
urn:CTRPv3.8:OrganizationalGroupRelationship.effectiveDateRange
bridg:OrganizationRelationship.effectiveDateRange
urn:CTRv1.0:OrganizationRelationship.effectiveDateRange
Universal_COCT_RM_150000UV
bridg:OrganizationRelationship.effectiveDateRange
urn:HL7SP:E_Organization
bridg:OrganizationRelationship.typeCode
typeCode
bridg:OrganizationRelationship.typeCode
false
bridg:OrganizationRelationship.typeCode
A coded value specifying the kind of organization relationship.
bridg:OrganizationRelationship.typeCode
part
bridg:OrganizationRelationship.typeCode
department
bridg:OrganizationRelationship.typeCode
center
bridg:OrganizationRelationship.typeCode
legal representative
bridg:OrganizationRelationship.typeCode
This is HL7 structured vocabulary and is part of a controlled vocabulary set.
Independent Ethics Committee Applicant Type
bridg:OrganizationRelationship.typeCode
urn:CTR_Rr2:IEC
bridg:OrganizationRelationship.typeCode
urn:CTRPv3.8:OrganizationalRelationship.typeCode
bridg:OrganizationRelationship.typeCode
urn:CTRPv3.8:OrganizationalGroupRelationship.typeCode
bridg:OrganizationRelationship.typeCode
urn:CTRRr3:OrganizationRelationship.typeCode
bridg:OrganizationRelationship.typeCode
urn:CTRv1.0:OrganizationRelationship.typeCode
Universal_COCT_RM_150000UV
bridg:OrganizationRelationship.typeCode
urn:HL7SP:E_Organization
in R_Product
bridg:OrganizationRelationship.typeCode
urn:ICSRr2:AssignedEntity.code
in R_Product
bridg:OrganizationRelationship.typeCode
urn:ICSRr2:AssignedEntity3.code
bridg:OrganizationalContact.effectiveDateRange
effectiveDateRange
bridg:OrganizationalContact.effectiveDateRange
false
bridg:OrganizationalContact.effectiveDateRange
The date (and time) span for when the organizational contact is active.
bridg:OrganizationalContact.effectiveDateRange
urn:CTRPv1.0:OrganizationalContact.statusDateRange
bridg:OrganizationalContact.effectiveDateRange
urn:CTRPv3.8:StructuralRole.statusCode
bridg:OrganizationalContact.effectiveDateRange
urn:CTRv1.0:OrganizationalContact.effectiveDateRange
bridg:OrganizationalContact.postalAddress
postalAddress
bridg:OrganizationalContact.postalAddress
false
bridg:OrganizationalContact.postalAddress
A contact point used to send physical forms of communication to the organizational contact.
bridg:OrganizationalContact.postalAddress
urn:AE:ContactPerson.address
bridg:OrganizationalContact.postalAddress
urn:CTGOV:Board_Contact_mailing_address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Network_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CTF_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CA_Applicant_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Subcontractor_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:IEC_Applicant_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CTF_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:IEC_Applicant_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Network_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CA_Applicant_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Sponsor_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Legal_Rep_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Sponsor_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Subcontractor_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CTF_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Legal_Rep_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CA_Applicant_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CA_Applicant_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Network_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Sponsor_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Sponsor_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:IEC_Applicant_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:IEC_Applicant_Street_Address
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Network_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Legal_Rep_Country
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Subcontractor_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Legal_Rep_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:Subcontractor_Post_Code
bridg:OrganizationalContact.postalAddress
urn:CTR_Rr2:CTF_Street_Town/City
bridg:OrganizationalContact.postalAddress
urn:CTRPv1.0:OrganizationalContact.postalAddress
bridg:OrganizationalContact.postalAddress
urn:CTRPv3.8:PersonRole.postalAddress
bridg:OrganizationalContact.postalAddress
urn:CTRRr3:OrganizationalContact.postalAddress
bridg:OrganizationalContact.postalAddress
urn:CTRv1.0:OrganizationalContact.postalAddress
bridg:OrganizationalContact.postalAddress
urn:FDA_HL7_SD_SD_DSTU2012:contactParty.addr
bridg:OrganizationalContact.postalAddress
urn:FDA_HL7_SD_SD_DSTU2012:manufacturerOrganization/contactParty.addr
bridg:OrganizationalContact.postalAddress
urn:HSDBv1.0:[Sponsor_Contact].City
bridg:OrganizationalContact.postalAddress
urn:HSDBv1.0:[Sponsor_Contact].Zip/Postal_code
bridg:OrganizationalContact.postalAddress
urn:HSDBv1.0:[Sponsor_Contact].Street_Address
bridg:OrganizationalContact.postalAddress
urn:HSDBv1.0:[Sponsor_Contact].Country
bridg:OrganizationalContact.postalAddress
urn:HSDBv1.0:[Sponsor_Contact].State/Province
in E_Organization informational
bridg:OrganizationalContact.postalAddress
urn:ICSRr2:ContactParty.addr
in IndividualCaseSafetyReport
bridg:OrganizationalContact.postalAddress
urn:ICSRr2:ContactParty.addr
in R_Product
bridg:OrganizationalContact.postalAddress
urn:ICSRr2:contactParty.addr
bridg:OrganizationalContact.primaryIndicator
primaryIndicator
bridg:OrganizationalContact.primaryIndicator
false
bridg:OrganizationalContact.primaryIndicator
Specifies whether this is the main or principal organizational contact.
bridg:OrganizationalContact.primaryIndicator
urn:CTRPv1.0:OrganizationalContact.primaryIndicator
bridg:OrganizationalContact.primaryIndicator
urn:CTRv1.0:OrganizationalContact.primaryIndicator
bridg:OrganizationalContact.telecomAddress
telecomAddress
bridg:OrganizationalContact.telecomAddress
false
bridg:OrganizationalContact.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the organizational contact.
bridg:OrganizationalContact.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:OrganizationalContact.telecomAddress
urn:AE:ContactPerson.phoneNumber
bridg:OrganizationalContact.telecomAddress
urn:C3PR:ContactMechanism.value
bridg:OrganizationalContact.telecomAddress
urn:C3PR:ContactMechanism.type
bridg:OrganizationalContact.telecomAddress
urn:CTGOV:Board_Contact_Email
bridg:OrganizationalContact.telecomAddress
urn:CTGOV:Board_Contact_Ext
bridg:OrganizationalContact.telecomAddress
urn:CTGOV:Board_Contact_Phone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:IEC_Applicant_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:CA_Applicant_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:CTF_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:IEC_Applicant_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Network_Email
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Sponsor_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:IEC_Applicant_Email
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Subcontractor_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Subcontractor_Email
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Subcontractor_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Network_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:CTF_Email
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Sponsor_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Legal_Rep_Telephone
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:CTF_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:CA_Applicant_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Legal_Rep_Email
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Network_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Sponsor_Email
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:Legal_Rep_Fax
bridg:OrganizationalContact.telecomAddress
urn:CTR_Rr2:CA_Applicant_Email
bridg:OrganizationalContact.telecomAddress
urn:CTRPv3.8:PersonRole.telecomAddress
bridg:OrganizationalContact.telecomAddress
urn:CTRRr3:OrganizationalContact.telecomAddress
bridg:OrganizationalContact.telecomAddress
urn:CTRv1.0:OrganizationalContact.telecomAddress
bridg:OrganizationalContact.telecomAddress
urn:FDA_HL7_SD_SD_DSTU2012:contactParty.telecom
bridg:OrganizationalContact.telecomAddress
urn:FDA_HL7_SD_SD_DSTU2012:manufacturerOrganization/contactParty.telecom
bridg:OrganizationalContact.telecomAddress
urn:HSDBv1.0:[Sponsor_Contact].URL
bridg:OrganizationalContact.telecomAddress
urn:HSDBv1.0:[Sponsor_Contact].FAX
bridg:OrganizationalContact.telecomAddress
urn:HSDBv1.0:[Sponsor_Contact].TTY
bridg:OrganizationalContact.telecomAddress
urn:HSDBv1.0:[Sponsor_Contact].Phone
bridg:OrganizationalContact.telecomAddress
urn:HSDBv1.0:[Sponsor_Contact].Email_Address
in IndividualCaseSafetyReport
bridg:OrganizationalContact.telecomAddress
urn:ICSRr2:ContactParty.telecom
in R_Product
bridg:OrganizationalContact.telecomAddress
urn:ICSRr2:contactParty.telecom
in E_Organization informational
bridg:OrganizationalContact.telecomAddress
urn:ICSRr2:ContactParty.telecom
bridg:OrganizationalContact.title
title
bridg:OrganizationalContact.title
false
bridg:OrganizationalContact.title
A descriptive or distinctive appellation, especially one belonging to a person by right of rank, office, attainment, etc.
bridg:OrganizationalContact.title
urn:CTRPv1.0:OraganizationalContact.title
bridg:OrganizationalContact.title
urn:CTRPv3.8:OrganizationalContact.title
bridg:OrganizationalContact.title
urn:CTRv1.0:OrganizationalContact.title
bridg:OrganizationalContact.typeCode
typeCode
bridg:OrganizationalContact.typeCode
false
bridg:OrganizationalContact.typeCode
A coded value specifying the kind of organizational contact.
bridg:OrganizationalContact.typeCode
safety
bridg:OrganizationalContact.typeCode
sales
bridg:OrganizationalContact.typeCode
financial
bridg:OrganizationalContact.typeCode
manufacturing
bridg:OrganizationalContact.typeCode
Review Board contact
bridg:OrganizationalContact.typeCode
urn:CTGOV:Board_Contact
bridg:OrganizationalContact.typeCode
urn:CTRPv1.0:OrganizationalContact.typeCode
bridg:OrganizationalContact.typeCode
urn:CTRPv3.8:OrganizationalContact.typeCode
bridg:OrganizationalContact.typeCode
urn:CTRRr3:OrganizationalContact.typeCode
bridg:OrganizationalContact.typeCode
urn:CTRv1.0:OrganizationalContact.typeCode
bridg:OversightCommittee.effectiveDateRange
effectiveDateRange
bridg:OversightCommittee.effectiveDateRange
false
bridg:OversightCommittee.effectiveDateRange
The date (and time) span for when the oversight committee is active.
bridg:OversightCommittee.effectiveDateRange
urn:CTRPv1.0:OversightCommittee.statusDateRange
bridg:OversightCommittee.effectiveDateRange
urn:CTRPv1.0:OversightCommittee.statusCode
bridg:OversightCommittee.effectiveDateRange
urn:CTRv1.0:OversightCommittee.effectiveDateRange
bridg:OversightCommittee.typeCode
typeCode
bridg:OversightCommittee.typeCode
false
bridg:OversightCommittee.typeCode
A coded value specifying the kind of oversight committee.
bridg:OversightCommittee.typeCode
Adjudication Committee
bridg:OversightCommittee.typeCode
IRB
bridg:OversightCommittee.typeCode
Data Safety Monitoring Board
bridg:OversightCommittee.typeCode
urn:CTOM:Data_Monitoring_Committee
bridg:OversightCommittee.typeCode
urn:CTRPv1.0:OversightCommittee.typeCode
bridg:OversightCommittee.typeCode
urn:CTRPv3.8:OversightCommittee.typeCode
bridg:OversightCommittee.typeCode
urn:CTRR:IRB_Affiliation
bridg:OversightCommittee.typeCode
urn:CTRR:Oversight_Authority
bridg:OversightCommittee.typeCode
urn:CTRR:IRB_Organization
bridg:OversightCommittee.typeCode
urn:CTRRr3:OversightCommittee.typeCode
bridg:OversightCommittee.typeCode
urn:CTRv1.0:OversightCommittee.typeCode
bridg:OversightCommittee.typeCode
urn:HSDBv1.0:[IRB].IRB_type
bridg:Package.capTypeCode
capTypeCode
bridg:Package.capTypeCode
false
bridg:Package.capTypeCode
A coded value specifying the type of container cap.
bridg:Package.capTypeCode
film
bridg:Package.capTypeCode
foil
bridg:Package.capTypeCode
In some cases, it is important for this to be consistent with decapping, piercing or other automated manipulation.
bridg:Package.capTypeCode
urn:AE:Package.capTypeCode
bridg:Package.capTypeCode
urn:CTRv1.0:Package.capTypeCode
in R_Product
bridg:Package.capTypeCode
urn:ICSRr2:PackagedProduct.capTypeCode
bridg:Package.capacityQuantity
capacityQuantity
bridg:Package.capacityQuantity
false
bridg:Package.capacityQuantity
The maximum number of product units within a package.
bridg:Package.capacityQuantity
1000 cc.
bridg:Package.capacityQuantity
urn:AE:Package.capacityQuantity
bridg:Package.capacityQuantity
urn:CTRv1.0:Package.capacityQuantity
in R_Product
bridg:Package.capacityQuantity
urn:ICSRr2:PackagedProduct.capacityQuantity
bridg:Package.handlingCode
handlingCode
bridg:Package.handlingCode
false
bridg:Package.handlingCode
A coded value specifying special handling requirements for the package.
bridg:Package.handlingCode
keep at room temperature
bridg:Package.handlingCode
store upright
bridg:Package.handlingCode
urn:CTRv1.0:Package.handlingCode
in R_Product
bridg:Package.handlingCode
urn:ICSRr2:Product.handlingCode
bridg:PerformedActivity.dateRange
dateRange
bridg:PerformedActivity.dateRange
false
bridg:PerformedActivity.dateRange
The date and time span when this activity began and ended.
bridg:PerformedActivity.dateRange
The date and time when a sample is taken from the subject.
bridg:PerformedActivity.dateRange
A dose of chemotherapy is given on June 12th starting at 9am and finishing at 12pm.
bridg:PerformedActivity.dateRange
Whether administrative or preparatory activities are included in this time frame is up to whoever is defining the activity - this time frame is all that matters when the activity occurred.
The date range is an interval (IVL) data type, meaning it has a beginning (low) and end (high) values. It is also a datetime (TS.DATETIME) data type, meaning the beginning date and the end date can have uncertain values (e.g., a range). For example, if a subject was diagnosed with leukemia sometime in 2009 and that subject had a transplant (substance administration) sometime in 2010. We can surmise that the subject must have had a preparative regimen sometime between those times. Therefore the preparative regimen activity would have a beginning (low) date range of between 2009-01-01 and 2009-12-31; and an ending (high) date range of between 2010-01-01 and 2010-12-31. The precise data type mappings would be:
IVL<TS.DATETIME>.low.uncertainRange.low = 2009-01-01
IVL<TS.DATETIME>.low.uncertainRange.high = 2009-12-31
IVL<TS.DATETIME>.high.uncertainRange.low = 2010-01-01
IVL<TS.DATETIME>.high.uncertainRange.high = 2010-12-31
[Note that times are left out of the example to keep it as simple as possible.]
bridg:PerformedActivity.dateRange
urn:AE:ProductInvestigation.investigationDate
bridg:PerformedActivity.dateRange
urn:AE:AdverseEvent.baselineDate
bridg:PerformedActivity.dateRange
urn:AE:Device.dateDeviceReturnedToManufacturer
bridg:PerformedActivity.dateRange
urn:C3PRv2.9:StudyParticipantDiseaseHistory.diagnosisDate
bridg:PerformedActivity.dateRange
urn:C3PRv2.9:ScheduledEpoch.startDate
bridg:PerformedActivity.dateRange
urn:C3PRv2.9:ScheduledArm.startDate
bridg:PerformedActivity.dateRange
urn:C3PRv2.9:ScheduledNotification.dateSent
bridg:PerformedActivity.dateRange
urn:C3PRv2.9:ScheduledEpoch.offEpochDate
bridg:PerformedActivity.dateRange
urn:C3PRv2.9:StudySubjectConsentVersion.informedConsentSignedDate
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:SU.SUSTDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:EX.EXENTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:EG.EGDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:SU.SUENDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:DS.DSSTTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:CM.CMENTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:EX.EXENDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:DS.DSSTDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:EG.EGTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:LB.LBDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:EX.EXSTDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:CM.CMENDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:DM.DMDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:CM.CMSTDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:VS.VSDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:PE.PETIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:VS.VSTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:CM.CMSTTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:PE.PEDAT
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:LB.LBTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:EX.EXSTTIM
bridg:PerformedActivity.dateRange
urn:CDASHv1.1:DA.DADAT
bridg:PerformedActivity.dateRange
urn:CTGOV:Record_Verification_Date
bridg:PerformedActivity.dateRange
urn:CTOM:StudyParticipantAssignment.enrollmentAge
bridg:PerformedActivity.dateRange
urn:CTOM:AdverseEventTherapy.treatmentDate
bridg:PerformedActivity.dateRange
urn:CTOM:Surgery.startDate
bridg:PerformedActivity.dateRange
urn:CTOM:Imaging.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:Radiation.startDate
bridg:PerformedActivity.dateRange
urn:CTOM:Procedure.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:SpecimenAcquisition.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:Radiation.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:Surgery.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:SubstanceAdministration.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:Activity.startDate
bridg:PerformedActivity.dateRange
urn:CTOM:SubstanceAdministration.startDate
bridg:PerformedActivity.dateRange
urn:CTOM:Imaging.startDate
bridg:PerformedActivity.dateRange
urn:CTOM:SpecimenAcquisition.startDate
bridg:PerformedActivity.dateRange
urn:CTOM:Activity.stopDate
bridg:PerformedActivity.dateRange
urn:CTOM:DeathSummary.evaluationDate
bridg:PerformedActivity.dateRange
urn:CTOM:Procedure.startDate
bridg:PerformedActivity.dateRange
urn:CTRPv1.0:ObservationalStudyProtocol.recordVerificationDate
bridg:PerformedActivity.dateRange
urn:CTRPv1.0:StudyProtocol.recordVerificationDate
bridg:PerformedActivity.dateRange
urn:CTRPv1.0:InterventionalStudyProtocol.recordVerificationDate
bridg:PerformedActivity.dateRange
urn:CTRPv3.8:PerformedActivity.actualDateRange
bridg:PerformedActivity.dateRange
urn:CTRv1.0:PerformedActivity.dateRange
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2931627:Therapies.Date_radiation_therapy_stopped:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2964208:Therapies.Specify_the_date_the_first_chemotherapy_cycle_began
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2771864:Therapies.If_the_apheresis_for_the_DCI_source_was_done_at_a_different_time_other_than_for_the_collection_of_PBSC_used_for_the_allogeneic_HSCT__what_was_the_date_of_apheresis?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2771946:Therapies.Date_of_first_leukapheresis:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2986174:Occurrences.If_necessary__please_validate_the_sample_collection_date_response.
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866435:Occurrences.Date_the_molecular_complete_remission_was_determined:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866947:Occurrences.Date_the_relapse_/_progression_was_first_seen_by_molecular_method:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2953241:Techniques.Date_of_consent_to_submit_research_data:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866766:Therapies.Date_of_product_collection:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2953362:Lab_Results.Date_the_histologic_transformation_occurred:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3061335:Therapies.What_date_was_immunotherapy_administered?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2957536:Occurrences.Date_of_secondary_malignancy:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866737:Medical_Records_and_Forms.Clinical_Data_Form_Today's_Date
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2797546:Occurrences.Date_first_discharged_from_hospital_post-HSCT:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3005937:Occurrences.Evaluation_Date:
HSCT : Part 1 of 4.Date of the most recent previous HSCT:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866424:Hematopoietic_Stem_Cell_Transplant
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866710:Diagnosis.What_is_the_diagnosis_date_of_the_new_malignancy__lymphoproliferative_or_myeloproliferative_disorder_that_occurred?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2774075:Numbers.How_many_subsequent_days_of_collection?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2770838:Occurrences.What_was_the_date_of_the_subsequent_HSCT?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866078:Occurrences.Date_platelets____20_x_10_9/L:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2786643:Occurrences.Thawing_process_begin_time:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2931619:Therapies.Date_radiation_therapy_started:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2794460:Occurrences.Actual_date_of_follow-up:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2978753:Occurrences.Date_of_post_therapy_disease_relapse/progression
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3019234:Therapies.What_date_did_the_radiation_therapy_end?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3018891:Therapies.Radiation_therapy_administered_begin_date:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866131:Occurrences.Date_the_original_disease_status_was_determined:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2965140:Procedures.Date_of_excisional_biopsy_/_surgical_procedure_performed:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3163964:Therapies.Platelet_transfusion_date:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866144:Occurrences.If_absolute_neutrophil_count_of_0.5x10_9/L_has_not_been_achieved__what_was_the_date_of_last_assessment?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866037:Procedures.Date_of_multiple_product_infusion
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2594448:Therapies.What_was_the_start_date_for_the_velafermin_administration?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2960535:Therapies.When_did_therapy_stop?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866433:Occurrences.Specify_the_date_the_clinical_/_hematologic_CR_was_achieved:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866483:Therapies.Specify_the_date_for_the_first_course_of_each_agent_administered:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2594446:Therapies.Specify_the_start_date_of_the_KGF_administration:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2960313:Therapies.When_did_the_preparative_regimen_medication_start?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2875783:Therapies.Preparative_regimen_begin_date:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866494:Lab_Results.Date_of_decline_in_ANC_to_less_than_500/mmE3_for_3_days_or_more:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2770388:Lab_Results.What_was_the_date_of_the_molecular_analysis?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866059:Lab_Results.Date_of_product_analysis:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2860472:Therapies.What_date_did_the_systemic_therapy_end?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3061478:Therapies.Specify_the_date_other_treatment_was_started:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2821465:Disease_Response.What_was_the_date_of_best_response?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2770403:Lab_Results.What_was_the_date_of_the_clinical_or_hematologic_evidence?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866527:Diagnosis.Date_of_diagnosis_of_chronic_GVHD
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866523:Therapies.Date_of_DCI:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2771948:Therapies.Date_of_last_leukapheresis:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3082352:Therapies.What_was_the_last_date_chemotherapy_was_administered?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2980873:Therapies.Date_of_orthopedic_surgery
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2953206:Techniques.Date_of_consent_to_donate_research_blood_samples:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866035:Therapies.Date_of_receipt_of_product_at_your_facility:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2979195:Therapies.What_was_the_date_of_the_last_chemotherapy_cycle?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2750854:Therapy_Results.Date_of_relapse_following_the_therapeutic_procedure:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2798743:Diagnosis.Specify_the_year_the_diagnosis_was_made:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2775861:Occurrences.What_date_was_an_initial_platelet_count_greater_than_or_equal_to_50_x_10E9/L_achieved?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3124175:Occurrences.Date_cytogenetic_status_established:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3057653:Therapies.Specify_the_date_retinoid_therapy_was_started:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866490:Occurrences.Thawing_process_begin_date:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2705511:Occurrences.Product_infusion_begin_time:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2707802:Occurrences.Product_infusion_end_time:
specimen collection date.
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3006893:Occurrences.Sample
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2947020:Involvement_and_Extent_of_Disease.Date_of_progression:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:MD_Anderson_Specific_Content:_Transplant.Day_of_infusion.
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2774708:Therapies.Time_of_receipt_of_product:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866949:Occurrences.Date_the_relapse_/_progression_was_first_seen_by_clinical_/_hematological_method:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866443:Occurrences.Date_the_cytogenetic_complete_remission_was_determined_via_conventional_cytogenetics:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2744513:Therapies.Specify_date_systemic/intrathecal_therapy_started:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866380:Occurrences.If_initial_platelets_have_not_recovered_to__20_x_10_9/L_since_HSCT__what_was_the_date_of_last_assessment?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866508:Occurrences.Date_the_current_disease_status_was_established:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3163960:Therapies.Erythrocyte_transfusion_date:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866764:Occurrences.What_assessment_date_determined_that_CR_has_not_been_achieved_from_the_HSCT?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2750705:Therapy_Results.Date_response_to_line_of_therapy_established:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2970253:Occurrences.If_necessary__please_validate_the_recurrent/progressive_disease_status_date_response.
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2794409:Therapies.What_was_the_end_date_the_immunosuppressive_agents_were_administered_to_treat_or_prevent_GVHD?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866746:Diagnosis.What_was_the_date_of_diagnosis_of_the_primary_disease_for_which_the_hematopoietic_stem_cell_transplantation_was_performed?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866759:Occurrences.Survival_status:latest_follow-up_date
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2860466:Therapies.What_date_did_the_systemic_therapy_begin?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2954767:Therapies.What_date_was_the_surgical_procedure_performed?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2936618:Occurrences.Date_the_disease_status_was_established:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_3115646:Therapies.Date_of_previous_HSCT:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866414:Occurrences.First_date_of_3_consecutive_labs_initial_ANC_recovery____to_0.5_x_10_9_was_achieved:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2744515:Therapies.Specify_date_systemic/intrathecal_therapy_ended:
HSCT : Part 1 of 4.Date of hematopoietic stem cell transplantation (HSCT for which this form is being completed:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866938:Hematopoietic_Stem_Cell_Transplant
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866951:Occurrences.First_date_seen_that_detected_the_relapse_/_progression_by_cytogenetic_/_FISH_method:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2782523:Lab_Results.What_was_the_date_of_the_cytogenetic_analysis?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866487:Activity.Date_storage_started:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866485:Lab_Results.Date_of_ANC_recovery:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2786663:Occurrences.Thawing_process_end_time:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2861238:Occurrences.When_was_the_disease_assessment_type_used_to_assess_the_disease?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2866534:Diagnosis.If_the_MDS_sub_type_is_AML__date_of_MDS_diagnosis:
bridg:PerformedActivity.dateRange
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Number_of_days_cell_product_was_in_culture
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2960533:Therapies.When_did_the_therapy_start?
bridg:PerformedActivity.dateRange
urn:HCTv1.0:CDE_2760949:Disease__Disorder_or_Finding.Date_of_the_disease_status_evaluation:
in R_Product
bridg:PerformedActivity.dateRange
urn:ICSRr2:TransportationEvent.effectiveTime
in R_Specimen universal
bridg:PerformedActivity.dateRange
urn:ICSRr2:SpecimenCollectionProcess.effectiveTime
in IndividualCaseSafetyReport
bridg:PerformedActivity.dateRange
urn:ICSRr2:RelatedInvestigation.effectiveTime
in R_Product
bridg:PerformedActivity.dateRange
urn:ICSRr2:ProductEvent.effectiveTime
in IndividualCaseSafetyReport
bridg:PerformedActivity.dateRange
urn:ICSRr2:InvestigativeEvent.effectiveTime
bridg:PerformedActivity.dateRange
urn:Lab:Activity.actualStartDateTime
bridg:PerformedActivity.dateRange
urn:Lab:LabResult.testPerformedDateTime
bridg:PerformedActivity.dateRange
urn:Lab:Activity.actualEndDateTime
bridg:PerformedActivity.dateRange
urn:LabViewer2.2:LaboratoryResult.testPerformedDateTime
bridg:PerformedActivity.dateRange
urn:LabViewer2.2:SpecimenCollection.actualEndDateTime
bridg:PerformedActivity.dateRange
urn:LabViewer2.2:Activity.actualStartDateTime
bridg:PerformedActivity.dateRange
urn:LabViewer2.2:Activity.actualEndDateTime
bridg:PerformedActivity.dateRange
urn:LabViewer2.2:SpecimenCollection.actualStartDateTime
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2004004v3.0:_Sample_Collection_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2004095v3.0:_Start_Time
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_3028744v1.0:_Intervention_Occurrence_Begin_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2746541v1.0:_Participant_Enrollment_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_3008897v1.0:_Case_Report_Form_Review_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_62739v3.0:_Current_Stage_Complete_Assessment_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_65167v3.0:_Last_Treatment_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_3028746v1.0:_Intervention_Occurrence_End_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2179659v2.0:_Patient_Relevant_Medical_History_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2993v4.0:_Treatment_Reporting_Period_Begin_Dat
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_64166v3.0:_Form_Amended_Complete_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2003580v3.0:_Lab_Collection_Time
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2992v4.0:_Treatment_Reporting_Period_End_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2171v4.0:_Patient_Registration_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2004170v3.0:_Evaluation_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2003745v5.0:_Form_Completion_Date
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2004139v3.0:_Stop_Time
bridg:PerformedActivity.dateRange
urn:NCI_CRF_Standard:CDE_2003745v5.0:_Form_Completion_Date
bridg:PerformedActivity.dateRange
urn:PSC:Occurred.date
bridg:PerformedActivity.dateRange
urn:PSC:ScheduledEventState.occured
bridg:PerformedActivity.dateRange
urn:PSC:VitalSign.measureTime
bridg:PerformedActivity.dateRange
urn:PSC:StudyParticipantAssignment.startDate
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:CO.CODTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SC.SCDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SU.SUENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:PE.PEDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:QS.QSDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:DA.DADTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:DM.DMDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SE.SESTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:LB.LBENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SV.SVSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:LB.LBDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SV.SVENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:EX.EXSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:EG.EGDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:VS.VSDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:EX.EXENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:CM.CMSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SE.SEENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:SU.SUSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:DS.DSSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:IE.IEDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:DS.DSDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.1:CM.CMENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMENRTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMSTRF
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CESTTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:VS.VSRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:QS.QSRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CESTRF
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:PP.PPRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CEENRTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMENTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CO.CODTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:PC.PCENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUSTRTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:MS.MSDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:EX.EXSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:DA.DADTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:IE.IEDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SV.SVSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:EG.EGRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUENRF
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:PP.PPDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:VS.VSDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUSENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SE.SEENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:DM.DMDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:MB.MBRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMSTRTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CEENRF
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:MB.MBDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:PC.PCDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUSTRF
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CESTRTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:EG.EGDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:LB.LBENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUENRTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CEENTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:PE.PEDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUENTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:FA.FADTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:DS.DSSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:LB.LBDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CE.CEDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:EX.EXENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SC.SCDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SE.SESTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUSTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:LB.LBRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:PC.PCRFTDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMENRF
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SV.SVENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMENDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:QS.QSDTC
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:SU.SUSTTPT
bridg:PerformedActivity.dateRange
urn:SDTM_IGv3.1.2:CM.CMSTTPT
bridg:PerformedActivity.dateRange
urn:WHO:Date_of_First_Enrollment
bridg:PerformedActivity.dateRange
urn:WHO:Date_of_Registration_in_Primary_Registry
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:TreatmentInformation.firstCourseDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:StudyParticipantConcomitantMedication.startDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:StudyParticipantConcomitantMedication.endDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:RadiationIntervention.lastTreatmentDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:Lab.labDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:SurgeryIntervention.interventionDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:AdverseEventReportingPeriod.endDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:CourseDate.date
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:MedicalDevice.explantedDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:AdverseEventReportingPeriod.startDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:ConcomitantMedication.endDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:DiseaseHistory.diagnosticDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:StudyParticipantPriorTherapy.startDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:MedicalDevice.implantedDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:ReportingPeriodReviewComment
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:AdverseEventResponseDescription.dateRemovedFromProtocol
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:AdverseEventResponseDescription.eventTreatmentTime
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:ConcomitantMedication.startDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:AdverseEventResponseDescription.reducedDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:CM.CMENTIM
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:StudyParticipantAssignment.firstCourseDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:StudyParticipantPriorTherapy.endDate
bridg:PerformedActivity.dateRange
urn:caAERSv2.2:LabValue.date
bridg:PerformedActivity.dateRangeValidationCode
dateRangeValidationCode
bridg:PerformedActivity.dateRangeValidationCode
false
bridg:PerformedActivity.dateRangeValidationCode
A coded value specifying the degree of authoritativeness or certiitude of the date of the activity
bridg:PerformedActivity.dateRangeValidationCode
date estimated
bridg:PerformedActivity.dateRangeValidationCode
date greater than 100 days - day is correct
bridg:PerformedActivity.dateRangeValidationCode
date known
bridg:PerformedActivity.dateRangeValidationCode
date less than 100 days - date is correct
bridg:PerformedActivity.dateRangeValidationCode
date previously reported
bridg:PerformedActivity.dateRangeValidationCode
The concept of "date unknown" is captured by a nullFlavor of "UNK" on the dateRange attribute, rather than a code in this attribute.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2821467:Disease_Response.If_necessary__please_validate_the_best_response_date_value.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2775854:Occurrences.If_necessary__please_validate_the_date_of_platelets_greater_than_or_equal_to_20_x_10E9/L_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_3162397:Occurrences.If_necessary__please_validate_the_last_contact_date_response
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2991134:Occurrences.If_necessary__please_validate_the_evaluation_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_3071475:Quality_of_Life.If_necessary__please_validate_the_vineland_adaptive_behavior_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2979213:Therapies.If_necessary__please_validate_the_last_chemotherapy_cycle_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_3133870:Diagnosis.If_necessary__please_validate_the_diagnosis_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2980833:Therapies.If_necessary__please_validate_the_orthopedic_surgery_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2775863:Occurrences.If_necessary__please_validate_the_date_of_platelets_greater_than_or_equal_to_50_x_10E9/L_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2946356:Occurrences.If_necessary__please_validate_the_disease_status_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2978136:Therapies.If_necessary__please_validate_the_chemotherapy_administered_date_response.
bridg:PerformedActivity.dateRangeValidationCode
urn:HCTv1.0:CDE_2794432:Therapies.If_necessary__please_validate_the_final_date_of_immunosuppressant_administration_response.
bridg:PerformedActivity.delayDuration
delayDuration
bridg:PerformedActivity.delayDuration
true
bridg:PerformedActivity.delayDuration
The period of time that an action is delayed relative to an original schedule.
bridg:PerformedActivity.delayDuration
If a substance administration is delayed 2 days as a result of an adverse event
bridg:PerformedActivity.delayDuration
then the delayDuration is 2 days.
bridg:PerformedActivity.delayDuration
Derived from comparing the dates of the scheduled activity with the corresponding performed activity.
bridg:PerformedActivity.delayDuration
urn:CTRv1.0:PerformedActivity.delayDuration
bridg:PerformedActivity.delayDuration
urn:caAERSv2.2:AdverseEventResponseDescription.daysNotGiven
bridg:PerformedActivity.delayDuration
urn:caAERSv2.2:CourseAgent.administrationDelayUnits
bridg:PerformedActivity.delayDuration
urn:caAERSv2.2:CourseAgent.administrationDelayAmount
bridg:PerformedActivity.duration
duration
bridg:PerformedActivity.duration
true
bridg:PerformedActivity.duration
The period of time over which the activity is performed.
bridg:PerformedActivity.duration
Derived from the notion of duration in the IVL (width) portion of the dateRange attribute.
bridg:PerformedActivity.duration
urn:CDASHv1.1:SU.SUCDUR
bridg:PerformedActivity.duration
urn:CDASHv1.1:SU.SUCDURU
bridg:PerformedActivity.duration
urn:CTOM:SpecimenAcquisition.durationValue
bridg:PerformedActivity.duration
urn:CTOM:Surgery.durationValue
bridg:PerformedActivity.duration
urn:CTOM:Activity.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:SpecimenAcquisition.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:Activity.durationValue
bridg:PerformedActivity.duration
urn:CTOM:Procedure.durationValue
bridg:PerformedActivity.duration
urn:CTOM:SubstanceAdministration.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:Surgery.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:SubstanceAdministration.durationValue
bridg:PerformedActivity.duration
urn:CTOM:Procedure.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:Imaging.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:Radiation.durationUnitOfMeasureCode
bridg:PerformedActivity.duration
urn:CTOM:Imaging.durationValue
bridg:PerformedActivity.duration
urn:CTOM:Radiation.durationValue
bridg:PerformedActivity.duration
urn:CTRPv3.8:PerformedActivity.actualDuration
bridg:PerformedActivity.duration
urn:CTRv1.0:PerformedActivity.duration
bridg:PerformedActivity.duration
urn:SDTM_IGv3.1.1:CM.CMDUR
bridg:PerformedActivity.duration
urn:SDTM_IGv3.1.1:EX.EXDUR
bridg:PerformedActivity.duration
urn:SDTM_IGv3.1.1:SU.SUDUR
bridg:PerformedActivity.duration
urn:SDTM_IGv3.1.2:SU.SUDUR
bridg:PerformedActivity.duration
urn:SDTM_IGv3.1.2:CM.CMDUR
bridg:PerformedActivity.duration
urn:SDTM_IGv3.1.2:EX.EXDUR
bridg:PerformedActivity.duration
urn:caAERSv2.2:CourseAgent.durationAndSchedule
bridg:PerformedActivity.fastingStatusIndicator
fastingStatusIndicator
bridg:PerformedActivity.fastingStatusIndicator
true
bridg:PerformedActivity.fastingStatusIndicator
Specifies whether the participant had abstained from eating when the specimen is obtained.
bridg:PerformedActivity.fastingStatusIndicator
Derived from the presence of a PerformedObservation ("Was the subject fasting when the specimen collection was performed?") and associated PerformedObservationResult.value (constrained to a BL with value of "true") related to a PerformedSpecimenCollection. The PerformedObservation would be related to the PerformedSpecimenCollection by both being components of the same composite activity such as a visit (DefinedSubjectActivityGroup or PlannedSubjectActivityGroup).
bridg:PerformedActivity.fastingStatusIndicator
urn:CDASHv1.1:LB.LBCOND
bridg:PerformedActivity.fastingStatusIndicator
urn:CTRv1.0:PerformedActivity.fastingStatusIndicator
bridg:PerformedActivity.fastingStatusIndicator
urn:Lab:SpecimenCollection.fastingStatus
bridg:PerformedActivity.fastingStatusIndicator
urn:LabViewer2.2:SpecimenCollection.fastingStatusIndicator
bridg:PerformedActivity.fastingStatusIndicator
urn:SDTM_IGv3.1.1:LB.LBFAST
bridg:PerformedActivity.fastingStatusIndicator
urn:SDTM_IGv3.1.2:PC.PCFAST
bridg:PerformedActivity.fastingStatusIndicator
urn:SDTM_IGv3.1.2:LB.LBFAST
bridg:PerformedActivity.medicalHistoryIndicator
medicalHistoryIndicator
bridg:PerformedActivity.medicalHistoryIndicator
true
bridg:PerformedActivity.medicalHistoryIndicator
Specifies whether the activity is considered part of the historical record of a subject, that is, it did not occur within the bounds of the study.
bridg:PerformedActivity.medicalHistoryIndicator
Derived from comparing the date range of the activity (PerformedActivity.dateRange) with the subject participation in the study (PerformedStudySubjectMilestone.studyReferenceDateRange). If the date is within the study participation date range then this indicator will be "false". Note that this means that this indicator will be derived differently for each study.
bridg:PerformedActivity.medicalHistoryIndicator
urn:HCTv1.0:CDE_2676441:Comorbid_Conditions.Is_there_a_history_of_mechanical_ventilation?
bridg:PerformedActivity.negationIndicator
negationIndicator
bridg:PerformedActivity.negationIndicator
false
bridg:PerformedActivity.negationIndicator
Specifies whether an activity did not occur.
bridg:PerformedActivity.negationIndicator
If a subject did not take aspirin in the previous week
bridg:PerformedActivity.negationIndicator
the negationIndicator = "true".
bridg:PerformedActivity.negationIndicator
If it is important to capture the fact that a particular activity did not occur, then this attribute is used, often along with negationReason.
bridg:PerformedActivity.negationIndicator
urn:AE:ProductInvestigation.investigationPerformedIndicator
bridg:PerformedActivity.negationIndicator
urn:AE:PerformedObservationResult.negationIndicator
bridg:PerformedActivity.negationIndicator
urn:CDASHv1.1:VS.VSSTAT
bridg:PerformedActivity.negationIndicator
urn:CTRv1.0:PerformedActivity.negationIndicator
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760378:Specimen_Characteristics.Was_the_cell_viability_tested?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2691376:Lab_Results.For_the_polymyositis-dermatomyositis__were_the_EMG_results_typical_of_the_disease?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2749876:Lab_Results.For_the_wegener_granulomatosis__what_was_the_result_of_the_laboratory_procedure?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073239:Lab_Results.What_is_the_reason_for_the_DQA1_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3098936:Individuals.What_is_the_reason_for_the_missing_number_of_pregnancies?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2691374:Lab_Results.For_the_dermatomyositis__was_there_a_rash_present_that_was_typical_of_the_disease?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760308:Lab_Results.Did_laboratory_procedure_test_for_CD3_+_cells?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073222:Lab_Results.What_is_the_reason_for_the_C_alleles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2686188:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_ds_DNA_test_result?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073220:Lab_Results.What_is_the_reason_for_the_B_alleles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2749870:Lab_Results.For_the_antiphospholipid_syndrome__what_was_the_result_of_the_laboratory_procedure?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2682913:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_test_results_at_diagnosis_for_the_other_antibody?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2775132:Therapies.Was_a_particular_post_hematopoietic_stem_cell_transplant_therapy_administered?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073218:Lab_Results.What_is_the_reason_for_the_A_alleles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760376:Lab_Results.Did_laboratory_procedure_test_for_CD4_+_cells?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760277:Lab_Results.Did_laboratory_procedure_test_for_nucleated_red_blood_cells?
SLE, what was the C4 test result?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2689324:Lab_Results.For_the_systemic_lupus_erythematosus
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2769662:Procedures.Did_this_donor_have_a_central_line_placed?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073228:Lab_Results.What_is_the_reason_for_the_DRB4_alleles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073224:Lab_Results.What_is_the_reason_for_the_DRB1_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073243:Lab_Results.What_is_the_reason_for_the_DPA1_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073237:Lab_Results.What_is_the_reason_for_the_DPB1_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2691365:Lab_Results.For_the_polymyositis-dermatomyositis__were_the_biopsy_results_typical_of_the_disease?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2686182:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_ANA_test_result?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2689329:Lab_Results.For_systemic_lupus__erythematosus__what_was_the_total_complement_test_result?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073235:Lab_Results.What_is_the_reason_for_the_DQB1_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760292:Lab_Results.Did_the_laboratory_procedure_test_for_CD34+_cells?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2749880:Lab_Results.For_the_polyarteritis_nodosa__classical_or_microscopic__what_was_the_laboratory_procedure_type?
NAT for human immunodeficiency virus(HIV-1 performed; specify results
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2695060:Lab_Results.If_FDA_licensed_nucleic_acid_amplification_test
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073233:Lab_Results.What_is_the_reason_for_the_DRB5_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760131:Lab_Results.Did_laboratory_procedure_test_for_mononucleated_cells?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2760264:Lab_Results.Did_laboratory_procedure_test_for_nucleated_cells?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2748995:Techniques.Was_a_particular_tumor_cell_detection_method_used_after_purging?
Chronic
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2681691:Chronic_or_Associated_Diseases_and_Exposures.What_was_the_recipient's_test_results_for_the_presence_of_CMV-antibodies?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2686194:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_C3_test_result?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2772013:Procedures.Was_the_donor_tested_for_sickle_cell_anemia?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_2682755:Therapies.Was_imatinib_mesylate_given_for_pre-transplant_therapy_for_the_other_acute_leukemia_anytime_prior_to_the_start_of_the_preparative_regimen?
bridg:PerformedActivity.negationIndicator
urn:HCTv1.0:CDE_3073226:Lab_Results.What_is_the_reason_for_the_DRB3_allelles_missing_value?
bridg:PerformedActivity.negationIndicator
urn:NCI_CRF_Standard:CDE_2838523v1.0:_Laboratory_Specimen_Collection_Status_Indicator
bridg:PerformedActivity.negationIndicator
urn:NCI_CRF_Standard:CDE_2179986v1.0:_Concomitant_Medication_Use_Ind-3
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:MH.MHSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:QS.QSSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:DA.DASTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:VS.VSSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:SU.SUSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:EG.EGSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:LB.LBSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:PE.PESTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:CM.CMSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.1:SC.SCSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:EG.EGSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:MB.MBSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:MS.MSSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:SU.SUSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:LB.LBSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:DA.DASTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:CM.CMSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:CE.CESTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:MH.MHSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:QS.QSSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:FA.FASTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:PE.PESTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:PP.PPSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:PC.PCSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:VS.VSSTAT
bridg:PerformedActivity.negationIndicator
urn:SDTM_IGv3.1.2:SC.SCSTAT
bridg:PerformedActivity.negationReason
negationReason
bridg:PerformedActivity.negationReason
false
bridg:PerformedActivity.negationReason
The text and/or code that describes why an activity did not occur.
bridg:PerformedActivity.negationReason
forgot to ask
bridg:PerformedActivity.negationReason
sample lost
bridg:PerformedActivity.negationReason
urn:AE:ProductInvestigation.notEvaluatedByManufacturerExplanation
bridg:PerformedActivity.negationReason
urn:CTRPv3.8:PerformedSubjectMilestone.missedReason
bridg:PerformedActivity.negationReason
urn:CTRv1.0:PerformedActivity.negationReason
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2556195:Therapy_Results.Specify_reason
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2949994:Therapies.What_is_the_reason_for_the_systemic_therapy_cycle_administered_missing_value?
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2775548:Therapies.Specify_the_reason_the_HSCT_was_not_performed:
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2646256:Treatment/Off-treatment_Reasons.Reasons_for_treatment_discontinuation
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2964380:Therapy_Doses.What_is_the_reason_for_the_number_of_chemotherapy_cycles_missing_values?
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2775605:Therapies.Specify_the_reason_this_HSCT_was_canceled:
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2764241:Therapies.What_is_the_reason_for_the_systemic/intrathecal_number_of_cycles_missing_value?
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_2963889:Disease__Disorder_or_Finding.Specify_reason_status_was_not_assessed:
bridg:PerformedActivity.negationReason
urn:HCTv1.0:CDE_3124485:Disease_Response.What_is_the_reason_for_the_missing_disease_status?
bridg:PerformedActivity.negationReason
urn:PSC:Canceled
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:DA.DAREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:PE.PEREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:EG.EGREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:VS.VSREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:LB.LBREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:MH.MHREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:CM.CMREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:QS.QSREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:SC.SCREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.1:SU.SUREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:LB.LBREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:PP.PPREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:FA.FAREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:QS.QSREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:VS.VSREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:PC.PCREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:MB.MBREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:EG.EGREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:MS.MSREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:SC.SCREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:CM.CMREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:PE.PEREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:MH.MHREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:SU.SUREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:DA.DAREASND
bridg:PerformedActivity.negationReason
urn:SDTM_IGv3.1.2:CE.CEREASND
bridg:PerformedActivity.repetitionNumber
repetitionNumber
bridg:PerformedActivity.repetitionNumber
true
bridg:PerformedActivity.repetitionNumber
An integer that identifies the particular occurrence of a repeating activity. The first repetition is defined as '1'.
bridg:PerformedActivity.repetitionNumber
A PlannedActivity might have a repeatQuantity of 4 which would result in 4 ScheduledActivity and PerformedActivity with repetitionNumbers of 1
bridg:PerformedActivity.repetitionNumber
2
bridg:PerformedActivity.repetitionNumber
3
bridg:PerformedActivity.repetitionNumber
and 4 respectively.
bridg:PerformedActivity.repetitionNumber
Derived from ScheduledActivity.repetitionNumber.
bridg:PerformedActivity.repetitionNumber
urn:CTRv1.0:PerformedActivity.repetitionNumber
bridg:PerformedActivity.repetitionNumber
urn:HCTv1.0:CDE_2954036:Therapy_Doses.Specify_the_number_of_days_of_radiation_therapy
bridg:PerformedActivity.repetitionNumber
urn:HCTv1.0:CDE_3060718:Therapies.What_was_the_number_of_cycles_for_the_therapeutic_procedure?
bridg:PerformedActivity.repetitionNumber
urn:HCTv1.0:CDE_3060732:Therapies.What_is_the_reason_for_the_number_of_cycles_missing_value?
bridg:PerformedActivity.repetitionNumber
urn:HCTv1.0:CDE_2763975:Therapies.What_is_the_number_of_systemic/intrathecal_therapy_cycles_administered?
bridg:PerformedActivity.repetitionNumber
urn:NCI_CRF_Standard:CDE_2744948v1.0:_Treatment_Cycle_Number
bridg:PerformedActivity.repetitionNumber
urn:NCI_CRF_Standard:CDE_62676v3.0:_Prior_Chemotherapy_Regimen_Number
bridg:PerformedActivity.repetitionNumber
urn:NCI_CRF_Standard:CDE_62590v3.0:_Agent_Course_Count
bridg:PerformedActivity.repetitionNumber
urn:NCI_CRF_Standard:CDE_2732184v1.0:_Protocol_Course_Number_Count
bridg:PerformedActivity.repetitionNumber
urn:NCI_CRF_Standard:CDE_2072v4.1:_Treatment_Current_Course_Number
bridg:PerformedActivity.repetitionNumber
urn:caAERSv2.2:CourseDate.number
bridg:PerformedActivity.repetitionNumber
urn:caAERSv2.2:TreatmentInformation.totalCourses
bridg:PerformedActivity.repetitionNumber
urn:caAERSv2.2:AdverseEventReportingPeriod.cycleNumber
bridg:PerformedActivity.statusCode
statusCode
bridg:PerformedActivity.statusCode
false
bridg:PerformedActivity.statusCode
A coded value specifying the phase in the lifecycle of a performed activity.
bridg:PerformedActivity.statusCode
For a lab test
bridg:PerformedActivity.statusCode
this would be the condition or stage in the lifecycle of the test (e.g.
bridg:PerformedActivity.statusCode
"completed"
bridg:PerformedActivity.statusCode
"canceled"
bridg:PerformedActivity.statusCode
etc.).
bridg:PerformedActivity.statusCode
Please refer to the Performed Activity Status state transition diagram for further details.
bridg:PerformedActivity.statusCode
urn:AE:PerformedActivity.ongoingPerformanceIndicator
bridg:PerformedActivity.statusCode
urn:AE:ProductInvestigation.manufacturerEvaluationStatus
bridg:PerformedActivity.statusCode
urn:CTOM:Histopathology.statusCode
bridg:PerformedActivity.statusCode
urn:CTOM:Observation.statusCode
bridg:PerformedActivity.statusCode
urn:CTOM:ClinicalResult.statusCode
bridg:PerformedActivity.statusCode
urn:CTRPv1.0:Activity.statusCode
bridg:PerformedActivity.statusCode
urn:CTRPv1.0:SubstanceAdministration.statusCode
bridg:PerformedActivity.statusCode
urn:CTRPv3.8:Activity.statusCode
bridg:PerformedActivity.statusCode
urn:CTRv1.0:PerformedActivity.statusCode
bridg:PerformedActivity.statusCode
urn:HL7SD:EligibilityCriterion.statusCode
in IndividualCaseSafetyReport
bridg:PerformedActivity.statusCode
urn:ICSRr2:RelatedInvestigation.statusCode
in IndividualCaseSafetyReport
bridg:PerformedActivity.statusCode
urn:ICSRr2:InvestigativeEvent.statusCode
bridg:PerformedActivity.statusCode
urn:Lab:LabTest.status
bridg:PerformedActivity.statusCode
urn:LabViewer2.2:LaboratoryTest.status
bridg:PerformedActivity.statusDate
statusDate
bridg:PerformedActivity.statusDate
false
bridg:PerformedActivity.statusDate
The date (and time) on which the status is assigned to the activity.
bridg:PerformedActivity.statusDate
urn:CTRPv1.0:SubstanceAdministration.statusDateRange
bridg:PerformedActivity.statusDate
urn:CTRPv1.0:Activity.statusDateRange
bridg:PerformedActivity.statusDate
urn:CTRPv3.8:Activity.statusDateRange
bridg:PerformedActivity.statusDate
urn:CTRv1.0:PerformedActivity.statusDate
bridg:PerformedActivity.statusDate
urn:LabViewer2.2:Study.startDate
bridg:PerformedActivity.studyDayRange
studyDayRange
bridg:PerformedActivity.studyDayRange
true
bridg:PerformedActivity.studyDayRange
The relative timing for a performed activity expressed as the number of days offset from the study-defined reference activity (e.g., date of registration, start of treatment) for this particular experimental unit.
bridg:PerformedActivity.studyDayRange
Day 1
bridg:PerformedActivity.studyDayRange
Days 10-20
bridg:PerformedActivity.studyDayRange
Study Day
bridg:PerformedActivity.studyDayRange
Derived from the dateRange of this activity minus the dateRange of the reference activity + 1.
The study-defined reference activity can be different from study to study. The study day for a date after this reference activity is a positive integer calculated as the difference in the two dates + 1. The study day for dates before the reference activity is a negative integer calculated as the difference between the two dates. Note that this means there is no "Day 0."
bridg:PerformedActivity.studyDayRange
urn:CTRv1.0:PerformedActivity.studyDayRange
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:AE.AEENDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:SC.SCDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:CM.CMSTDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:DS.DSSTDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:MS.MSDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:MB.MBDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:AE.AESTDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:EX.EXSTDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:DM.DMDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:FA.FADY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:SU.SUENDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:VS.VSDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:MH.MHDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:CM.CMENDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:SV.SVSTDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:PC.PCDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:EX.EXENDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:QS.QSDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:SU.SUSTDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:SV.SVENDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:DA.DADY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:IE.IEDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:PE.PEDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:LB.LBDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:CE.CEDY
bridg:PerformedActivity.studyDayRange
urn:SDTM_IGv3.1.2:EG.EGDY
bridg:PerformedAdministrativeActivity.varianceReasonCode
varianceReasonCode
bridg:PerformedAdministrativeActivity.varianceReasonCode
false
bridg:PerformedAdministrativeActivity.varianceReasonCode
A coded value specifying why what occurred is different from what was expected.
bridg:PerformedAdministrativeActivity.varianceReasonCode
Subject received early treatment because of vacation plans.
bridg:PerformedAdministrativeActivity.varianceReasonCode
urn:CTOM:StudyParticipantAssignment.eligibilityWaiverReasonText
bridg:PerformedAdministrativeActivity.varianceReasonCode
urn:CTRv1.0:PerformedAdministrativeActivity.varianceReason
bridg:PerformedAdministrativeActivity.varianceReasonCode
urn:SDTM_IGv3.1.1:DS.DSTERM
bridg:PerformedAdministrativeActivity.varianceTypeCode
varianceTypeCode
bridg:PerformedAdministrativeActivity.varianceTypeCode
false
bridg:PerformedAdministrativeActivity.varianceTypeCode
A coded value specifying the kind of variance.
bridg:PerformedAdministrativeActivity.varianceTypeCode
early / late occurrence of an act
bridg:PerformedAdministrativeActivity.varianceTypeCode
higher / lower amount transferred
bridg:PerformedAdministrativeActivity.varianceTypeCode
urn:CTRv1.0:PerformedAdministrativeActivity.varianceTypeCode
New content - variance type needed for RIM mapping
bridg:PerformedAdministrativeActivity.varianceTypeCode
urn:SDTM_IGv3.1.1:
bridg:PerformedClinicalInterpretation.abnormalIndicator
abnormalIndicator
bridg:PerformedClinicalInterpretation.abnormalIndicator
true
bridg:PerformedClinicalInterpretation.abnormalIndicator
Specifies whether an interpreted event is abnormal.
bridg:PerformedClinicalInterpretation.abnormalIndicator
Derived from PerformedClinicalInterpretation.value(ANY=>CD).code WHERE PerformedObservationResult.typeCode = "assess abnormality".
bridg:PerformedClinicalInterpretation.abnormalIndicator
urn:CTOM:ClinicalResult.normalAbnormalIndicator
bridg:PerformedClinicalInterpretation.abnormalIndicator
urn:CTRv1.0:PerformedClinicalInterpretation.abnormalIndicator
bridg:PerformedClinicalInterpretation.abnormalIndicator
urn:NCI_CRF_Standard:CDE_2841229v1.0:_Test_Result_Reference_Object_Range_Flag_Indicator
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
clinicallySignificantIndicator
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
true
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
Specifies whether a subject's clinical condition is important based on judgment.
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
Derived from PerformedClinicalInterpretation.value(ANY=>BL) WHERE PerformedClinicalInterpretation > PerformedObservation > DefinedObservation.nameCode = "assess clinical significance".
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:CDASHv1.1:VS.VSCLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:CDASHv1.1:LB.LBCLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:CDASHv1.1:PE.PECLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:CDASHv1.1:EG.EGCLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:CTOM:ClinicalResult.significanceIndicator
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:CTRv1.0:PerformedClinicalInterpretation.clinicallySignificantIndicator
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:SDTM_IGv3.1.2:VS.SUPPPVS.QNAM_VSCLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:SDTM_IGv3.1.2:PE.SUPPPE.QNAM_PECLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:SDTM_IGv3.1.2:EG.SUPPEG.QNAM_EGCLSIG
bridg:PerformedClinicalInterpretation.clinicallySignificantIndicator
urn:SDTM_IGv3.1.2:LB.SUPPLB.QNAM_LBCLSIG
bridg:PerformedClinicalInterpretation.severityCode
severityCode
bridg:PerformedClinicalInterpretation.severityCode
true
bridg:PerformedClinicalInterpretation.severityCode
A coded value specifying the intensity of the interpreted event.
bridg:PerformedClinicalInterpretation.severityCode
Moderate could be used to describe acne.
bridg:PerformedClinicalInterpretation.severityCode
Derived from PerformedClinicalInterpretation.value(ANY=>CD).code WHERE PerformedClinicalInterpretation > PerformedObservation > DefinedObservation.nameCode = "assess severity".
bridg:PerformedClinicalInterpretation.severityCode
urn:CTRv1.0:PerformedClinicalInterpretation.severityCode
bridg:PerformedClinicalInterpretation.severityCode
urn:HCTv1.0:CDE_2962140:Disease__Disorder_or_Finding.What_was_the_sensitivity_of_the_CNS_tumor_to_chemotherapy?
bridg:PerformedClinicalInterpretation.severityCode
urn:SDTM_IGv3.1.1:PE.PESEV
bridg:PerformedClinicalInterpretation.severityCode
urn:SDTM_IGv3.1.2:CE.CESEV
bridg:PerformedClinicalInterpretation.toxicityGradeCode
toxicityGradeCode
bridg:PerformedClinicalInterpretation.toxicityGradeCode
true
bridg:PerformedClinicalInterpretation.toxicityGradeCode
A coded value specifying the numeric grade for the toxicity.
bridg:PerformedClinicalInterpretation.toxicityGradeCode
Derived from PerformedClinicalInterpretation.value(ANY=>CD).code WHERE PerformedObservationResult > PerformedObservation > DefinedObservation > DefinedObservationResult.typeCode = "toxicity grade code"
Similar to Common Toxicity Criteria Toxicity Grade
bridg:PerformedClinicalInterpretation.toxicityGradeCode
urn:CTRv1.0:PerformedClinicalInterpretation.toxicityGradeCode
bridg:PerformedClinicalInterpretation.toxicityGradeCode
urn:SDTM_IGv3.1.1:LB.LBTOXGR
bridg:PerformedClinicalInterpretation.toxicityGradeCode
urn:SDTM_IGv3.1.2:LB.LBTOXGR
bridg:PerformedClinicalInterpretation.toxicityTermCode
toxicityTermCode
bridg:PerformedClinicalInterpretation.toxicityTermCode
false
bridg:PerformedClinicalInterpretation.toxicityTermCode
A coded value specifying the degree to which a substance is able to damage an exposed organism.
bridg:PerformedClinicalInterpretation.toxicityTermCode
hypocalcaemia
bridg:PerformedClinicalInterpretation.toxicityTermCode
Similar to CTC Term (short name), e.g., the National Cancer Institute's Common Toxicity Criteria terminology.
bridg:PerformedClinicalInterpretation.toxicityTermCode
urn:CTRv1.0:PerformedClinicalInterpretation.toxicityTermCode
bridg:PerformedClinicalInterpretation.toxicityTermCode
urn:SDTM_IGv3.1.1:LB.LBTOX
bridg:PerformedClinicalInterpretation.toxicityTermCode
urn:SDTM_IGv3.1.2:LB.LBTOX
bridg:PerformedClinicalResult.asCollectedIndicator
asCollectedIndicator
bridg:PerformedClinicalResult.asCollectedIndicator
false
bridg:PerformedClinicalResult.asCollectedIndicator
Specifies whether the observation is represented in the units or values as originally collected.
bridg:PerformedClinicalResult.asCollectedIndicator
A performing lab may have completed the observation or lab test using conventional units
bridg:PerformedClinicalResult.asCollectedIndicator
but the sponsor may wish to have the test reported in SI units. This flag will be set to "true" on the lab test that has the original units
bridg:PerformedClinicalResult.asCollectedIndicator
and "false" on the lab test in which the units that are different than the lab test's original units.
bridg:PerformedClinicalResult.asCollectedIndicator
urn:CTRv1.0:PerformedClinicalResult.asCollectedIndicator
bridg:PerformedClinicalResult.asCollectedIndicator
urn:SDTM_IGv3.1.1:LB.LBORRES
bridg:PerformedClinicalResult.biomarkerIndicator
biomarkerIndicator
bridg:PerformedClinicalResult.biomarkerIndicator
false
bridg:PerformedClinicalResult.biomarkerIndicator
Specifies whether a result is considered a biomarker.
bridg:PerformedClinicalResult.biomarkerIndicator
This attribute is based on a result as stated in the NCI Thesaurus for Biomarker: A variation in cellular or biochemical components or processes, structures, or functions that is objectively measurable in a biological system and that characterizes normal biologic processes, pathogenic processes, an organism's state of health or disease, likelihood of developing a disease, prognosis, or response to a particular therapeutic intervention. Biomarkers include but not limited to such phenotypic parameters as specific enzyme or hormone concentration, specific gene phenotype, presence or absence of biological substances.
bridg:PerformedClinicalResult.biomarkerIndicator
urn:CTOM:ClinicalResult.biomarkerIndicator
bridg:PerformedClinicalResult.biomarkerIndicator
urn:CTRv1.0:PerformedClinicalResult.biomarkerIndicator
bridg:PerformedClinicalResult.infectiousAgent
infectiousAgent
bridg:PerformedClinicalResult.infectiousAgent
true
bridg:PerformedClinicalResult.infectiousAgent
The name of the specific microbe that the test is intended to identify.
bridg:PerformedClinicalResult.infectiousAgent
streptococcus pneumoniae
bridg:PerformedClinicalResult.infectiousAgent
staphylococcus aureus
bridg:PerformedClinicalResult.infectiousAgent
Derived from PerformedObservation directly or indirectly linked to DefinedActivity.nameCode(CD).originaltext.
bridg:PerformedClinicalResult.infectiousAgent
urn:CTRv1.0:PerformedClinicalResult.infectiousAgent
bridg:PerformedClinicalResult.infectiousAgent
urn:caAERSv2.2:Lab.infectiousAgent
bridg:PerformedClinicalResult.normalRangeComparisonCode
normalRangeComparisonCode
bridg:PerformedClinicalResult.normalRangeComparisonCode
true
bridg:PerformedClinicalResult.normalRangeComparisonCode
A coded value specifying the relationship of a value to a normal range or reference range of values.
bridg:PerformedClinicalResult.normalRangeComparisonCode
high
bridg:PerformedClinicalResult.normalRangeComparisonCode
low
bridg:PerformedClinicalResult.normalRangeComparisonCode
within normal range
bridg:PerformedClinicalResult.normalRangeComparisonCode
outside normal range
bridg:PerformedClinicalResult.normalRangeComparisonCode
Derived from comparing PerformedObservationResult.value to the ReferenceResult.value.
bridg:PerformedClinicalResult.normalRangeComparisonCode
urn:CDASHv1.1:LB.LBNRIND
bridg:PerformedClinicalResult.normalRangeComparisonCode
urn:CTRv1.0:PerformedClinicalResult.normalRangeComparisonCode
bridg:PerformedClinicalResult.normalRangeComparisonCode
urn:SDTM_IGv3.1.1:VS.VSNRIND
bridg:PerformedClinicalResult.normalRangeComparisonCode
urn:SDTM_IGv3.1.1:EG.EGNRIND
bridg:PerformedClinicalResult.normalRangeComparisonCode
urn:SDTM_IGv3.1.1:LB.LBNRIND
bridg:PerformedClinicalResult.normalRangeComparisonCode
urn:SDTM_IGv3.1.2:LB.LBNRIND
bridg:PerformedClinicalResult.statusCode
statusCode
bridg:PerformedClinicalResult.statusCode
false
bridg:PerformedClinicalResult.statusCode
A coded value specifying the phase in the lifecycle of the reported result.
bridg:PerformedClinicalResult.statusCode
preliminary
bridg:PerformedClinicalResult.statusCode
final
bridg:PerformedClinicalResult.statusCode
corrected
bridg:PerformedClinicalResult.statusCode
urn:CTRv1.0:PerformedClinicalResult.statusCode
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2861133:Lab_Results.What_was_the_status_of_the_plasma_cells_in_bone_marrow_from_an_unknown_source_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2952875:Lab_Results.What_was_the_status_of_the_urinary_monoclonal_light_chain_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_3061547:Lab_Results.What_was_the_status_of_the_serum_alpha-fetoprotein_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2940075:Lab_Results.What_was_the_status_of_the_neutrophil_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2953864:Lab_Results.What_was_the_status_of_the_lactate_dehydrogenase_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2863186:Lab_Results.What_was_the_status_of_the_hematocrit_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2952919:Lab_Results.What_was_the_status_of_the_serum_free_light_chains_lambda_finding?
kappa finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2952889:Lab_Results.What_was_the_status_of_the_serum_free_light_chains
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2863877:Lab_Results.What_was_the_status_of_the_serum_ferritin_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2963402:Lab_Results.What_was_the_status_of_the_lymphocytes_present_in_bone_marrow_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2934447:Lab_Results.What_was_the_status_of_the_blasts_in_bone_marrow_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2970736:Lab_Results.What_was_the_status_of_the_expression_of_proto-oncogenes_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2861054:Lab_Results.What_was_the_status_of_the_serum_beta_2_microglobulin_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2861065:Lab_Results.What_was_the_status_of_the_serum_albumin_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2986015:Lab_Results.What_was_the_low_stroma_histology_type?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2970731:Lab_Results.What_was_the_status_of_the_TRK_expression_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2866061:Lab_Results.What_was_the_status_of_the_cerebrospinal_fluid_total_protein_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2884436:Lab_Results.What_was_the_status_of_the_lymphocytes_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2895879:Lab_Results.What_was_the_status_of_the_eosinophil_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2957563:Lab_Results.HER2_IHC_Status
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2897741:Lab_Results.What_was_the_status_of_the_basophil_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2974094:Lab_Results.What_was_the_status_of_the_gamma-enolase_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2953017:Lab_Results.What_was_the_status_of_the_serum_monoclonal_M_protein_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2967117:Lab_Results.What_was_the_status_of_the_homovanillic_acid_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2969525:Lab_Results.What_was_the_status_of_the_vanillyl_mandelic_acid_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_3061552:Lab_Results.What_was_the_status_of_the_serum_beta-human_chorionic_gonadotropin_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2963488:Lab_Results.What_was_the_status_of_the_prolymphocytes_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2954073:Lab_Results.What_was_the_status_of_the_serum_immunologic_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_3019776:Lab_Results.What_was_the_status_of_the_modal_chromosome_number_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2982913:Lab_Results.What_was_the_status_of_the_uncorrected_reticulocyte_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2860841:Lab_Results.What_was_the_status_of_the_platelet_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2860929:Lab_Results.What_was_the_status_of_the_blood_blast_count_finding?
bridg:PerformedClinicalResult.statusCode
urn:HCTv1.0:CDE_2970537:Lab_Results.What_was_the_status_of_the_N-myc_amplification_finding?
bridg:PerformedClinicalResult.statusCode
urn:Lab:LabResult.reportedResultStatus
bridg:PerformedClinicalResult.statusCode
urn:LabViewer2.2:LaboratoryResult.reportedResultStatus
bridg:PerformedClinicalResult.targetBiomarkerCode
targetBiomarkerCode
bridg:PerformedClinicalResult.targetBiomarkerCode
false
bridg:PerformedClinicalResult.targetBiomarkerCode
A coded value specifying a variation in cellular or biochemical components or processes, structures, or functions that is objectively measurable in a biological system and that characterizes normal biologic processes, pathogenic processes, an organism's state of health or disease, likelihood of developing a disease, prognosis, or response to a particular therapeutic intervention. This is the focus of an observation.
bridg:PerformedClinicalResult.targetBiomarkerCode
Biomarkers include but are not limited to such phenotypic parameters as specific enzyme or hormone concentration
bridg:PerformedClinicalResult.targetBiomarkerCode
specific gene phenotype
bridg:PerformedClinicalResult.targetBiomarkerCode
presence or absence of biological substance.
bridg:PerformedClinicalResult.targetBiomarkerCode
For an observation with a nameCode of "Determine the Allele for the HLA-A Locus on Chromosome 6"
bridg:PerformedClinicalResult.targetBiomarkerCode
the observation result might have a targetBiomarkerCode of "HLA-A" and a value of "HLA-A*01:01:01" (the specific allele)
bridg:PerformedClinicalResult.targetBiomarkerCode
For an observation with a nameCode of "Determine the variant nucleotide for Single Nucleotide Polymorphism RS110789"
bridg:PerformedClinicalResult.targetBiomarkerCode
the observation result might have a targetBiomarkerCode of "Rs110789" and a value of "C" (cytosine
bridg:PerformedClinicalResult.targetBiomarkerCode
the specific nucleotide that is variant)
bridg:PerformedClinicalResult.targetBiomarkerCode
Genetic Marker
bridg:PerformedClinicalResult.targetBiomarkerCode
There is no associated 'approach' for a Biomarker, as there is for an anatomic site. In the context of Bone Marrow Transplantation, the bodily substance that is collected to determine the Biomarker (the HLA Alleles) is typically blood or saliva. Thus, the thing that is collected is the typeCode of the Material that is collected via a PerformedSpecimenCollection.
The attribute 'targetBiomarkerCode' was chosen as inclusive of 'targetGeneticMarkerCode', which is more specific to the Bone Marrow Transplantation domain. However, the Life Sciences Domain Analysis Model is using Biomarker as the focus of their Genomic Analysis, and thus this broader definition was chosen to facilitate that alignment.
bridg:PerformedDiagnosis.bodySystemCode
bodySystemCode
bridg:PerformedDiagnosis.bodySystemCode
false
bridg:PerformedDiagnosis.bodySystemCode
A coded value specifying the anatomical structure that consists of organs and organ subclasses responsible for certain body functions.
bridg:PerformedDiagnosis.bodySystemCode
gastrointestinal system
bridg:PerformedDiagnosis.bodySystemCode
urinary system
bridg:PerformedDiagnosis.bodySystemCode
hematopoietic system
bridg:PerformedDiagnosis.bodySystemCode
urn:HCTv1.0:CDE_3082348:Involvement_and_Extent_of_Disease.What_was_the_site_of_extranodal_involvement?
bridg:PerformedDiagnosis.diseaseStatusCode
diseaseStatusCode
bridg:PerformedDiagnosis.diseaseStatusCode
false
bridg:PerformedDiagnosis.diseaseStatusCode
A coded value specifying the amount of disease present in a subject.
bridg:PerformedDiagnosis.diseaseStatusCode
metastatic and disease-free (cancer-specific examples)
bridg:PerformedDiagnosis.diseaseStatusCode
urn:CTOM:Diagnosis.diseaseSatusCode
bridg:PerformedDiagnosis.diseaseStatusCode
urn:CTRv1.0:PerformedDiagnosis.diseaseStatusCode
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2685079:Disease_Response.What_was_the_status_of_the_hodgkin_lymphoma_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2685098:Disease_Response.What_was_the_status_of_the_other_acute_leukemia_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3008113:Disease_Response.Specify_the_best_cardiac_response:
CML: Part 1 of 2.If the CML was in hematologic complete remission, what was the disease status before treatment?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2675153:Chronic_Myelogenous_Leukemia
Karnofsky
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2003853:Quality_of_Life.Performance_Status
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2962154:Disease__Disorder_or_Finding.What_was_the_CNS_disease_status?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2965947:Disease__Disorder_or_Finding.What_is_the_status_of_the_original_disease?_
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2685083:Disease_Response.What_was_the_status_of_the_non-hodgkin's_lymphoma_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3009297:Disease_Response.Specify_other_system_best_response:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3029363:Disease_Response.What_is_the_Chronic_Lymphocytic_Leukemia_best_response_type?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3130146:Disease_Response.What_was_the_chronic_lymphocytic_leukemia_status?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2947820:Disease__Disorder_or_Finding.What_was_the_plasma_cell_disorder_disease_status?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2950554:Disease_Response.What_was_the_best_response_to_HSCT?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3008793:Disease__Disorder_or_Finding.Specify_the_status_of_autonomic_neuropathy:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2970355:Disease_Response.What_was_breast_cancer_best_response?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2939779:Disease__Disorder_or_Finding.What_was_the_status_of_the_myelofibrosis?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2686057:Myelodysplastic_or_Myeloproliferative_Disease_Classification_at_Diagnosis.If_the_MDS/MPS/CMML_was_treated_with_chemotherapy__what_was_the_disease_status_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2954551:Disease_Response.What_was_the_best_response_of_the_CNS_neoplasm?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2677309:Involvement_and_Extent_of_Disease.Specify_other_main_cause_of_death:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2688889:Disease_Response.What_was_the_status_of_the_other_leukemia_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3008833:Disease_Response.Specify_the_best_response_of_peripheral_neuropathy:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2971700:Disease_Response.Specify_the_disease_status:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3073181:Disease_Response.What_is_the_status_of_Acute_Lymphoblastic_Leukemia_?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3008778:Disease_Response.Specify_the_best_response_of_autonomic_neuropathy:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2688824:Disease_Response.At_the_time_of_transplantation__what_was_the_status_of_the_JMML?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2688964:Disease_Response.What_was_the_status_of_the_other_malignancy_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3124457:Disease_Response.Specify_the_disease_status:_
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3072091:Disease_Response.What_is_the_disease_status_of_AML_prior_to_the_prep_regimen?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3045387:Disease_Response.What_was_the_best_non-bone_response?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2980437:Disease_Response.What_was_testicular_neoplasm_the_best_response_type?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3009333:Disease__Disorder_or_Finding.Specify_the_status_of_this_system:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_58250//:Therapy_Results.Did_the_patient_achieve_a_complete_response_according_to_clinical/_hematologic_criteria
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2970628:Involvement_and_Extent_of_Disease.What_was_the_breast_carcinoma_status?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3045394:Disease_Response.What_was_the_best_bone_response?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2677716:Involvement_and_Extent_of_Disease.Main_cause_of_death:_Other_specify
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2680980:Outcome_of_Therapy.Maximum_grade_of_Acute_Graft_Versus_Host_Disease_after_this_DCI?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3009221:Disease_Response.Specify_the_best_renal_response:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2936606:Disease__Disorder_or_Finding.What_is_the_disease_status?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3008835:Disease__Disorder_or_Finding.Specify_the_status_of_peripheral_neuropathy:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2750703:Disease_Response.Best_response_to_line_of_therapy:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2936640:Disease_Response.What_was_the_best_response_of_myelodysplastic/myeloproliferative_disease_to_HSCT?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3057354:Disease__Disorder_or_Finding.Specify_current_neurologic_status:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2986871:Disease__Disorder_or_Finding.What_was_the_disease_status?_
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2770757:Disease_Response.What_was_the_recipient's_disease_status?
CML: Part 1 of 2.What was the phase of the CML at the time of transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2676471:Chronic_Myelogenous_Leukemia
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2939328:Disease_Response.Specify_cytogenetic_remission:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2691339:Disease_Response.What_was_the_plasma_cell_disorder_status_at_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2688951:Disease_Response.What_was_the_status_of_the_breast_cancer_at_the_time_of_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3076261:Disease_Response.What_was_the_disease_status?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2939802:Disease__Disorder_or_Finding.What_was_the_status_of_the_chronic_myelogenous_leukemia?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3009205:Disease_Response.Specify_the_best_hematologic_response:
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3124484:Disease_Response.What_was_the_status_of_myelodysplastic/myeloproliferative_disease?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2674599:Disease_Response.What_was_the_status_of_MDS/MPS/CMML_at_transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2957272:Disease__Disorder_or_Finding.What_was_the_status_of_lymphoma?
Lansky
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2180158:Quality_of_Life.Performance_Status
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2950694:Disease_Response.What_was_the_best_response_of_the_lymphoma_to_HSCT_?
AML or acute nonlymphocytic leukemia (ANLL at the time of transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2685090:Disease_Response.What_was_the_status_of_the_acute_myelogenous_leukemia
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_3008178:Disease_Response.Specify_the_best_hepatic_response:
ALL at the time of transplantation?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2685094:Disease_Response.What_was_the_status_of_the_acute_lymphoblastic_leukemia
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2984453:Disease_Response.What_was_the_testicular_germ_cell_cancer_best_response?
bridg:PerformedDiagnosis.diseaseStatusCode
urn:HCTv1.0:CDE_2770281:Disease_Response.What_is_the_status_of_the_original_disease?
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
diseaseStatusMissingReasonCode
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
false
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
A coded value specifying why a disease status is missing.
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
"the sample was damaged" is a reason code within the "unevaluable" classification.
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
The distinctions between unevaluable, missing reason and not assessed, will be made in the hierarchy of the reason codes and need not be made as distinct attributes, since they are mutually exclusive.
This value should only be populated if PerformedDiagnosis.diseaseStatusCode is null.
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
urn:HCTv1.0:CDE_2740336:Occurrences.If_necessary__please_validate_the_clinical_and_or_hematologic_CR_date_response:
bridg:PerformedDiagnosis.diseaseStatusMissingReasonCode
urn:HCTv1.0:CDE_2974029:Disease_Response.Specify_reason_disease_status_was_unevaluable:
bridg:PerformedDiagnosis.recurrenceIndicator
recurrenceIndicator
bridg:PerformedDiagnosis.recurrenceIndicator
false
bridg:PerformedDiagnosis.recurrenceIndicator
Specifies whether this is a reappearance of the existing disease.
bridg:PerformedDiagnosis.recurrenceIndicator
urn:CTOM:Diagnosis.recurrenceIndicator
bridg:PerformedDiagnosis.recurrenceIndicator
urn:CTRv1.0:PerformedDiagnosis.recurrenceIndicator
bridg:PerformedDiagnosisProcedureRelationship.primaryIndicator
primaryIndicator
bridg:PerformedDiagnosisProcedureRelationship.primaryIndicator
false
bridg:PerformedDiagnosisProcedureRelationship.primaryIndicator
Specifies whether this is the main or principal diagnosis addressed by a procedure.
bridg:PerformedEligibilityCriterion.displayOrder
displayOrder
bridg:PerformedEligibilityCriterion.displayOrder
false
bridg:PerformedEligibilityCriterion.displayOrder
The sequence or position of a component in a list of question or data items.
bridg:PerformedEligibilityCriterion.displayOrder
urn:CTRv1.0:PerformedEligibilityCriterion.displayOrder
bridg:PerformedEligibilityCriterion.notApplicableIndicator
notApplicableIndicator
bridg:PerformedEligibilityCriterion.notApplicableIndicator
false
bridg:PerformedEligibilityCriterion.notApplicableIndicator
Specifies whether the specific eligibility criterion is not applicable to this participant.
bridg:PerformedEligibilityCriterion.notApplicableIndicator
urn:C3PR:EligbilityCriterion.notApplicableIndicator
bridg:PerformedEligibilityCriterion.notApplicableIndicator
urn:CTRv1.0:PerformedEligibilityCriterion.notApplicableIndicator
bridg:PerformedHistopathology.differentiationGradeCode
differentiationGradeCode
bridg:PerformedHistopathology.differentiationGradeCode
false
bridg:PerformedHistopathology.differentiationGradeCode
A coded value specifying the degree of cellular differentiation in a tissue sample.
bridg:PerformedHistopathology.differentiationGradeCode
A brain tumor could be grade 3
bridg:PerformedHistopathology.differentiationGradeCode
urn:CTOM:HistopathologyGrade.gradeCode
bridg:PerformedHistopathology.differentiationGradeCode
urn:CTOM:HistopathologyGrade.gradeCodeSystem
bridg:PerformedHistopathology.differentiationGradeCode
urn:CTRv1.0:PerformedHistopathology.differentiationGradeCode
bridg:PerformedHistopathology.involvedSurgicalMarginIndicator
involvedSurgicalMarginIndicator
bridg:PerformedHistopathology.involvedSurgicalMarginIndicator
false
bridg:PerformedHistopathology.involvedSurgicalMarginIndicator
Specifies whether the margins of surgical resection are infiltrated by the abnormal tissue.
bridg:PerformedHistopathology.involvedSurgicalMarginIndicator
urn:CTOM:Histopathology.involvedSurgicalMarginIndicator
bridg:PerformedHistopathology.involvedSurgicalMarginIndicator
urn:CTRv1.0:PerformedHistopathology.involvedSurgicalMarginIndicator
bridg:PerformedImaging.contrastAgentEnhancementIndicator
contrastAgentEnhancementIndicator
bridg:PerformedImaging.contrastAgentEnhancementIndicator
false
bridg:PerformedImaging.contrastAgentEnhancementIndicator
Specifies whether the image is enhanced by the use of a contrast agent.
bridg:PerformedImaging.contrastAgentEnhancementIndicator
urn:CTOM:Imaging.contrastAgentEnhancementIndicator
bridg:PerformedImaging.contrastAgentEnhancementIndicator
urn:CTRv1.0:PerformedImaging.contrastAgentEnhancementIndicator
bridg:PerformedImaging.enhancementDescription
enhancementDescription
bridg:PerformedImaging.enhancementDescription
false
bridg:PerformedImaging.enhancementDescription
The textual representation for how an image is enhanced either physically or electronically.
bridg:PerformedImaging.enhancementDescription
urn:CTOM:Imaging.enhancementDescriptionText
bridg:PerformedImaging.enhancementDescription
urn:CTRv1.0:PerformedImaging.enhancementDescription
bridg:PerformedImaging.enhancementRate
enhancementRate
bridg:PerformedImaging.enhancementRate
false
bridg:PerformedImaging.enhancementRate
The numeric value to indicate an increase in voxel signal over time for an MRI, expressed as signal intensity units per second.
bridg:PerformedImaging.enhancementRate
urn:CTOM:Imaging.enhancementRateValue
bridg:PerformedLesionDescription.appearanceTypeCode
appearanceTypeCode
bridg:PerformedLesionDescription.appearanceTypeCode
false
bridg:PerformedLesionDescription.appearanceTypeCode
A coded value specifying the appearance of a superficial lesion.
bridg:PerformedLesionDescription.appearanceTypeCode
flat
bridg:PerformedLesionDescription.appearanceTypeCode
nodular
bridg:PerformedLesionDescription.appearanceTypeCode
urn:CTOM:LesionDescription.appearanceTypeCode
bridg:PerformedLesionDescription.appearanceTypeCode
urn:CTRv1.0:PerformedLesionDescription.appearanceTypeCode
bridg:PerformedLesionDescription.contactAnatomicSiteCode
contactAnatomicSiteCode
bridg:PerformedLesionDescription.contactAnatomicSiteCode
false
bridg:PerformedLesionDescription.contactAnatomicSiteCode
A coded value specifying the anatomic site (single) in contact with the lesion.
bridg:PerformedLesionDescription.contactAnatomicSiteCode
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:PerformedLesionDescription.contactAnatomicSiteCode
urn:CTOM:LesionDescription.contactAnatomicSiteCode
bridg:PerformedLesionDescription.contactAnatomicSiteCode
urn:CTOM:LesionDescription.contactAnatomicSiteCodeSystem
bridg:PerformedLesionDescription.contactAnatomicSiteCode
urn:CTRv1.0:PerformedLesionDescription.contactAnatomicSiteCode
bridg:PerformedLesionDescription.dimensionProduct
dimensionProduct
bridg:PerformedLesionDescription.dimensionProduct
true
bridg:PerformedLesionDescription.dimensionProduct
The result or product of multiplying dimensions (2 or 3) of a site or specimen.
bridg:PerformedLesionDescription.dimensionProduct
Derived from multiplying at least two (2) of the following: PerformedLesionDescription.xDimension, PerformedLesionDescription.yDimension, PerformedLesionDescription.zDimension.
bridg:PerformedLesionDescription.dimensionProduct
urn:CTOM:LesionDescription.dimensionProduct
bridg:PerformedLesionDescription.dimensionProduct
urn:CTRv1.0:PerformedLesionDescription.dimensionProduct
bridg:PerformedLesionDescription.dimensionProduct
urn:HCTv1.0:CDE_2963625:Surgical_Margin_Measurements.Size_of_residual_tumor_after_surgery:
bridg:PerformedLesionDescription.dimensionProduct
urn:HCTv1.0:CDE_2978340:Tumor_Measurements.What_is_the_value_of_the_primary_neoplasm_size_specimen_measurement?
bridg:PerformedLesionDescription.dimensionProduct
urn:HCTv1.0:CDE_3104035:Involvement_and_Extent_of_Disease.Specify_the_size_of_the_largest_lymph_nodal_mass:
bridg:PerformedLesionDescription.lesionNumber
lesionNumber
bridg:PerformedLesionDescription.lesionNumber
false
bridg:PerformedLesionDescription.lesionNumber
The integer assigned to a lesion for a subject.
bridg:PerformedLesionDescription.lesionNumber
Once a lesion number is designated for a specific lesion that number may not change or re-used to denote a different lesion.
bridg:PerformedLesionDescription.lesionNumber
urn:CTOM:LesionDescription.lesionNumber
bridg:PerformedLesionDescription.lesionNumber
urn:CTOM:LesionDescription.evaluationNumber
bridg:PerformedLesionDescription.lesionNumber
urn:CTRv1.0:PerformedLesionDescription.lesionNumber
bridg:PerformedLesionDescription.measurableIndicator
measurableIndicator
bridg:PerformedLesionDescription.measurableIndicator
false
bridg:PerformedLesionDescription.measurableIndicator
Specifies whether a lesion or site of disease is measurable.
bridg:PerformedLesionDescription.measurableIndicator
urn:CTOM:LesionDescription.measurableIndicator
bridg:PerformedLesionDescription.measurableIndicator
urn:CTRv1.0:PerformedLesionDescription.measurableIndicator
bridg:PerformedLesionDescription.measurableIndicator
urn:HCTv1.0:CDE_2978313:Tumor_Measurements.Was_the_primary_neoplasm_size_known?
bridg:PerformedLesionDescription.xDimension
xDimension
bridg:PerformedLesionDescription.xDimension
false
bridg:PerformedLesionDescription.xDimension
The measurement of a lesion or location in the 'X' (first or length) dimension.
bridg:PerformedLesionDescription.xDimension
This is the longest measurement or largest value if only one measurement is captured.
bridg:PerformedLesionDescription.xDimension
urn:CTOM:LesionDescription.xaDimension
bridg:PerformedLesionDescription.xDimension
urn:CTRv1.0:PerformedLesionDescription.xDimension
bridg:PerformedLesionDescription.yDimension
yDimension
bridg:PerformedLesionDescription.yDimension
false
bridg:PerformedLesionDescription.yDimension
The measurement of a lesion in the 'Y' (second or width) dimension.
bridg:PerformedLesionDescription.yDimension
urn:CTOM:LesionDescription.yaDimension
bridg:PerformedLesionDescription.yDimension
urn:CTRv1.0:PerformedLesionDescription.yDimension
bridg:PerformedLesionDescription.zDimension
zDimension
bridg:PerformedLesionDescription.zDimension
false
bridg:PerformedLesionDescription.zDimension
The measurement of a lesion in the 'Z' (third) dimension.
bridg:PerformedLesionDescription.zDimension
urn:CTOM:LesionDescription.zaDimension
bridg:PerformedLesionDescription.zDimension
urn:CTRv1.0:PerformedLesionDescription.zDimension
bridg:PerformedMaterialProcessStep.standardTimeIndicator
standardTimeIndicator
bridg:PerformedMaterialProcessStep.standardTimeIndicator
false
bridg:PerformedMaterialProcessStep.standardTimeIndicator
Specifies whether the time of the process step is specified using standard (as opposed to daylight savings) time.
bridg:PerformedMaterialProcessStep.standardTimeIndicator
If the location and date are known, this data is derivable.
bridg:PerformedMaterialProcessStep.standardTimeIndicator
urn:HCTv1.0:CDE_2786665:Occurrences.Is_the_thawing_end_time_standard_time_or_daylight_savings_time?
bridg:PerformedMaterialProcessStep.standardTimeIndicator
urn:HCTv1.0:CDE_2786645:Occurrences.Is_the_thawing_begin_time_standard_time_or_daylight_savings_time?
bridg:PerformedMaterialStorage.methodCode
methodCode
bridg:PerformedMaterialStorage.methodCode
false
bridg:PerformedMaterialStorage.methodCode
A coded value specifying the technique that is used to store the material.
bridg:PerformedMaterialStorage.methodCode
liquid nitrogen
bridg:PerformedMaterialStorage.methodCode
vapor phase
bridg:PerformedMaterialStorage.methodCode
electric freezer
bridg:PerformedMaterialStorage.methodCode
urn:HCTv1.0:CDE_2786006:Activity.Specify_the_storage_method_used_for_the_cord_blood_unit:
bridg:PerformedMaterialStorage.temperatureRange
temperatureRange
bridg:PerformedMaterialStorage.temperatureRange
false
bridg:PerformedMaterialStorage.temperatureRange
The thermal reading at which the storage unit was set.
bridg:PerformedMaterialStorage.temperatureRange
>= -80 degrees celsius
bridg:PerformedMaterialStorage.temperatureRange
-135 to -80 degrees celsius
bridg:PerformedMaterialStorage.temperatureRange
-150 to -135 degrees celsius
bridg:PerformedMaterialStorage.temperatureRange
< -150 degrees celsius
bridg:PerformedMaterialStorage.temperatureRange
urn:HCTv1.0:CDE:2786019:Activity.What_is_the_temperature_in_celsius_during_storage?
bridg:PerformedMedicalConditionResult.clinicallySignificantIndicator
clinicallySignificantIndicator
bridg:PerformedMedicalConditionResult.clinicallySignificantIndicator
true
bridg:PerformedMedicalConditionResult.clinicallySignificantIndicator
Specifies whether a subject's clinical condition is important based on judgment.
bridg:PerformedMedicalConditionResult.clinicallySignificantIndicator
Derived from PerformedClinicalInterpretation.value(ANY=> BL) WHERE PerformedClinicalInterpretation > PerformedObservation > DefinedObservation.nameCode = "assess clinical significance".
bridg:PerformedMedicalConditionResult.clinicallySignificantIndicator
urn:HCTv1.0:CDE_2759600:Diagnosis.Was_there_a_coexisting_significant_hemorrhage?
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
endRelativeToReferenceCode
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
false
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
A coded value specifying the end of the medical condition event with respect to the sponsor-defined reference period.
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
before
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
during
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
during/after
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
after
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
Derived from comparing PerformedSubstanceAdministration.dateRange(IVL<TS.DATETIME>).high and PerformedStudySubjectMilestone.studyReferenceDateRange.
Sponsors should define the reference period in the study metadata.
This may be populated when a start date is not collected.
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
urn:CTRv1.0:PerformedMedicalConditionResult.endRelativeToReferenceCode
bridg:PerformedMedicalConditionResult.endRelativeToReferenceCode
urn:SDTM_IGv3.1.1:MH.MHENRF
bridg:PerformedMedicalConditionResult.medicalHistoryIndicator
medicalHistoryIndicator
bridg:PerformedMedicalConditionResult.medicalHistoryIndicator
true
bridg:PerformedMedicalConditionResult.medicalHistoryIndicator
Specifies whether the condition is considered part of the historical record of a subject, that is, it did not occur within the bounds of the study.
bridg:PerformedMedicalConditionResult.medicalHistoryIndicator
Derived from the medical history indicator on the activity (PerformedActivity.medicalHistoryIndicator) which produced this result.
bridg:PerformedMedicalConditionResult.medicalHistoryIndicator
urn:CTRv1.0:PerformedMedicalConditionResult.medicalHistoryIndicator
bridg:PerformedMedicalConditionResult.medicalHistoryIndicator
urn:SDTM_IGv3.1.2:MH.DOMAIN
bridg:PerformedMedicalConditionResult.occurrenceDateRange
occurrenceDateRange
bridg:PerformedMedicalConditionResult.occurrenceDateRange
false
bridg:PerformedMedicalConditionResult.occurrenceDateRange
The date and time span in which the medical condition began and ended.
bridg:PerformedMedicalConditionResult.occurrenceDateRange
Onset date
bridg:PerformedMedicalConditionResult.occurrenceDateRange
resolution date
bridg:PerformedMedicalConditionResult.occurrenceDateRange
duration.
bridg:PerformedMedicalConditionResult.occurrenceDateRange
These may be partial dates or durations (duration is the width property of the IVL<TS> datatype).
A condition may be considered to have ended when a subject returns to their baseline state.
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:CDASHv1.1:MH.MHENDAT
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:CDASHv1.1:MH.MHSTDAT
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:CTRv1.0:PerformedMedicalConditionResult.occurrenceDateRange
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:HCTv1.0:CDE_2871898:Occurrences.Date_fungal_infection_occurred
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:HCTv1.0:CDE_2787854:Adverse_Events.Date_engraftment_syndrome_occurred:
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:HCTv1.0:CDE_2960491:Adverse_Events.Date_of_graft_failure:
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:NCI_CRF_Standard:CDE_2736881v1.0:_Personal_Medical_History_Ongoing_Indicator
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.1:MH.MHSTDTC
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.1:MH.MHENDTC
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.2:MH.MHENRF
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.2:CE.CESTDTC
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.2:MH.MHENDTC
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.2:CE.CEENDTC
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.2:MH.MHSTDTC
bridg:PerformedMedicalConditionResult.occurrenceDateRange
urn:SDTM_IGv3.1.2:MH.MHENRTPT
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
occurrenceDateRangeValidationCode
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
false
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
A coded value specifying the degree of authoritativeness or certitude of the occurrence date.
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
"date estimated"
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
"date > 100 days
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
date is correct"
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
"date < 100 days
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
date is correct"
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
The concept of "date unknown" is captured by a nullFlavor of "UNK" on the dateRange attribute, rather than a code in this attribute.
A patient might have recovered from neutrophil in the past, but isn't sure of the exact date and state "I think it was in January of 2005". This would be recorded with an occuranceDateRange of "January 2005" and an uncertainOccuranceDateCode of "estimated".
bridg:PerformedMedicalConditionResult.occurrenceDateRangeValidationCode
urn:HCTv1.0:CDE_2795658:Lab_Results.If_necessary__please_validate_the_neutrophil_recovery_date_response.
bridg:PerformedMedicalConditionResult.severityCode
severityCode
bridg:PerformedMedicalConditionResult.severityCode
false
bridg:PerformedMedicalConditionResult.severityCode
A coded value specifying the intensity of the condition.
bridg:PerformedMedicalConditionResult.severityCode
Moderate could be used to describe acne.
bridg:PerformedMedicalConditionResult.severityCode
Values of: none
bridg:PerformedMedicalConditionResult.severityCode
mild or trivial
bridg:PerformedMedicalConditionResult.severityCode
moderate or severe
bridg:PerformedMedicalConditionResult.severityCode
valve replacement
bridg:PerformedMedicalConditionResult.severityCode
unknown could be used for a aorta valvular insufficiency
bridg:PerformedMedicalConditionResult.severityCode
Derived from PerformedClinicalInterpretation.value(ANY=>CD) WHERE PerformedClinicalInterpretation > PerformedObservation [severity assessment] > DefinedObservation.nameCode = "assess severity" AND PerformedObservation [severity assessment] > AssessedResultRelationship > PerformedMedicalConditionResult
bridg:PerformedMedicalConditionResult.severityCode
urn:HCTv1.0:CDE_3021198:Diagnosis.Specify_the_severity_of_the_valvular_insufficiency:
bridg:PerformedNotification.message
message
bridg:PerformedNotification.message
false
bridg:PerformedNotification.message
The actual text that was included in the notification.
bridg:PerformedNotification.message
urn:C3PRv2.9:ScheduledNotification.message
bridg:PerformedNotification.message
urn:caAERSv2.2:NotificationBodyContent.content
bridg:PerformedNotification.messageTitle
messageTitle
bridg:PerformedNotification.messageTitle
false
bridg:PerformedNotification.messageTitle
The subject of the notification.
bridg:PerformedNotification.messageTitle
urn:C3PRv2.9:ScheduledNotification.title
bridg:PerformedObservation.approachAnatomicSiteCode
approachAnatomicSiteCode
bridg:PerformedObservation.approachAnatomicSiteCode
false
bridg:PerformedObservation.approachAnatomicSiteCode
A coded value specifying the anatomic location or access point for an observation.
bridg:PerformedObservation.approachAnatomicSiteCode
Anus for a colonoscopy observation
bridg:PerformedObservation.approachAnatomicSiteCode
Neither target anatomic site nor approach anatomic site is necessarily required or relevant for certain observations, however if either or both are present then the distinction between them is that the approach site is the acces point for the measurement or observation and the target site is what is ultimately being evaluated.
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:PerformedObservation.approachAnatomicSiteCode
urn:CDASHv1.1:VS.VSLOC
bridg:PerformedObservation.approachAnatomicSiteCode
urn:CTRv1.0:PerformedObservation.approachAnatomicSiteCode
bridg:PerformedObservation.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:VS.VSLOC
bridg:PerformedObservation.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:EG.EGLOC
bridg:PerformedObservation.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:FA.FALOC
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
approachAnatomicSiteLateralityCode
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
false
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is an access point for a observation.
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
bilateral
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
left
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
right
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
urn:CDASHv1.1:VS.VSLOC
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
urn:CTRv1.0:PerformedObservation.approachAnatomicSiteLateralityCode
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.2:FA.FALOC
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.2:VS.VSLOC
bridg:PerformedObservation.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.2:EG.EGLOC
bridg:PerformedObservation.bodyPositionCode
bodyPositionCode
bridg:PerformedObservation.bodyPositionCode
false
bridg:PerformedObservation.bodyPositionCode
A coded value specifying the 3-dimensional spatial orientation of a subject during a particular observation.
bridg:PerformedObservation.bodyPositionCode
supine
bridg:PerformedObservation.bodyPositionCode
trendelenburg
bridg:PerformedObservation.bodyPositionCode
standing
bridg:PerformedObservation.bodyPositionCode
urn:CDASHv1.1:EG.EGPOS
bridg:PerformedObservation.bodyPositionCode
urn:CDASHv1.1:VS.VSPOS
bridg:PerformedObservation.bodyPositionCode
urn:CTOM:ClinicalResult.bodyPositionCode
bridg:PerformedObservation.bodyPositionCode
urn:CTRv1.0:PerformedObservation.bodyPositionCode
bridg:PerformedObservation.bodyPositionCode
urn:SDTM_IGv3.1.1:VS.VSPOS
bridg:PerformedObservation.bodyPositionCode
urn:SDTM_IGv3.1.1:EG.EGPOS
bridg:PerformedObservation.bodyPositionCode
urn:SDTM_IGv3.1.2:EG.EGPOS
bridg:PerformedObservation.bodyPositionCode
urn:SDTM_IGv3.1.2:VS.VSPOS
bridg:PerformedObservation.bodySystemCode
bodySystemCode
bridg:PerformedObservation.bodySystemCode
false
bridg:PerformedObservation.bodySystemCode
A coded value specifying the anatomical structure that consists of organs and organ subclasses responsible for certain body functions.
bridg:PerformedObservation.bodySystemCode
gastrointestinal system
bridg:PerformedObservation.bodySystemCode
urinary system
bridg:PerformedObservation.bodySystemCode
hematopoietic system
bridg:PerformedObservation.bodySystemCode
urn:CTRv1.0:PerformedObservationResult.bodySystemCode
bridg:PerformedObservation.bodySystemCode
urn:NCI_CRF_Standard:CDE_3192540v1.0:_Medical_History_Review_of_Systems_Criteria_Category
bridg:PerformedObservation.bodySystemCode
urn:NCI_CRF_Standard:CDE_2182671v1.0:_Other_Body_System/Site_Text
bridg:PerformedObservation.bodySystemCode
urn:NCI_CRF_Standard:CDE_3192450v1.0:_Physical_Examination_Criteria_Category
bridg:PerformedObservation.bodySystemCode
urn:SDTM_IGv3.1.1:PE.PEBODSYS
bridg:PerformedObservation.bodySystemCode
urn:SDTM_IGv3.1.2:PE.PEBODSYS
bridg:PerformedObservation.focalDateRange
focalDateRange
bridg:PerformedObservation.focalDateRange
true
bridg:PerformedObservation.focalDateRange
The time period in which the observation result is held to be true.
bridg:PerformedObservation.focalDateRange
Derived from DefinedObservation.focalDateRange alone (i.e., directly from simple date ranges like 1990-1999) or from evaluating the expression in DefinedObservation.focalDateRange (which references a date that is now known).
bridg:PerformedObservation.focalDateRange
urn:CTOM:Diagnosis.confirmationDate
bridg:PerformedObservation.focalDateRange
urn:CTOM:DiseaseResponse.progressionDate
bridg:PerformedObservation.focalDateRange
urn:CTRv1.0:PerformedObservation.focalDateRange
in IndividualCaseSafetyReport
bridg:PerformedObservation.focalDateRange
urn:ICSRr2:CausalityAssessment.effectiveTime
bridg:PerformedObservation.focalDateRange
urn:NCI_CRF_Standard:CDE_2744943v1.0:_Adverse_Event_Begin_Assessment_Date
bridg:PerformedObservation.focalDateRange
urn:NCI_CRF_Standard:CDE_2006851v4.0:_Adverse_Event_Final_Assessment_Date
bridg:PerformedObservation.focalDateRange
urn:SDTM_IGv3.1.2:PC.PCEVLINT
bridg:PerformedObservation.focalDuration
focalDuration
bridg:PerformedObservation.focalDuration
true
bridg:PerformedObservation.focalDuration
The quantity of time in which the observation result is held to be true.
bridg:PerformedObservation.focalDuration
2 months is the focalDuration for a question such as "Have you smoked in the last 2 months?".
bridg:PerformedObservation.focalDuration
Derived from PerformedObservation.focalDateRange.
bridg:PerformedObservation.focalDuration
urn:CTOM:DiseaseResponse.progressionPeriodUnitOfMeasureCode
bridg:PerformedObservation.focalDuration
urn:CTOM:DiseaseResponse.progressionPeriod
bridg:PerformedObservation.focalDuration
urn:CTRv1.0:PerformedObservation.focalDuration
bridg:PerformedObservation.focalDuration
urn:SDTM_IGv3.1.1:QS.QSEVLINT
bridg:PerformedObservation.methodCode
methodCode
bridg:PerformedObservation.methodCode
false
bridg:PerformedObservation.methodCode
A coded value specifying the technique used to perform the observation.
bridg:PerformedObservation.methodCode
Arterial puncture
bridg:PerformedObservation.methodCode
sphygmomanometry (for blood pressure measurement)
bridg:PerformedObservation.methodCode
Global introspection
bridg:PerformedObservation.methodCode
algorithm
bridg:PerformedObservation.methodCode
bayesian (for Adverse Event causality)
bridg:PerformedObservation.methodCode
Estrogen Receptor Assay
bridg:PerformedObservation.methodCode
Progesterone Receptor Assay
bridg:PerformedObservation.methodCode
p53 Assay (for clinical result assay)
bridg:PerformedObservation.methodCode
urn:AE:PerformedProductInvestigation.evaluationMethodCode
bridg:PerformedObservation.methodCode
urn:AE:CausalAssessment.methodCode
bridg:PerformedObservation.methodCode
urn:CDASHv1.1:EG.EGMETHOD
bridg:PerformedObservation.methodCode
urn:CTOM:ClinicalResult.meansVitalStatusObtainedCode
bridg:PerformedObservation.methodCode
urn:CTOM:ClinicalResult.assayMethodCode
bridg:PerformedObservation.methodCode
urn:CTOM:ClinicalResult.labTechniqueCode
bridg:PerformedObservation.methodCode
urn:CTOM:LesionDescription.methodCode
bridg:PerformedObservation.methodCode
urn:CTRPv3.8:PerformedObservation.methodCode
bridg:PerformedObservation.methodCode
urn:CTRv1.0:PerformedObservation.methodCode
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3057363:Lab_Results.Specify_the_method_used_to_assess_left_ventricle_performance:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2974160:Lab_Results.Specify_other_paroxysmal_nocturnal_hemoglobinuria_test:
SLE biopsy type?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2749589:Involvement_and_Extent_of_Disease.What_was_the_systemic_lupus_erythematosus
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3179410:Lab_Results.Second_fungal_infection_confirmed_laboratory_procedure_name:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2760530:Specimen_Characteristics.Which_method_of_testing_cell_viability_was_used?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3009669:Lab_Results.Specify_the_index_used_to_report_the_value:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2767307:Techniques.Specify_the_other_tumor_cells_detection_method
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2861233:Procedures.What_method_was_used_to_assess_the_disease?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2963400:Lab_Results.What_type_of_neoplastic_cell_detection_method_was_performed?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3057325:Procedures.What_clinical_assessment_test_tool_was_used_to_determine_mental_development:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3179414:Lab_Results.Third_fungal_infection_confirmed_laboratory_procedure_name:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3179398:Lab_Results.First_fungal_infection_confirmed_laboratory_procedure_name:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2861466:Procedures.What_type_of_cytogenetic_analysis_was_the_disease_assessed_by?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2630451:Procedures.Specify_test_and_method_for_test_performed_on_other_infectious_disease_marker:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2775544:Techniques.What_tumor_cell_detection_method_was_used_?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2985297:Lab_Results.Specify_the_chimerism_laboratory_procedure_method_type:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3020053:Procedures.Specify_other_mental_process_development_testing_clinical_assessment_tool:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2778231:Techniques.Specify_other_tumor_cell_detection_method_used_prior_to_HCST
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2780165:Lab_Results.Chimerism_study_method_type:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2974158:Lab_Results.What_paroxysmal_nocturnal_hemoglobinuria_test_was_used?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_3031335:Procedures.Specify_disease_or_disorder_assessment_method:
s were used to evaluate the status?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2974019:Procedures.Which_method
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2978298:Tumor_Measurements.What_was_the_primary_neoplasm_size_assessment_method?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2749395:Involvement_and_Extent_of_Disease.What_was_the_systemic_sclerosis_biopsy_type?
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2785787:Specimen_Characteristics.Specify_cell_specimen_viable_laboratory_procedure:
bridg:PerformedObservation.methodCode
urn:HCTv1.0:CDE_2778929:Techniques.What_kind_of_method_was_used_to_detect_tumor_cells_after_purging?
in IndividualCaseSafetyReport
bridg:PerformedObservation.methodCode
urn:ICSRr2:CausalityAssessment.methodCode
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:CE.CEPRESP
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:EG.EGMETHOD
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:MB.MBMETHOD
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:MH.MHPRESP
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:PE.PEMETHOD
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:CM.CMPRESP
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:LB.LBMETHOD
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:MS.MSMETHOD
bridg:PerformedObservation.methodCode
urn:SDTM_IGv3.1.2:PC.PCMETHOD
bridg:PerformedObservation.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:PerformedObservation.targetAnatomicSiteCode
false
bridg:PerformedObservation.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of the observation.
bridg:PerformedObservation.targetAnatomicSiteCode
Lower intestine for a colonoscopy observation
bridg:PerformedObservation.targetAnatomicSiteCode
The target site of the result may be different than the target site of the activity (PerformedObservation) that generated it. For example, a chest x-ray (observation) has the target site of chest while the result might show an infiltration in the left lower lobe of the lung (target site of result), or a dermatological exam may check the skin across the whole body (target site of observation) while the result might identify a rash on the right leg (target site of result).
Neither target anatomic site nor approach anatomic site is necessarily required or relevant for certain observations, however if either or both are present then the distinction between them is that the approach site is where the measurement or observation is performed and the target site is what is ultimately being evaluated. The target site is often implicit in the definition of the observation itself.
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions
bridg:PerformedObservation.targetAnatomicSiteCode
urn:CTOM:Imaging.anatomicSiteCode
bridg:PerformedObservation.targetAnatomicSiteCode
urn:CTOM:Imaging.anatomicSiteCodeSystem
bridg:PerformedObservation.targetAnatomicSiteCode
urn:CTRPv3.8:PerformedObservation.targetSiteCode
bridg:PerformedObservation.targetAnatomicSiteCode
urn:CTRv1.0:PerformedObservation.targetAnatomicSiteCode
bridg:PerformedObservation.targetAnatomicSiteCode
urn:SDTM_IGv3.1.2:PE.PELOC
bridg:PerformedObservation.targetAnatomicSiteCode
urn:SDTM_IGv3.1.2:FA.FALOC
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
false
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for an observation.
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
bilateral
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
left
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
right
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:PerformedObservation.targetAnatomicSiteLateralityCode
urn:CTRv1.0:PerformedObservation.targetAnatomicSiteLateralityCode
bridg:PerformedObservationResult.baselineIndicator
baselineIndicator
bridg:PerformedObservationResult.baselineIndicator
false
bridg:PerformedObservationResult.baselineIndicator
Specifies whether the result is a starting point to which other results may be compared.
bridg:PerformedObservationResult.baselineIndicator
urn:CTRv1.0:PerformedObservationResult.baselineIndicator
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:QS.QSBLFL
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:MS.MSBLFL
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:LB.LBBLFL
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:FA.FABLFL
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:VS.VSBLFL
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:EG.EGBLFL
bridg:PerformedObservationResult.baselineIndicator
urn:SDTM_IGv3.1.2:MB.MBBLFL
bridg:PerformedObservationResult.baselineIndicator
urn:caAERSv2.2:AdverseEventReportingPeriod.isBaseline
bridg:PerformedObservationResult.comment
comment
bridg:PerformedObservationResult.comment
false
bridg:PerformedObservationResult.comment
Additional description of the observation result.
bridg:PerformedObservationResult.comment
Comments from the investigator regarding the condition of the specimen or any other observation.
bridg:PerformedObservationResult.comment
Comments in addition to the specimen condition from the central or performing laboratory describing the specimen.
bridg:PerformedObservationResult.comment
urn:CTOM:HistopathologyGrade.commentText
bridg:PerformedObservationResult.comment
urn:CTOM:DiseaseResponse.commentText
bridg:PerformedObservationResult.comment
urn:CTRv1.0:PerformedObservationResult.comment
in R_Product
bridg:PerformedObservationResult.comment
urn:ICSRr2:Characteristics.text
bridg:PerformedObservationResult.comment
urn:Lab:LabResult.referenceRangeComments
bridg:PerformedObservationResult.comment
urn:NCI_CRF_Standard:CDE_797v5.0:_Research_Comments_Text
bridg:PerformedObservationResult.comment
urn:SDTM_IGv3.1.1:CO.COVAL
bridg:PerformedObservationResult.comment
urn:SDTM_IGv3.1.2:CO.COVAL
bridg:PerformedObservationResult.comment
urn:caAERSv2.2:ReportReviewComment
bridg:PerformedObservationResult.comment
urn:caAERSv2.2:AdverseEvent.comments
bridg:PerformedObservationResult.comment
urn:caAERSv2.2:ReportingPeriodReviewComment
bridg:PerformedObservationResult.confidentialityCode
confidentialityCode
bridg:PerformedObservationResult.confidentialityCode
false
bridg:PerformedObservationResult.confidentialityCode
A coded value specifying the degree of privacy applicable for the observation result.
bridg:PerformedObservationResult.confidentialityCode
Do not reveal to study sponsor.
bridg:PerformedObservationResult.confidentialityCode
urn:CTOM:Observation.confidentialityCode
bridg:PerformedObservationResult.confidentialityCode
urn:CTOM:Histopathology.confidentialityCode
bridg:PerformedObservationResult.confidentialityCode
urn:CTOM:LesionDescription.confidentialityCode
bridg:PerformedObservationResult.confidentialityCode
urn:CTOM:ClinicalResult.confidentialityCode
bridg:PerformedObservationResult.confidentialityCode
urn:CTRv1.0:PerformedObservationResult.confidentialityCode
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.confidentialityCode
urn:ICSRr2:RelatedInvestigation.confidentialityCode
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.confidentialityCode
urn:ICSRr2:InvestigativeEvent.confidentialityCode
bridg:PerformedObservationResult.identifier
identifier
bridg:PerformedObservationResult.identifier
false
bridg:PerformedObservationResult.identifier
The unique symbol that establishes identity of the observation result.
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:EX.EXTRTCMP
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:EX.EXYN
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:EX.EXDOSADJ
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:CM.CMAENO
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:EG.EGREFID
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:CM.CMMHNO
bridg:PerformedObservationResult.identifier
urn:CDASHv1.1:SU.SUNCF
bridg:PerformedObservationResult.identifier
urn:CTOM:Imaging.imageIdentifier
bridg:PerformedObservationResult.identifier
urn:CTOM:Imaging.identifier
bridg:PerformedObservationResult.identifier
urn:CTRv1.0:PerformedObservationResult.identifier
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.identifier
urn:ICSRr2:ProductDefectAssessment.id
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.identifier
urn:ICSRr2:ObservationEvent.id
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.identifier
urn:ICSRr2:DefectReference.id
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.identifier
urn:ICSRr2:AdverseEventAssessment.id
bridg:PerformedObservationResult.identifier
urn:SDTM_IGv3.1.2:DV.DVREFID
bridg:PerformedObservationResult.identifier
urn:SDTM_IGv3.1.2:CE.CEREFID
bridg:PerformedObservationResult.identifier
urn:SDTM_IGv3.1.2:EG.EGREFID
bridg:PerformedObservationResult.identifier
urn:SDTM_IGv3.1.2:MH.MHREFID
bridg:PerformedObservationResult.reportedDate
reportedDate
bridg:PerformedObservationResult.reportedDate
false
bridg:PerformedObservationResult.reportedDate
The date (and time) on which the result is reported.
bridg:PerformedObservationResult.reportedDate
urn:AE:Reporter.initialReporterIndicator
bridg:PerformedObservationResult.reportedDate
urn:CDASHv1.1:MH.MHDAT
bridg:PerformedObservationResult.reportedDate
urn:CTOM:Histopathology.reportingDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:LesionEvaluation.evaluationDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:Observation.reportingDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:DiseaseResponse.evaluationDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:Diagnosis.evaluationDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:FemaleReproductiveCharacteristic.menopauseStartDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:QualitativeEvaluation.evaluationDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:Assessment.evaluationDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:ClinicalResult.reportingDate
bridg:PerformedObservationResult.reportedDate
urn:CTOM:LesionDescription.reportingDate
bridg:PerformedObservationResult.reportedDate
urn:CTRv1.0:PerformedObservationResult.reportedDate
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866525:Occurrences.Date_of_the_latest_cytogenetic_/_FISH_assessment:
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866139:Occurrences.What_date_was_the_relapse/progression_detected_by_a_clinical/hematological_method?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866135:Occurrences.What_date_was_the_relapse/progression_detected_by_a_cytogenetic/FISH_method?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866504:Occurrences.Date_of_current_clinical_/_hematologic_assessment_used_to_assess_the_disease_status
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866437:Occurrences.Date_the_cytogenetic_complete_remission_was_determined_via_FISH:
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2947021:Occurrences.Date_of_relapse:
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2951782:Diagnosis.What_was_the_date_of_the_PET_assessment?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2943067:Diagnosis.What_was_the_date_of_MDS_/_MPS_transformation?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2936575:Disease_Response.Specify_the_date_complete_remission_was_achieved:
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866462:Occurrences.Date_of_the_current_molecular_assessment_used_to_assess_the_disease_status.
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2944110:Occurrences.What_date_did_the_disease_relapse_or_progress?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2770410:Occurrences.What_is_the_documented_date_of_the_stable__mixed_chimerism?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2866133:Occurrences.What_date_was_the_relapse/progression_detected_by_a_molecular_method?
bridg:PerformedObservationResult.reportedDate
urn:HCTv1.0:CDE_2932795:Diagnosis.Date_of_diagnosis:
bridg:PerformedObservationResult.reportedDate
urn:NCI_CRF_Standard:CDE_2435009v1.1:_Protocol_Deviation_Notification_Date
bridg:PerformedObservationResult.reportedDate
urn:PSCv2.6:AdverseEvent.detectionDate
bridg:PerformedObservationResult.reportedDate
urn:SDTM_IGv3.1.1:MH.MHDTC
bridg:PerformedObservationResult.reportedDate
urn:SDTM_IGv3.1.2:MH.MHDTC
bridg:PerformedObservationResult.reportedDate
urn:caAERSv2.2:AdverseEventResponseDescription.statusDate
bridg:PerformedObservationResult.reportedDate
urn:caAERSv2.2:AdverseEvent.gradedDate
bridg:PerformedObservationResult.resultClassificationCode
resultClassificationCode
bridg:PerformedObservationResult.resultClassificationCode
false
bridg:PerformedObservationResult.resultClassificationCode
The highest level of the terminology describing the result distinguished by anatomical or physiological system, etiology, or purpose.
bridg:PerformedObservationResult.resultClassificationCode
Blood and lymphatic system disorders; Cardiac disorders; Congenital
bridg:PerformedObservationResult.resultClassificationCode
familial and genetic disorders; Ear and labyrinth disorders; Endocrine disorders; Eye disorders; Gastrointestinal disorders; General disorders and administration site conditions; Hepatobiliary disorders; Immune system disorders; Infections and infestations; Injury
bridg:PerformedObservationResult.resultClassificationCode
poisoning and procedural complications; Investigations; Metabolism and nutrition disorders; Musculoskeletal and connective tissue disorders; Neoplasms benign
bridg:PerformedObservationResult.resultClassificationCode
malignant and unspecified (incl cysts and polyps); Nervous system disorders; Pregnancy
bridg:PerformedObservationResult.resultClassificationCode
puerperium and perinatal conditions; Psychiatric disorders; Renal and urinary disorders; Reproductive system and breast disorders; Respiratory
bridg:PerformedObservationResult.resultClassificationCode
thoracic and mediastinal disorders; Skin and subcutaneous tissue disorders; Social circumstances; Surgical and medical procedures; Vascular disorders
bridg:PerformedObservationResult.resultClassificationCode
System Organ Class
bridg:PerformedObservationResult.resultClassificationCode
Note that the DSET data type means that more than one value can be specified for this attribute, however this is meant to be interpreted as more than one system, etiology or purpose, such as when a CRF has "check all that apply" instruction. This is not meant to imply that there would be more than one level of terminology or some sort of hierarchy of terms would be conveyed here.
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749891:Involvement_and_Extent_of_Disease.For_the_polymyositis-dermatomyositis__what_was_the_involved_organ_or_clinical_problem?
SLE, what was the involved organ or clinical problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749007:Involvement_and_Extent_of_Disease.For_the_systemic_lupus_erythematosus
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2685212:Involvement_and_Extent_of_Disease.Specify_the_other_involvement_of_the_systemic_sclerosis:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2750646:Involvement_and_Extent_of_Disease.Specify_the_type_of_wegener_granulomatosis_involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749969:Involvement_and_Extent_of_Disease.For_the_wegener_granulomatosis__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749929:Involvement_and_Extent_of_Disease.Specify_the_other_type_of_antiphospholipid_syndrome_involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749605:Involvement_and_Extent_of_Disease.For_the_sjogren_syndrome__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2674903:Involvement_and_Extent_of_Disease.Specify_the_other_involvement_for_sjogren_syndrome:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2797538:Involvement_and_Extent_of_Disease.Specify_the_type_of_organ_impairment_/disorder:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749918:Involvement_and_Extent_of_Disease.For_the_antiphospholipid_syndrome__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2750141:Involvement_and_Extent_of_Disease.For_the_rheumatoid_arthritis__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2686142:Involvement_and_Extent_of_Disease.For_the_psoriatic_arthritis_/_psoriasis_specify_the_other_involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2750535:Involvement_and_Extent_of_Disease.For_the_psoriatic_arthritis_/_psoriasis__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2750113:Involvement_and_Extent_of_Disease.For_the_polyarteritis_nodosa__classical_or_microscopic__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_3129555:Involvement_and_Extent_of_Disease.Was_there_extramedullary_and_/_or_extranodal_involvement?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749904:Involvement_and_Extent_of_Disease.Specify_the_type_of_polymyositis-dermatomyositis_involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2797573:Involvement_and_Extent_of_Disease.Specify_the_other_organ_impairment_/_disorder:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2953469:Involvement_and_Extent_of_Disease.Specify_the_lymphoma_organ_involved:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2748902:Involvement_and_Extent_of_Disease.For_the_systemic_sclerosis__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749910:Involvement_and_Extent_of_Disease.For_the_multiple_sclerosis__what_was_the_involved_organ_or_clinical_problem?
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2750529:Involvement_and_Extent_of_Disease.Specify_the_type_of_rheumatoid_arthritis_involvement:
SLE involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2749585:Involvement_and_Extent_of_Disease.Specify_the_type_of_systemic_lupus_erythematosus
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_3082350:Involvement_and_Extent_of_Disease.Specify_the_site_of_extranodal_involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2686158:Involvement_and_Extent_of_Disease.For_the_multiple_sclerosis__specify_the_other_involvement:
bridg:PerformedObservationResult.resultClassificationCode
urn:HCTv1.0:CDE_2750124:Involvement_and_Extent_of_Disease.Specify_the_type_of_polyarteritis_nodosa__classical_or_microscopic__involvement:
SOC
bridg:PerformedObservationResult.resultClassificationCode
urn:NCI_CRF_Standard:CDE_2943864v1.0:_MedDRA_System_Organ_Class
bridg:PerformedObservationResult.resultClassificationCode
urn:SDTM_IGv3.1.1:AE.AEBODSYS
bridg:PerformedObservationResult.resultClassificationCode
urn:SDTM_IGv3.1.1:MH.MHBODSYS
bridg:PerformedObservationResult.resultClassificationCode
urn:SDTM_IGv3.1.2:MH.MHBODSYS
bridg:PerformedObservationResult.resultClassificationCode
urn:SDTM_IGv3.1.2:CE.CEBODSYS
bridg:PerformedObservationResult.resultClassificationCode
urn:SDTM_IGv3.1.2:AE.AEBODSYS
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
false
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for an observation result.
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
bilateral
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
left
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
right
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:PerformedObservationResult.targetAnatomicSiteLateralityCode
urn:CTRv1.0:PerformedObservationResult.targetAnatomicSiteLateralityCode
bridg:PerformedObservationResult.typeCode
typeCode
bridg:PerformedObservationResult.typeCode
false
bridg:PerformedObservationResult.typeCode
A coded value specifying the kind of observation result.
bridg:PerformedObservationResult.typeCode
A single blood pressure observation has two results
bridg:PerformedObservationResult.typeCode
typeCode = "systolic" and typeCode = "diastolic".
bridg:PerformedObservationResult.typeCode
urn:CTOM:ClinicalResult.value
bridg:PerformedObservationResult.typeCode
urn:CTRPv3.8:ObservationResult.typeCode
bridg:PerformedObservationResult.typeCode
urn:CTRv1.0:PerformedObservationResult.typeCode
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.typeCode
urn:ICSRr2:AdverseEventAssessment.code
in R_Product
bridg:PerformedObservationResult.typeCode
urn:ICSRr2:Characteristics.code
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.typeCode
urn:ICSRr2:InvestigationCharacteristic.code
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.typeCode
urn:ICSRr2:ObservationEvent.code
bridg:PerformedObservationResult.uncertaintyCode
uncertaintyCode
bridg:PerformedObservationResult.uncertaintyCode
false
bridg:PerformedObservationResult.uncertaintyCode
A coded value specifying whether and to what degree this evaluation or observation has been asserted to be in doubt in any way.
bridg:PerformedObservationResult.uncertaintyCode
A patient might have had a cholecystectomy procedure in the past
bridg:PerformedObservationResult.uncertaintyCode
but isn't sure what the outcome was.
bridg:PerformedObservationResult.uncertaintyCode
urn:CTOM:Histopathology.uncertaintyCode
bridg:PerformedObservationResult.uncertaintyCode
urn:CTOM:LesionDescription.uncertaintyCode
bridg:PerformedObservationResult.uncertaintyCode
urn:CTOM:ClinicalResult.uncertaintyCode
bridg:PerformedObservationResult.uncertaintyCode
urn:CTOM:Observation.uncertaintyCode
bridg:PerformedObservationResult.uncertaintyCode
urn:CTRv1.0:PerformedObservationResult.uncertaintyCode
NAT for human immunodeficiency virus(HIV-1 performed; specify results
bridg:PerformedObservationResult.uncertaintyCode
urn:HCTv1.0:CDE_2695060:Lab_Results.If_FDA_licensed_nucleic_acid_amplification_test
bridg:PerformedObservationResult.value
value
bridg:PerformedObservationResult.value
false
bridg:PerformedObservationResult.value
Data or information that is determined by an act of observation.
bridg:PerformedObservationResult.value
The result of a lab test
bridg:PerformedObservationResult.value
physical finding
bridg:PerformedObservationResult.value
self-reported symptom.
bridg:PerformedObservationResult.value
The adverse event term code.
bridg:PerformedObservationResult.value
urn:AE:InvestigativeSubject.gestationPeriod
bridg:PerformedObservationResult.value
urn:AE:Assessment.textInterpretation
bridg:PerformedObservationResult.value
urn:AE:ProductObservation.value
bridg:PerformedObservationResult.value
urn:AE:Assessment.codedInterpretation
bridg:PerformedObservationResult.value
urn:AE:ProductInvestigation.evaluationResultCode
bridg:PerformedObservationResult.value
urn:AE:Animal.overallStateOfHealthCode
bridg:PerformedObservationResult.value
urn:AE:Person.numberOfSiblings
bridg:PerformedObservationResult.value
urn:AE:AdverseEvent.reactionText
bridg:PerformedObservationResult.value
urn:AE:AdverseEvent.adverseEventTermCode
bridg:PerformedObservationResult.value
urn:C3PR:StratificationCriterionPermissbleAnswer.permissibleAnswer
bridg:PerformedObservationResult.value
urn:C3PRv2.9:AdverseEvent.verbatim
bridg:PerformedObservationResult.value
urn:C3PRv2.9:DiseaseHistory.otherPrimaryDiseaseCode
bridg:PerformedObservationResult.value
urn:C3PRv2.9:SubjectStratificationAnswer
bridg:PerformedObservationResult.value
urn:C3PRv2.9:SubjectEligibilityAnswer.answerText
bridg:PerformedObservationResult.value
urn:CDASHv1.1:EG.EGPERF
bridg:PerformedObservationResult.value
urn:CDASHv1.1:AE.AEOCCUR
bridg:PerformedObservationResult.value
urn:CDASHv1.1:VS.VSORRES
bridg:PerformedObservationResult.value
urn:CDASHv1.1:MH.MHCTRL
bridg:PerformedObservationResult.value
urn:CDASHv1.1:CM.CMYN
bridg:PerformedObservationResult.value
urn:CDASHv1.1:DV.DVTERM
bridg:PerformedObservationResult.value
urn:CDASHv1.1:MH.MHOCCUR
bridg:PerformedObservationResult.value
urn:CDASHv1.1:DS.DSDECOD
bridg:PerformedObservationResult.value
urn:CDASHv1.1:LB.LBORRES
bridg:PerformedObservationResult.value
urn:CDASHv1.1:AE.AETERM
bridg:PerformedObservationResult.value
urn:CDASHv1.1:MH.MHYN
bridg:PerformedObservationResult.value
urn:CDASHv1.1:SC.SCORRES
bridg:PerformedObservationResult.value
urn:CDASHv1.1:PE.PEPERF
bridg:PerformedObservationResult.value
urn:CDASHv1.1:DV.DVDECOD
bridg:PerformedObservationResult.value
urn:CDASHv1.1:LB.LBORRESU
bridg:PerformedObservationResult.value
urn:CDASHv1.1:PE.PEDESC
bridg:PerformedObservationResult.value
urn:CDASHv1.1:AE.AEOUT
bridg:PerformedObservationResult.value
urn:CDASHv1.1:PE.PERES
bridg:PerformedObservationResult.value
urn:CDASHv1.1:EG.EGORRES
bridg:PerformedObservationResult.value
urn:CDASHv1.1:DV.DVYN
bridg:PerformedObservationResult.value
urn:CDASHv1.1:SC.SCPERF
bridg:PerformedObservationResult.value
urn:CDASHv1.1:DS.DSTERM
bridg:PerformedObservationResult.value
urn:CDASHv1.1:AE.AEYN
bridg:PerformedObservationResult.value
urn:CDASHv1.1:MH.MHTERM
bridg:PerformedObservationResult.value
urn:CDASHv1.1:CM.CMOCCUR
bridg:PerformedObservationResult.value
urn:CDASHv1.1:VS.VSORRESU
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.survivalStatusCode
bridg:PerformedObservationResult.value
urn:CTOM:DeathSummary.deathCauseText
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.performanceStatusCode
bridg:PerformedObservationResult.value
urn:CTOM:DiseaseResponse.courseDispositionCode
bridg:PerformedObservationResult.value
urn:CTOM:DiseaseResponse.responseCodeSystem
bridg:PerformedObservationResult.value
urn:CTOM:ParticipantEligibilityAnswer.answerText
bridg:PerformedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.stillBirthCount
bridg:PerformedObservationResult.value
urn:CTOM:DeathSummary.deathCauseCode
bridg:PerformedObservationResult.value
urn:CTOM:CancerStage.stageCodeSystem
bridg:PerformedObservationResult.value
urn:CTOM:Specimen.volume
bridg:PerformedObservationResult.value
urn:CTOM:Participant.employmentStatusCode
bridg:PerformedObservationResult.value
urn:CTOM:Diagnosis.diseaseDiagnosisCode
bridg:PerformedObservationResult.value
urn:CTOM:Neoplasm.cellTypeCode
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.painIndexCode
bridg:PerformedObservationResult.value
urn:CTOM:LesionEvaluation.evaluationCode
bridg:PerformedObservationResult.value
urn:CTOM:CancerStage.stageCode
bridg:PerformedObservationResult.value
urn:CTOM:AdverseEvent.outcomeCode
bridg:PerformedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.abortionIndicator
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.menstrualPatternTypeCode
bridg:PerformedObservationResult.value
urn:CTOM:ClinicalResult.value
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.performanceStatusCodeSystem
bridg:PerformedObservationResult.value
urn:CTOM:Histopathology.grossExamResultCode
bridg:PerformedObservationResult.value
urn:CTOM:ClinicalResult.valueUnitOfMeasureCode
bridg:PerformedObservationResult.value
urn:CTOM:Specimen.volumeUnitOfMeasureCode
bridg:PerformedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.menopauseAge
bridg:PerformedObservationResult.value
urn:CTOM:Participant.employmentStatusOtherText
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.menstrualIndicator
bridg:PerformedObservationResult.value
urn:CTOM:DiseaseResponse.responseCode
bridg:PerformedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.liveBirthCount
bridg:PerformedObservationResult.value
urn:CTOM:AdverseEvent.descriptionText
bridg:PerformedObservationResult.value
urn:CTOM:Participant.householdIncomeCode
bridg:PerformedObservationResult.value
urn:CTOM:FemaleReproductiveCharacteristic.firstLiveBirthAge
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.anamResultAccuracyPercent
bridg:PerformedObservationResult.value
urn:CTOM:Person.employmentStatusCode
bridg:PerformedObservationResult.value
urn:CTOM:Diagnosis.diseaseDiagnosisCodeSystem
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.survivalStatusDescriptionText
bridg:PerformedObservationResult.value
urn:CTOM:Person.householdIncomeCode
bridg:PerformedObservationResult.value
urn:CTOM:QualitativeEvaluation.painIndexCodeSystem
bridg:PerformedObservationResult.value
urn:CTRPv3.8:ObservationResult.resultCode
bridg:PerformedObservationResult.value
urn:CTRPv3.8:ObservationResult.resultText
bridg:PerformedObservationResult.value
urn:CTRPv3.8:ObservationResult.resultQuantity
bridg:PerformedObservationResult.value
urn:CTRPv3.8:ObservationResult.resultIndicator
bridg:PerformedObservationResult.value
urn:CTRv1.0:PerformedObservationResult.value
bridg:PerformedObservationResult.value
urn:CTRv1.0:PerformedObservationResult.categoryCode
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952877:Lab_Results.Urinary_monoclonal_light_chains:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769598:Adverse_Events.What_is_the_most_likely_cause_of_the_adverse_event?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2677067:Disease_Response.Specify_the_type_of_complete_remission_of_the_breast_cancer_at_the_time_of_transplantation:
SGOT?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2782608:Lab_Results.What_is_the_unit_of_measure_for_AST
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2969090:Lab_Results.What_is_the_value_of_vanillylmandelic_acid_measurement?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693547:Lab_Results.Second_B*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2756925:Lab_Results.What_is_the_unit_of_measure_for_the_Ig_test?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3117210:Lab_Results.Specify_the_testicular_cancer_stage:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2815530:Individuals.What_is_the_combined_househould_gross_annual_income?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2795420:Lab_Results.Did_the_recipient_recover_and_maintain_ANC_greater_than_or_equal_to_500/mmE3_following_the_decline?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2676557:Diagnosis.Was_the_breast_cancer_inflammatory_or_non-inflammatory?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952899:Lab_Results.What_is_the_unit_of_measure_for_serum_immunoglobulin_light_chain__Kappa?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760129:Lab_Results.Mononucleated_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760860:Diagnosis.What_is_the_liver_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2694901:Lab_Results.Second_DPB1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749839:Lab_Results.Were_tumor_cells_detected_in_collected_cells__before_purging_prior_to_HSCT?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073220:Lab_Results.What_is_the_reason_for_the_B_alleles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3009207:Disease__Disorder_or_Finding.Specify_the_hematologic_status:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2689272:Diagnosis.What_was_the_classification_of_the_immune_deficiency?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2770702:Biological_Process.Specify_the_etiology_of_the_other_organism:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2677074:Disease__Disorder_or_Finding.If_the_breast_cancer_was_in_the_state_of_relapse_at_the_time_of_transplantation__what_was_the_sensitivity_to_chemotherapy?
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2784431:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_2nd_organism_with_name
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2772026:Disease__Disorder_or_Finding.Specify_genetic_disease:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3028423:Lab_Results.Indicate_the_enzyme_that_was_evaluated_for_activity_level:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2691376:Lab_Results.For_the_polymyositis-dermatomyositis__were_the_EMG_results_typical_of_the_disease?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3010917:Diagnosis.What_is_the_type_of_Batten_disease?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704139:Lab_Results.First_DRB5_*_allele_designations:
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2784437:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_5th_organism_with_name
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2983177:Lab_Results.Specify_the_proliferative_index_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2964425:Diagnosis.Specify_the_histological_diagnosis_of_resected_tissue
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.CD19_
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3104029:Lab_Results.ER___cells_stained_positive:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3179295:Lab_Results.Does_the_recipient_have_clinical_significant_zygomycota_fungal_infection_history?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2689329:Lab_Results.For_systemic_lupus__erythematosus__what_was_the_total_complement_test_result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2771987:Lab_Results.Mesenchymal_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2816459:Behavior.What_is_the_average_number_of_packs_of_cigarettes_smoked_per_day?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2782511:Symptoms.Specify_the_symptoms_of_engraftment_syndrome:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2682913:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_test_results_at_diagnosis_for_the_other_antibody?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2875701:Physical_Description_of_Individuals.What_is_the_dosing_body_weight_unit_of_measure?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3179231:Lab_Results.Does_the_recipient_have_clinical_significant_rhizopus_fungal_infection_history?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780171:Lab_Results.Chimerism_study_cell_type:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685380:Diagnosis.Specify_the_other_type_of_leukemia:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2979356:Diagnosis.Specify_the_ratio_of_HER2_signals_to_17_centromere_signals:
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2784433:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_3rd_organism_with_name
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2969591:Involvement_and_Extent_of_Disease.What_was_the_stage_of_breast_cancer_at_diagnosis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693524:Lab_Results.First_A*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_64516//:Lab_Results.Provide_DNA_Index_of_Leukemic_Cells
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2738465:Disease__Disorder_or_Finding.What_was_the_cause_of_the_therapy-related_MDS/MPS?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2963549:Lab_Results.Did_hypercalcemia_occur?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2789977:Personal_attributes.Donor's_blood_type_and_Rh_factor:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2875642:Individuals.Weight
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965922:Lab_Results.What_is_the_IgE_level?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695256:Lab_Results.1st_A_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953022:Specimen_Characteristics.Specify_the_size_of_the_largest_neoplasm_mass:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2964752:Lab_Results.What_is_the_status_of_T-cell_engraftment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2991013:Lab_Results.What_is_the_unit_of_measure_for_leukocyte_enzyme_activity_level?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780721:Lab_Results.Chimerism_study_total_cells_examined:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950700:Lab_Results.Specify_the_lymphoma_histology:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798679:Property_or_Attribute.Have_you_smoked_cigarettes_within_the_past_year?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3061152:Lab_Results.What_is_the_percentage_of_hematocrit?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2801066:Diagnosis.Specify_the_diagnosis_of_liver_toxicity_by_the_type_of_clinical_signs__symptoms_or_evaluation:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953262:Individuals.Specify_the_type_of_health_insurance:
CFU were assessed, what was the total number of CFU-GM counted?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760382:Lab_Results.When_the_colony-forming_units
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2679802:Diagnosis.Specify_the_type_of_autoimmune_disease:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952925:Lab_Results.What_is_the_unit_of_measure_for_serum_immunoglobulin_light_chain_lambda?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953285:Affiliation_Type.Is_the_person_enrolled_in_school?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3136597:Biological_Process.What_was_the_sensitivity_of_the_disease_to_chemotherapy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760372:Lab_Results.Total_value_of_CD4+_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2951780:Lab_Results.Heavy_chain
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986435:Disease__Disorder_or_Finding.What_was_the_prognosis_type_of_seminoma?
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2784429:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_1st_organism_with_name
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2689280:Involvement_and_Extent_of_Disease.What_was_the_International_Staging_System_for_Myeloma_Stage?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967294:Anatomic_Sites.Number_of_tumors_present:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760303:Lab_Results.Total_value_of_CD3+_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769602:Adverse_Events.Specify_other_illness_cause_of_the_adverse_event:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2957553:Lab_Results.Specify_abnormality:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2181363:Diagnosis.Durie-Salmon_Stage
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704135:Lab_Results.DR51_specificity_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974120:Disease__Disorder_or_Finding.Specify_viral_hepatitis_type:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3179200:Lab_Results.Does_the_recipient_have_clinical_significant_aspergillus_fungal_infection_history?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986478:Disease__Disorder_or_Finding.Specify_testicular_non-seminomatous_germ_cell_tumor_prognosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3123936:Disease__Disorder_or_Finding.What_is_the_result_of_the_audiometric_test_assessed_at_the_speech_threshold_for_2000_hertz?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2180456:Lab_Results.Hepatitis_B_surface_antibody_Status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2860221:Lab_Results.Absolute_number_of_plasma_cells_in_blood_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Transgene__
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686163:Diagnosis.Specify_the_other_autoimmune_neurological_disorder:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2002710:Chronic_or_Associated_Diseases_and_Exposures.Specify_other
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3086802:Units_of_Measure.What_is_the_unit_of_measure_for_serum_IgG?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695284:Lab_Results.Second_B_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695323:Lab_Results.Second_DR_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3128032:Symptoms.What_were_the_chronic_lymphocytic_leukemia_symptoms?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704143:Lab_Results.Second_DRB5_*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2859803:Lab_Results.Plasma_cells_in_blood_percentage_value:
ies:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798745:Occurrences.Specify_the_other_malignancy
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950614:Lab_Results.What_was_the_status_of_the_serum_immunofixation_finding?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2679527:Diagnosis.Specify_the_type_of_other_solid_tumor:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2705046:Lab_Results.First_DRB3*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2963361:Lab_Results.Was_the_diagnositic_image_positive_for_CNS_tumor?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2691365:Lab_Results.For_the_polymyositis-dermatomyositis__were_the_biopsy_results_typical_of_the_disease?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2737648:Disease__Disorder_or_Finding.What_was_the_cause_of_the_therapy_related_AML?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2815190:Personal_attributes.What_is_the_person's_retirement_income_status?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2737638:Disease__Disorder_or_Finding.Specify_the_other_type_of_clinically_significant_comorbidity:
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2935457:Disease_Response.Specify_the_degree_of_disease_response_to_treatment
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2594609:Lab_Results.Was_the_lymphoma_or_lymphoproliferative_disease_EBV_positive?
Philadelphia chromosome+, Ph+, t(9;22(q34;q11, or variant OR bcr/abl+?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2688790:Diagnosis.What_was_the_classification_of_the_chronic_myelogenous_leukemia
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685158:Diagnosis.What_was_the_classification_of_the_histiocytic_disorder?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760804:Diagnosis.What_is_the_genitourinary_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.CD3_
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986133:Lab_Results.What_is_the_value_of_leukocyte_enzyme_activity_level?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685168:Diagnosis.What_was_the_classification_of_the_inherited_disorders_of_metabolism_/_osteopetrosis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2002838:Procedures.Total_number_of_axillary_lymph_nodes_examined
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2603692:Outcome_of_Therapy.What_was_the_maximum_Grade_of_acute_graft_versus_host_disease
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3009223:Disease__Disorder_or_Finding.Specify_the_renal_status:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2688882:Diagnosis.What_is_the_classification_of_the_other_leukemia?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3181117:Lab_Results.Specify_paroxysmal_nocturnal_hemoglobinuria_results:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3126069:Procedures.What_was_the_visual_eye_acuity_snellen_fraction_numerator?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760821:Diagnosis.What_is_the_hematologic_diagnostic_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2775874:Lab_Results.What_is_the_unit_of_measure_for_WBC?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2939877:Diagnosis.Specify_the_number_of_phases_experienced:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974122:Disease__Disorder_or_Finding.Specify_other_aplastic_anemia_etiology:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2815058:Personal_attributes.Is_the_person_an_adult_or_emancipated_minor?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2679800:Diagnosis.Specify_the_other_inherited_disorder_of_metabolism:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2795147:Lab_Results.What_is_the_percentage_of_neutrophils?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760451:Diagnosis.What_is_the_chromosome_abnormality_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798766:Lab_Results.What_is_the_LDH_lab_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3141318:Lab_Results.Specify_test_sensitivity_to_cross-linking_agents_test_results:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2729172:Lab_Results.What_was_the_unit_of_measure_for_the_total_volume_of_the_product_being_analyzed?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2677061:Disease__Disorder_or_Finding.If_the_breast_cancer_was_in_the_state_of_relapse_at_the_time_of_transplantation__what_was_the_number_of_the_relapse?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2675089:Diagnosis.What_was_the_W.H.O._classification_of_the_other_acute_leukemia?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2939337:Lab_Results.Specify_which_type_of_cytogenetic_and_or_molecular_abnormalities_showed_a_positive_result:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760281:Diagnosis.What_is_the_cardiovascular_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3212384:Lab_Results.Were_donor_cells_present_as_determined_by_non-quantitative_means?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3124170:Lab_Results.Did_any_cytogenetic_or_molecular_testing_for_BCR/ABL_or_Ph+_show_a_positive_result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3021261:Quality_of_Life.What_is_the_value_of_the_mental_process_development_assessment_score?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798645:Personal_attributes.What_is_the_blood_type_and_Rh_factor?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686194:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_C3_test_result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2911999:Diagnosis.What_was_the_classification_of_the_aplastic_anemia?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2939856:Disease__Disorder_or_Finding.How_many_blast_phases_occurred?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2977753:Lab_Results.Specify_the_histologic_findings_by_Shimada_classification:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685046:Disease_Response.If_there_was_a_relapse_of_hodgkin_lymphoma_at_the_time_of_transplantation__what_was_the_sensitivity_to_chemotherapy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769129:Involvement_and_Extent_of_Disease.Specify_contributing_cause_of_death:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965306:Disease__Disorder_or_Finding.What_is_the_cause_of_disease_type_?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3050012:Techniques.Specify_portion_of_cells_cryopreserved_prior_to_infusion
HBV surface antigen(HBsAg
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693568:Lab_Results.Test_results_of_infectious_disease_marker_for_hepatitis_B_virus
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2538920:Units_of_Measure.Height_Unit_of_Measure_UCUM_Code
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685390:Diagnosis.Specify_the_other_constitutional_anemia:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2895871:Disease__Disorder_or_Finding.What_type_of_the_cell_origin_of_the_new_malignancy_is_it?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760905:Diagnosis.Specify_the_other_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749826:Lab_Results.Were_tumor_cells_detected_in_circulating_blood_cells_prior_to_HSCT?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695304:Lab_Results.Number_of_DR_antigens_provided
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2962097:Disease__Disorder_or_Finding.Was_there_a_family_history_of_cancer_in_first_degree_relatives_under_40_years_of_age?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3030987:Lab_Results.What_is_the_value_of_serum_free_light_chains_lambda?
WNV using nucleic acid amplification test (NAT
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695096:Lab_Results.Test_results_of_infectious_disease_marker_for_west_nile_virus
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986573:Outcome_of_Therapy.Indicate_the_sensitivity_of_the_testicular_carcinoma_to_any_platinum-containing_chemotherapeutic_agent_administered:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760378:Specimen_Characteristics.Was_the_cell_viability_tested?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693560:Lab_Results.Second_C*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2705050:Lab_Results.Second_DRB3*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704223:Lab_Results.Second_DPA1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749870:Lab_Results.For_the_antiphospholipid_syndrome__what_was_the_result_of_the_laboratory_procedure?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2954716:Outcome_of_Therapy.Specify_the_sensitivity_of_myeloma_to_chemotherapy:
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Mesenchymal_cells
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695308:Lab_Results.First_DR_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2182896:Chronic_or_Associated_Diseases_and_Exposures.Have_you_smoked_at_least_100_cigarettes_in_your_entire_life?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2804619:Data_Source.Is_the_data_reported_on_this_form_based_on_contact_with_the_physician?
CSF total protein value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2866117:Lab_Results.Cerebrospinal_fluid
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769017:Involvement_and_Extent_of_Disease.Primary_cause_of_death:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760290:Lab_Results.CD34+_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Regulatory_T_cells
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2978596:Lab_Results.Specify_estrogen_receptor_assay_results:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693528:Lab_Results.Second_A*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2860225:Lab_Results.Absolute_number_of_plasma_cells_in_blood_unit_of_measure:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2180578:Disease__Disorder_or_Finding.Left_Ventricular_Ejection_Fraction_at_Rest
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749801:Lab_Results.Were_tumor_cells_detected_in_bone_marrow__in_the_interval_between_last_systemic_therapy_and_collection_prior_to_HSCT?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3031295:Lab_Results.What_is_the_value_of_urinary_monoclonal_light_chains?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Hematopoietic_stem_cells
antibodies to Human Immunodeficiency Viruses:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695078:Lab_Results.Test_results_of_infectious_disease_marker_for_Anti-HIV_1_and_anti-HIV_2
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2677079:Diagnosis.What_was_the_classification_of_the_other_malignancy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3061554:Lab_Results.Serum_beta-human_chorionic_gonadotropin_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704125:Lab_Results.Second_DRB4*_allele_designations:
NAT for hepatitis C virus performed; specify results
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695074:Procedures.Was_FDA_licensed_nucleic_acid_amplification_test
CR ever achieved in response to the HSCT?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2739683:Therapy_Results.Was_a_complete_remission
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986513:Outcome_of_Therapy.What_was_the_sensitivity_of_the_testicular_carcinoma_to_chemotherapy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2676358:Therapies.Did_graft_failure_occur?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685162:Diagnosis.Specify_the_other_histiocytic_disorder:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704098:Lab_Results.Bw4_specificity_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2514317:Diagnosis.CML_Lineage
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2802822:Lab_Results.What_is_the_unit_of_measure_for_the_cluster_of_differentiation?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073237:Lab_Results.What_is_the_reason_for_the_DPB1_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Transplant.Total_number_of_cells_infused
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749841:Lab_Results.For_the_systemic_sclerosis__what_was_the_laboratory_procedure_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2630453:Lab_Results.Specify_test_results_for_test_performed_on_other_infectious_disease_marker
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769114:Involvement_and_Extent_of_Disease.Contributing_cause_of_death:
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2784435:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_4th_organism_with_name
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2737130:Disease__Disorder_or_Finding.What_was_the_clinically_significant_co-existing_disease_or_organ_impairment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2434914:Eligibility.Menopausal_status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3188446:Diagnosis.Specify_the_enzyme_deficiency:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797508:Involvement_and_Extent_of_Disease.Specify_any_other_non-infectious_pulmonary_abnormalities_that_developed:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986315:Lab_Results.Specify_malignant_testicular_germ_cell_tumor_histology:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073228:Lab_Results.What_is_the_reason_for_the_DRB4_alleles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704262:Therapy_Doses.Was_the_entire_volume_of_product_infused?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2939332:Organ_Measurements.What_was_the_spleen_size?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760760:Diagnosis.What_is_the_gastrointestinal_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704184:Lab_Results.Second_DQA1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2815349:Disease__Disorder_or_Finding.How_many_prior_HSCTs_have_been_done?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2729902:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_results:
Anti-HTLV I / II:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695025:Lab_Results.Test_results_of_infectious_disease_marker_for_human_T-Lymphotropic_virus_antibody
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3008133:Disease__Disorder_or_Finding.Specify_the_cardiac_status:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861069:Lab_Results.What_is_the_unit_of_measure_for_serum_albumin?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2936204:Abnormal_Cell.Were_cytogenetic_abnormalities_present_at_diagnosis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760790:Diagnosis.Specify_the_other_gastrointestinal_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2692300:Diagnosis.Specify_the_other_juvenile_idiopathic_arthritis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2964762:Lab_Results.What_is_the_status_of_myeloid_engraftment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2871885:Procedures.What_is_the_cm_H2O_value_of_the_cerebrospinal_fluid_closing_pressure:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3086814:Lab_Results.What_is_the_oxygen_saturation_level_percentage?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749843:Lab_Results.For_the_systemic_sclerosis__what_was_the_result_of_the_laboratory_procedure?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797618:Outcome_of_Therapy.List_the_maximum_severity_of_acute_graft_versus_host_disease_skin_involvement:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695275:Lab_Results.First_B_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2676555:Involvement_and_Extent_of_Disease.What_was_the_stage_of_the_breast_cancer_at_diagnosis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2955919:Lab_Results.Specify_cell_line:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760306:Lab_Results.CD3+_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950698:Lab_Results.What_is_the_lymphoma_histology_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760374:Lab_Results.CD4+_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950619:Lab_Results.Specify_monoclonal_immunoglobulin_result:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760831:Diagnosis.Specify_the_other_hematologic_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685348:Diagnosis.Specify_the_other_type_of_plasma_cell_disorder:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760286:Lab_Results.Total_value_of_CD34+_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2771985:Lab_Results.Total_value_of_mesenchymal_cells:
CRID assignment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3158590:Medical_Records_and_Forms.What_is_the_indication_for_CIBMTR_recipient_ID
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2738971:Disease__Disorder_or_Finding.Specify_other_predisposing_condition:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953097:Lab_Results.Serum_Calcium_Unit_of_Measure
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693507:Lab_Results.Number_of_B_antigens_provided:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3103994:Biological_Process.What_was_the_sensitivity_of_the_lymphoma_to_chemotherapy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3128020:Disease__Disorder_or_Finding.What_was_the_chronic_lymphocytic_leukemia_histology_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2649435:Diagnosis.What_was_the_subtype_of_the_non-hodgkin_lymphoma_diffuse__large_B-cell_lymphoma?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967344:Individuals.Number_affected:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3128022:Diagnosis.Specify_other_autoimmune_disease:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2787461:Diagnosis.What_is_the_primary_disease_for_which_the_HSCT_was_performed?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953026:Lab_Results.What_is_the_serum_M_protein_unit_of_measure?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3024868:Disease__Disorder_or_Finding.Were_the_exam_results_normal_or_abnormal?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2785810:Involvement_and_Extent_of_Disease.What_was_the_maximum_extent_of_chronic_GVHD_during_this_period?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2936025:Lab_Results.Results_of_cytogenetic_testing:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974108:Lab_Results.What_was_the_gamma-enolase_value_?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2739534:Adverse_Events.What_type_of_Adverse_Events_were_associated_with_the_stem_cell_infusion?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2802820:Lab_Results.What_is_the_value_of_the_cluster_of_differentiation?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965920:Lab_Results.What_is_the_IgA_level?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2799091:Lab_Results.What_is_the_value_of_platelets?_0
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797534:Diagnosis.Specify_the_clinical_sign__symptom_or_evaluation_used_to_diagnose_liver_toxicity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798687:Chronic_or_Associated_Diseases_and_Exposures.How_many_years_did_the_recipient_smoke_cigarettes?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2729161:Lab_Results.Total_volume_of_product:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2729065:Adverse_Events.If_the_donor_died_as_a_result_of_the_collection__specify_the_cause_of_death:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2770355:Lab_Results.Was_the_disease_detected_by_molecular_analysis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3086799:Lab_Results.What_is_the_value_of_serum_IgG?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2951827:Diagnosis.What_was_the_result_of_the_PET_assessment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967232:Lab_Results.What_is_the_value_of_homovanillic_acid?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2756919:Lab_Results.What_is_the_value_of_the_immunoglobulin_test?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2773882:Lab_Results.CD8+_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695328:Lab_Results.Number_of_DQ_antigens_provided:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2748995:Techniques.Was_a_particular_tumor_cell_detection_method_used_after_purging?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3076040:Lab_Results.What_is_the_percentage_of_monocytes?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704199:Lab_Results.Number_of_DP_antigens_provided:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3181250:Lab_Results.Specify_drug_level:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2634620:Lab_Results.Hepatitis_A_antibody_status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686171:Diagnosis.Specify_the_other_autoimmune_cytopenia:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2675091:Diagnosis.Specify_the_type_of_other_acute_leukemia:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760808:Diagnosis.Specify_the_other_genitourinary_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2679790:Disease__Disorder_or_Finding.Specify_the_other_inherited_platelet_abnormalities:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3010717:Diagnosis.What_is_the_inheritance_of_immune_deficiency?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2494701:Pre-Preparative_Regimen.Which_scale_was_used_to_measure/report_the_functional_status?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073235:Lab_Results.What_is_the_reason_for_the_DQB1_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950911:Lab_Results.Is_the_histology_a_transformation_from_CLL?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974069:Involvement_and_Extent_of_Disease.What_is_the_Pediatric_Oncology_Group_Stage?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704246:Lab_Results.First_DP_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2694887:Lab_Results.First_DPB1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073243:Lab_Results.What_is_the_reason_for_the_DPA1_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760473:Diagnosis.Specify_the_chromosome_abnormality:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2005035:Lab_Results.Hemoglobin
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3118470:Medical_Records_and_Forms.Search_result:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2799093:Lab_Results.What_is_the_unit_of_measure_for_platelets?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2793799:Diagnosis.Diagnosis_of_chronic_GVHD_was_based_on:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2782552:Adverse_Events.Specify_the_other_hematopoietic_stem_cell_infusion_adverse_event_type
AML or acute nonlymphocytic leukemia (ANLL?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2682630:Diagnosis.What_was_the_W.H.O_classification_of_the_acute_myelogenous_leukemia
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2744521:Techniques.Specify_portion_manipulated:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2897746:Lab_Results.What_is_the_percent_of_basophils?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073233:Lab_Results.What_is_the_reason_for_the_DRB5_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965430:Symptoms.Did_chronic_diarrhea_occur_?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953272:Individuals.Specify_other_health_insurance:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686104:Diagnosis.Specify_the_other_hemoglobinopathy:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760540:Diagnosis.Specify_the_other_CNS_/_psychiatric_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760127:Lab_Results.Total_value_of_mononucleated_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2971688:Lab_Results.Specify_level_and_units:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695297:Lab_Results.Second_C_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2871881:Lab_Results.What_is_the_cm_H2O_value_of_the_cerebrospinal_fluid_opening_pressure:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2802770:Lab_Results.Specify_cluster_of_differentiation_type:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2558043:Disease_Response.What_was_the_recipient's_survival_status_at_latest_follow-up?
ALL:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2675085:Diagnosis.Specify_the_type_of_acute_lymphoblastic_leukemia
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2932807:Disease__Disorder_or_Finding.Specify_prior_disease:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952921:Lab_Results.What_is_the_value_of_serum_creatinine?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686200:Lab_Results.What_was_the_CPK_test_result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3020044:Disease__Disorder_or_Finding.What_is_the_central_nervous_system_abnormality_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861067:Lab_Results.Serum_albumin_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3123937:Lab_Results.What_is_the_eosinophils_percentage_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760898:Diagnosis.Specify_the_other_pulmonary_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974091:Involvement_and_Extent_of_Disease.Specify_the_Evans_Stage:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974113:Disease__Disorder_or_Finding.What_was_the_aplastic_anemia_etiology?
HIV-1 p24 antigen:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695029:Lab_Results.Test_results_of_infectious_disease_marker_for_human_immunodeficiency_virus
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686182:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_ANA_test_result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2003853:Pre-Preparative_Regimen.Performance_Status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2775872:Lab_Results.What_is_the_value_of_WBC:
kappa:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952892:Lab_Results.Serum_free_light_chains
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2785867:Activity.Was_the_cord_blood_unit_completely_frozen_when_it_arrived_at_your_center?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2985301:Lab_Results.Specify_the_chimerism_laboratory_procedure_cell_type:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3115777:Lab_Results.What_was_the_serum_alpha-fetoprotein_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780118:Lab_Results.What_is_the_value_of_hemoglobin?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760532:Diagnosis.What_is_the_CNS_/_psychiatric_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704175:Lab_Results.First_DQA1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2954522:Involvement_and_Extent_of_Disease.Specify_the_lymphoma_stage_of_organ_involvement:
lambda:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952923:Lab_Results.Serum_free_light_chains
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3158540:Therapies.Specify_other_indication_for_cellular_therapy:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693554:Lab_Results.First_C*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2795891:Outcome_of_Therapy.Overall_severity_of_chronic_GVHD:
m^2
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Recipient.Recipient_body_surface_area
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3017713:Molecular_Abnormality.What_was_the_outcome_of_the_cytogenetic_analysis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695347:Lab_Results.Second_DQ_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2793785:Quality_of_Life.What_was_the_Karnofsky_/_Lansky_score?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3179224:Lab_Results.Does_the_recipient_have_clinical_significant_zygomycosis_fungal_infection_history?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3028430:Lab_Results.What_is_the_value_of_the_enzyme_evaluated_for_activity_level?
e.g.,cord blood unit bag intact upon thawing?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2786671:Activity.Was_the_primary_container
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780726:Lab_Results.Chimerism_study_total_number_of_donor_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2964760:Lab_Results.What_is_the_status_of_B-cell_engraftment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3181148:Lab_Results.Specify_neutrophils_one_decimal_place_billion_per_liter_value:
HCV antibody (Anti-HCV
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695021:Lab_Results.Test_results_of_infectious_disease_marker_for_hepatitis_C_virus
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695343:Lab_Results.First_DQ_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3061542:Medical_Imaging.What_were_the_results_of_the_image_studies_performed?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967327:Individuals.Are_other_family_members_known_to_have_neuroblastoma_or_ganglioneuroma?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953024:Lab_Results.What_is_the_value_of_serum_monoclonal_M_protein?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2688923:Diagnosis.What_was_the_classification_of_plasma_cell_disorders?
STS
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695088:Lab_Results.Test_results_of_infectious_disease_marker_for_syphilis_using_serologic_testing_for_syphilis
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2968377:Individuals.What_was_the_other_genetic_disorder_in_the_first_degree_relative?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780733:Lab_Results.Chimerism_study_total_number_of_host_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2181361:Diagnosis.Durie-Salmon_Sub-stage
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704151:Lab_Results.DR52_specificity_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2738883:Disease__Disorder_or_Finding.Specify_predisposing_condition:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2860212:Lab_Results.What_was_the_status_of_the_monocyte_finding?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3028428:Lab_Results.Specify_the_other_disease_enzyme_evaluated_for_activity_level
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3126070:Procedures.What_was_the_visual_eye_acuity_snellen_fraction_denominator?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760660:Diagnosis.What_is_the_endocrine_disorder_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2689395:Diagnosis.Specify_the_other_vasculitis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3141228:Quality_of_Life.Lansky_Performance_Status_Score
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798756:Lab_Results.What_is_the_value_of_serum_glutamic_oxaloacetic_transferase?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2597018:Lab_Results.Lactate_Dehydrogenase
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2677117:Biological_Process.If_there_was_a_relapse_of_the_other_malignancy__what_was_the_sensitivity_to_chemotherapy?
ies occurred?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798697:Occurrences.Which_malignancy
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_58208_/:Diagnosis.Rai_Stage_Classification
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3105041:Disease-Disorder_Classification.What_was_the_classification_of_hematologic_disorder?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.CD8_
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2963407:Lab_Results.What_is_the_value_of_lymphocytes_present_in_bone_marrow?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2863881:Lab_Results.What_is_the_value_of_serum_ferritin?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798778:Lab_Results.What_is_the_unit_of_measure_for_LDH?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695291:Lab_Results.First_C_antigen_specificity
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2957357:UML_DEFAULT_CD.Progesterone_Receptor_status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3212372:Lab_Results.Were_host_cells_present_as_determined_by_non-quantitative_means?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965215:Chronic_or_Associated_Diseases_and_Exposures.Was_maternal_engraftment_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685061:Diagnosis.Specify_the_type_of_non-hodgkin_lymphoma:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704121:Lab_Results.First_DRB4*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861135:Lab_Results.What_was_the_percentage_of_plasma_cells_in_bone_marrow_from_the_unknown_source?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3017711:Molecular_Abnormality.Were_cytogenetics_tested?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686173:Diagnosis.Specify_the_other_autoimmune_bowel_disorder:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2968379:Individuals.Specify_other_genetic_disease:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3061213:Adverse_Events.What_is_the_percentage_of_body_surface_area_affected_by_skin_rash_due_to_engraftment_syndrome?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3158627:Therapies.What_is_the_indication_for_cellular_therapy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2970589:Lab_Results.Specify_copy_number:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3179207:Lab_Results.Does_the_recipient_have_clinical_significant_fusarium_fungal_infection_history?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2860890:Lab_Results.What_is_the_percentage_of_plasma_cells_in_bone_marrow_biopsy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685070:Diagnosis.Specify_the_other_T_/_NK_cell_lymphoma:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967342:Individuals.Specify_relationship:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2724626:Diagnosis.Primary_cancer_type
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2986313:Lab_Results.What_was_the_histology_type_of_the_malignant_testicular_germ_cell_tumor?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2970552:Lab_Results.Were_proto-oncogenes_detected?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798684:Property_or_Attribute.Have_you_smoked_cigarettes_prior_to_but_not_during_the_past_year?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2969621:Lab_Results.Was_the_biopsy_site_positive_for_neuroblastoma?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073224:Lab_Results.What_is_the_reason_for_the_DRB1_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073222:Lab_Results.What_is_the_reason_for_the_C_alleles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760275:Lab_Results.Nucleated_red_blood_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2782624:Lab_Results.What_is_the_value_of_total_serum_bilirubin?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950100:Disease__Disorder_or_Finding.What_kind_of_clinical_features_were_presented_?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2770662:Biological_Process.Specify_the_etiology_of_the_other_virus:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2969619:Eligibility.Specify_the_patient's_age_at_menopause:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760665:Diagnosis.Specify_the_other_endocrine_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073226:Lab_Results.What_is_the_reason_for_the_DRB3_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2940579:Diagnosis.Specify_which_accelerated_phase_symptoms_were_present:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2782626:Lab_Results.What_is_the_unit_of_measure_for_total_serum_bilirubin?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2772153:Lab_Results.Total_value_of_CD8+_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073239:Lab_Results.What_is_the_reason_for_the_DQA1_allelles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760071:Diagnosis.Specify_the_other_autoimmune_disease_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3021221:Diagnosis.Specify_the_valvular_insufficiency_type:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704108:Lab_Results.Bw6_specificity_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2932805:Disease__Disorder_or_Finding.What_was_the_prior_disease?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685385:Diagnosis.Specify_the_other_acquired_cytopenic_syndrome:
HBV core antibody (Anti HBc
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2694945:Lab_Results.Test_results_of_infectious_disease_marker_for_hepatitis_B_virus
CMV antibody (IgG or total:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695092:Lab_Results.Test_results_of_infectious_disease_marker_for_cytomegalovirus
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760894:Diagnosis.What_is_the_pulmonary_diagnosis_type?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.NK_cells
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2630200:Units_of_Measure.Weight_Unit_of_Measure_UCUM_Code
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2676535:Biological_Process.If_there_was_a_relapse_of_non-hodgkin_lymphoma_at_the_time_of_transplantation__what_was_the_sensitivity_to_chemotherapy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861046:Lab_Results.What_is_the_percent_of_blasts_in_blood?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2002839:Lab_Results.Number_of_positive_axillary_lymph_nodes
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3008193:Disease__Disorder_or_Finding.Specify_the_hepatic_status:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2681693:Pre-Preparative_Regimen.What_was_the_donor_test_results_for_the_presence_of_CMV-antibodies?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3123697:Disease__Disorder_or_Finding.What_were_the_results_for_the_tympanometry_assessment?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2180758:Disease__Disorder_or_Finding.Shortening_Fraction
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2969596:Diagnosis.Specify_breast_cancer_histology:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965903:Lab_Results.What_is_the_IgM_level?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2950916:Lab_Results.Immunochemical_Type
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686188:Lab_Results.For_the_systemic_lupus_erythematosus__what_was_the_ds_DNA_test_result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Fresh_product
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2873940:Diagnostic_or_Prognostic_Factor.Test_results_of_infectious_disease_marker_for_Epstein-Barr_antibody:
palifermin, Kepivance started or is there a plan to use it?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2681996:Therapies.Was_KGF
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2982953:Lab_Results.What_is_the_percentage_of_the_percent_of_cells_positive_for_neuroblastoma?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861060:Lab_Results.Serum_beta_2-microglobulin_unit_of_measure:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3204062:Individuals.What_adjusted_body_weight_was_used?
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.CD56_
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3031315:Lab_Results.What_is_the_unit_of_measure_for_urinary_monoclonal_light_chains?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760261:Lab_Results.Nucleated_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3057316:Lab_Results.What_is_the_value_of_the_cerebrospinal_fluid_total_protein_measurement?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2961440:Lab_Results.What_is_the_stroma-rich_histology?
s:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2784439:Lab_Results.For_the_bacterial_or_fungal_infection_cultures_performed_prior_to_infusion__specify_the_6th_organism_with_name
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3024910:Disease__Disorder_or_Finding.What_is_the_percentage_of_ejection_fraction?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2634596:Lab_Results.Hepatitis_B_-_DNA_status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2749876:Lab_Results.For_the_wegener_granulomatosis__what_was_the_result_of_the_laboratory_procedure?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3135354:Organ_Measurements.Specify_the_spleen_size_below_costal_margin_in_centimeters:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769651:Individuals.What_is_the_number_of_pregnancies?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965488:Lab_Results.What_is_the_mitogen_proliferation_response?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760234:Lab_Results.Total_value_of_nucleated_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3028432:Lab_Results.What_is_the_unit_of_measure_for_enzyme_evaluated_for_activity_level?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797722:Involvement_and_Extent_of_Disease.Specify_the_other_non-infectious_liver_toxicity:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2867504:Lab_Results.Serum_creatinine_2_decimal_place_value:
s of death:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2768641:Outcome_of_Therapy.Specify_the_other_HSCT_related_main_cause
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797645:Outcome_of_Therapy.List_the_maximum_severity_of_the_acute_graft_versus_host_disease_upper_intestinal_tract_involvement:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760294:Diagnosis.Specify_the_other_cardiovascular_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685066:Diagnosis.Specify_the_type_of_other_B-cell_lymphoma:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965492:Lab_Results.What_is_the_natural_killer_cell_function?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2679566:Disease__Disorder_or_Finding.What_was_the_classification_of_the_platelet_disorder?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2494565:Diagnosis.What_was_the_primary_disease_for_which_the_HSCT_was_performed?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2871879:Lab_Results.Was_the_cerebrospinal_fluid_opening_pressure_known?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965208:Lab_Results.What_is_the_percentage_of_lymphocytes?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2936194:Lab_Results.Specify_BCR/ABL_or_other_molecular_tests_results:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2939876:Disease__Disorder_or_Finding.Specify_the_number_of_blast_phases:
CRID assignment:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3158516:Medical_Records_and_Forms.Specify_other_indication_for_CIBMTR_recipient_ID
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952507:Lab_Results.Which_monoclonal_bands_were_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2771962:Lab_Results.Total_value_of_NK_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798800:Lab_Results.What_is_the_unit_of_measure_for_serum_creatinine?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2867502:Lab_Results.Serum_creatinine:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3129551:Involvement_and_Extent_of_Disease.What_was_the_Binet_stage?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3031376:Disease__Disorder_or_Finding.What_is_the_result_of_the_method_used_to_assess_disease?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797633:Outcome_of_Therapy.List_the_maximum_severity_of_the_acute_graft_versus_host_disease_lower_intestinal_tract_involvement:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965477:Lab_Results.What_is_the_status_of_B-cell_function?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695266:Lab_Results.2nd_A_antigen_specificity
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2952509:Lab_Results.Was_the_monoclonal_band_type_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693502:Lab_Results.Number_of_A_antigens_provided:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2962101:Disease__Disorder_or_Finding.Specify_the_family_history_of_cancer_in_first_degree_relatives_under_40_years_of_age:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704158:Lab_Results.DR53_specificity_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686055:DONOR'.For_an_HLA-mismatched_related_donor__what_was_the_degree_of_mismatch:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686147:Diagnosis.Specify_the_other_arthritis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686111:Diagnosis.Specify_the_other_SCID:
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Frozen_product
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2691374:Lab_Results.For_the_dermatomyositis__was_there_a_rash_present_that_was_typical_of_the_disease?
e.g., insulated shipping containers and unit cassette intact when they arrived at your center?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2785785:Activity.Were_the_secondary_containers
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2860911:Lab_Results.What_is_the_value_of_plasma_cells_in_bone_marrow_aspirate?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_58265_/:Lab_Results.Marrow_Cellularity_Status
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2658051:Lab_Results.Light_Chain_Involved
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Effector_T_cells
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2694875:Lab_Results.First_DQB1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2681619:Pre-Preparative_Regimen.What_was_the_recipient's_test_results_for_the_presence_of_CMV-antibodies?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2962099:Disease__Disorder_or_Finding.What_was_the_family_history_of_cancer_in_first_degree_relatives_under_40_years_of_age?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2971761:Lab_Results.Were_any_other_molecular_abnormalities_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3081978:Diagnosis.What_was_the_subtype_for_which_the_HSCT_was_performed?
after resection?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_62732//:Therapy_Results.Has_residual_primary_tumor_been_detected
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861058:Lab_Results.Serum_beta_2_microglobulin_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2982573:Lab_Results.What_was_the_result_of_the_bone_marrow_laboratory_procedure?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2861157:Lab_Results.What_is_the_percent_of_blasts_in_the_bone_marrow?
velafermin started or is there a plan to use it?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2682005:Therapies.As_part_of_a_toxicity_modifying_regimen__was_FGF
CML: Part 1 of 2.At the time of transplantation, what was the number of the status of the CML?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2682797:Chronic_Myelogenous_Leukemia
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2676483:Diagnosis.Specify_the_type_of_hodgkin_lymphoma:
CFU were assessed, what was the total number of colonies counted?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2730798:Lab_Results.When_the_colony-forming_units
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965899:Lab_Results.What_is_the_IgG_level?
NAT for human immunodeficiency virus(HIV-1 performed; specify results
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2695060:Lab_Results.If_FDA_licensed_nucleic_acid_amplification_test
SLE, what was the C4 test result?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2689324:Lab_Results.For_the_systemic_lupus_erythematosus
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780738:Lab_Results.Chimerism_study_percent_of_donor_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2963521:Lab_Results.Leukemia_cell_type:
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.CD4_
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693511:Lab_Results.Number_of_C_antigens_provided:
kg
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Recipient.Recipient_weight
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2954746:Therapies.At_what_point_in_the_disease_course_was_the_HSCT_performed?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974177:Diagnosis.What_was_the_primary_CNS_disease_for_which_the_HSCT_was_performed?
kappa:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3030985:Lab_Results.What_is_the_value_of_serum_free_light_chains
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2738448:Diagnosis.What_was_the_MDS_or_myeloproliferative_disease_classification?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760279:Lab_Results.Total_value_of_nucleated_red_blood_cells:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798928:Lab_Results.What_is_the_hemoglobin_lab_value?
%:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2935895:Molecular_Abnormality.Specify_the_Philadelphia_chromosome_positive_metaphases_value
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2775909:Lab_Results.What_is_the_unit_of_measure_for_hemoglobin?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2794427:Specimen_Characteristics.Percent_Cells_Viable:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2677072:Disease__Disorder_or_Finding.If_the_breast_cancer_was_in_the_state_of_relapse_at_the_time_of_transplantation__was_the_cancer_local_or_metastatic?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2780745:Lab_Results.Chimerism_study_percent_of_host_cells:
s diagnosed with neuroblastoma or ganglioneuroma:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967337:Individuals.Specify_the_family_member
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3181189:Lab_Results.Specify_reticulocytes_one_decimal_place_billion_per_liter_value:
histology:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2787346:Disease__Disorder_or_Finding.Specify_the_result_of_the_diagnosis_based_on_evidence_from_the_biopsy
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2646370:Lab_Results.PgR___cells_stained_positive
Chronic
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2681691:Chronic_or_Associated_Diseases_and_Exposures.What_was_the_recipient's_test_results_for_the_presence_of_CMV-antibodies?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2782521:Lab_Results.Was_the_disease_detected_by_cytogenetic_analysis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3057303:Quality_of_Life.What_was_the_Vineland_adaptive_behavior_scales_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967358:Individuals.Is_there_a_family_history_of_other_genetic_diseases_in_first-degree_blood_relatives?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693564:Lab_Results.First_DRB1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2626962:Procedures.Number_of_metaphases_examined
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2686127:Diagnosis.Specify_the_other_immune_deficiency:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2974055:Involvement_and_Extent_of_Disease.Specify_the_International_Neuroblastoma_Staging_System_disease_stage:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2771967:Lab_Results.NK_cells_exponent_value:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2798924:Lab_Results.What_is_the_lymphocytes_lab_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3123938:Disease__Disorder_or_Finding.What_is_the_result_of_the_audiometric_test_assessed_at_the_speech_threshold_for_500_hertz?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2962060:Involvement_and_Extent_of_Disease.What_was_the_extent_stage_of_the_CNS_tumor?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2760867:Diagnosis.Specify_the_other_liver_disease_diagnosis:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2946347:Involvement_and_Extent_of_Disease.What_kind_of_disease_present?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2953095:Lab_Results.What_is_the_value_of_serum_calcium?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2967346:Individuals.Number_unknown:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2980333:Involvement_and_Extent_of_Disease.Specify_the_recurrent_disease_present_in_another_site:
bridg:PerformedObservationResult.value
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.CAR_
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3128021:Disease__Disorder_or_Finding.Specify_the_Chronic_Lymphocytic_Leukemia_histology:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2962086:Involvement_and_Extent_of_Disease.What_was_the_history_of_co-existing_phakomatosis?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2963374:Lab_Results.Was_any_tumor_present_in_the_biopsy?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693543:Lab_Results.First_B*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2785801:Lab_Results.When_the_colony-forming_units_were_assessed__was_there_growth?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2965468:Lab_Results.What_is_the_status_of_T-cell_function?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2691627:Disease_Response.If_the_plasma_cell_disorder_was_treated__what_was_the_number_of_the_response?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3098936:Individuals.What_is_the_reason_for_the_missing_number_of_pregnancies?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2694882:Lab_Results.Second_DQB1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2954687:Symptoms.Specify_the_systemic_symptoms:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2693570:Lab_Results.Second_DRB1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2912001:Diagnosis.What_was_the_classification_of_the_congenital_abnormalities_of_erythrocyte_differentiation_or_function?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2769109:Involvement_and_Extent_of_Disease.Specify_primary_cause_of_death:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704210:Lab_Results.First_DPA1*_allele_designations:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2685309:Diagnosis.Specify_the_type_of_other_connective_tissue_disease:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2874163:Individuals.Height
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2793779:Diagnosis.What_was_the_type_of_chronic_GVHD_onset?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2728988:Adverse_Events.Specify_the_life-threatening_complications_that_the_donor_experienced_during_or_after_the_collection:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3073218:Lab_Results.What_is_the_reason_for_the_A_alleles_missing_value?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_3030931:Lab_Results.What_is_the_value_of_platelets?
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2797671:Outcome_of_Therapy.List_the_maximum_severity_of_acute_graft_versus_host_disease_liver_involvement:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2971763:Lab_Results.Specify_other_molecular_abnormality:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2866119:Lab_Results.What_is_the_unit_of_measure_for_the_cerebrospinal_fluid_total_protein:
bridg:PerformedObservationResult.value
urn:HCTv1.0:CDE_2704252:Lab_Results.Second_DP_antigen_specificity:
bridg:PerformedObservationResult.value
urn:HL7SP:VerificationEvent.value
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.value
urn:ICSRr2:AdverseEventAssessment.text
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.value
urn:ICSRr2:InvestigationCharacteristic.value
in IndividualCaseSafetyReport
bridg:PerformedObservationResult.value
urn:ICSRr2:ObservationEvent.value
in R_Product
bridg:PerformedObservationResult.value
urn:ICSRr2:Characteristics.value
bridg:PerformedObservationResult.value
urn:Lab:LabResult.textResult
bridg:PerformedObservationResult.value
urn:Lab:LabResult.numericPrecision
bridg:PerformedObservationResult.value
urn:Lab:LabResult.referenceTextList
bridg:PerformedObservationResult.value
urn:Lab:LabResult.numericResult
bridg:PerformedObservationResult.value
urn:Lab:LaboratoryResult.numericResult
bridg:PerformedObservationResult.value
urn:LabViewer2.2:LabResultUnitOfMeasure.code
bridg:PerformedObservationResult.value
urn:LabViewer2.2:LaboratoryResult.numericPrecision
bridg:PerformedObservationResult.value
urn:LabViewer2.2:LaboratoryResult.textResult
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2538246v1.0:_MedDRA_Adverse_Event_Code
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2201348v1.0:_Adverse_Event_Suspected_Other_Attribution_Text_Name
AJCC Edition 7 Pathologic Regional Lymph Node N Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419395v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_323v3.0:_Common_Toxicity_Criteria_Adverse_Event_Term_Type
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2787947v1.0:_Laboratory_Test_Result_Unit_of_Measure_Unified_Code_for_Units_of_Measure_Code
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2003874v3.0:_Medical_History_Description
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3133353v1.0:_Common_Terminology_Criterio_for_Adverse_Events_Version_4.0_Mapped_Low_Level_Term_MedDRA_Code
AJCC Edition 7 Clinical Regional Lymph Node N Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419389v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2179892v1.0:_Adverse_Event_Cancer_Treatment_Related_Type
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_58208v3.0:_CLL_Leukemia_RAI_Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2183360v2.0:_Laboratory_Test_Result_Numeric_Value
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2435038v1.0:_Protocol_Deviation_Description_Text
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2902396v1.0:_CML_Disease_Phase_Category
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3125302v1.1:_Common_Terminology_Criteria_for_Adverse_Events_Version_4.0_Low_Level_Term_Name
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2848650v1.0:_Binet_Staging_System_Stage
AJCC Edition 7 Pathologic Tumor T Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419393v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2902402v1.0:_Lymphoma_B-Symptoms_Medical_Record_Documented_Indicator
AJCC Edition 7 Pathologic Distant Metastasis M Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419406v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3192550v1.0:_Medical_History_Review_of_Systems_Finding_Type
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2689280v1.0:_Plasma_Cell_Myeloma_International_Staging_System_for_Myeloma_Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2201880v1.0:_Patient_Abnormal_Physical_Examination_Specify
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2902443v1.0:_Hodgkin's_Lymphoma_Modified_Ann_Arbor_Staging_System_Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2746517v1.0:_Adverse_Event_Outcome_Type
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2188132v1.0:_Adverse_Event_Verbatim_Term_Text
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3192455v1.0:_Physical_Examination_Finding_Type
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2902390v1.0:_Pediatric_Lymphoid_Cancer_St._Jude_Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3116943v1.0:_Gynecologic_Tumor_Grouping_FIGO_2009_Cervical_Carcinoma_Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2181363v1.0:_Myeloma_Diagnosis_Stage
AJCC Edition 7 Clinical Distant Metastasis M Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419391v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
AJCC Edition 7 Group Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419407v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2902417v1.0:_Lymphoma_Ann_Arbor_Staging_System_Stage
AJCC Edition 7 Clinical Tumor T Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3419387v1.0:_Breast_Cancer_American_Joint_Committee_on_Cancer
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2004106v3.0:_Dose_Limiting_Toxicity_Ind
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_2902378v1.0:_Prostate_Carcinoma_Whitmore-Jewett_System_Stage
bridg:PerformedObservationResult.value
urn:NCI_CRF_Standard:CDE_3241064v1.0:_Laboratory_Test_Result_Character_Value
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:IE.IESTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:IE.IEORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PESTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESCONG
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:CM.CMOCCUR
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESMIE
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:TS.TSVAL
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESLIFE
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AEDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AETERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:MH.MHOCCUR
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AEREL
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PEORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESCAN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:MH.MHDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PESTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PESTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGLOINC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:DV.DVDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSLOINC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:EG.EGORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:DS.DSTERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESDTH
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:PE.PEORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:SC.SCSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AEOUT
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:MH.MHTERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:LB.LBLOINC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:QS.QSSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AERELNST
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:VS.VSSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.1:AE.AESDISAB
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:FA.FASTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MS.MSORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:VS.VSSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:LB.LBORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MH.MHOCCUR
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MB.MBORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PP.PPORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MB.MBSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PE.PESTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:AE.AEDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:AE.AETERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PE.PEORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:QS.QSSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:EG.EGSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:QS.QSSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PP.PPSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PP.PPORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:VS.VSSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:VS.VSORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:SC.SCSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:SC.SCORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:EG.EGORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MB.MBRESCAT
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:SC.SCSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:QS.QSORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:FA.FASTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MS.MSORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:FA.FAORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MH.MHTERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:LB.LBORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:DV.DVTERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:AE.AEOUT
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MB.MBSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:EG.EGSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:FA.FAORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:FA.FASTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PC.PCORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PP.PPSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:SC.SCORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:LB.LBSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:IE.IESTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:VS.VSSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:SU.SUOCCUR
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:DS.DSTERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MB.MBORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MS.MSSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:DV.DVDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:CE.CETERM
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PE.PEORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:VS.VSORRES
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PC.PCORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MS.MSSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:FA.FAOBJ
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MS.MSSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:EG.EGFXN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:CM.CMOCCUR
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:SC.SCSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:EG.EGORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:QS.QSORRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MH.MHDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MB.MBSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PC.PCSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:CE.CEOCCUR
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:LB.LBSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:LB.LBSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:MS.MSRESCAT
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:DS.DSDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:CE.CEDECOD
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PC.PCSTRESN
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PC.PCSTRESC
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:EG.EGSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:PP.PPSTRESU
bridg:PerformedObservationResult.value
urn:SDTM_IGv3.1.2:QS.QSSTRESC
bridg:PerformedObservationResult.value
urn:caAERSv2.2:DiseaseHistory___AbstractStudyDisease
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.jartCode
bridg:PerformedObservationResult.value
urn:caAERSv2.2:CtcTerm.term___AdverseEventCtcTerm
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___AdverseEventMeddraLowLevelTerm
bridg:PerformedObservationResult.value
urn:caAERSv2.2:MeddraVersion.name___AdverseEventMeddraLowLevelTerm
bridg:PerformedObservationResult.value
urn:caAERSv2.2:PreExistingCondition.meddraLowLevelTerm___SAEReportPreExistingCondition
bridg:PerformedObservationResult.value
urn:caAERSv2.2:CtcTerm.ctepCode___AdverseEvent
bridg:PerformedObservationResult.value
urn:caAERSv2.2:CtcTerm.select___AdverseEventCtcTerm
bridg:PerformedObservationResult.value
urn:caAERSv2.2:SAEReportPreExistingCondition.other
bridg:PerformedObservationResult.value
urn:caAERSv2.2:Lab.units
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___AdverseEvent
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AdverseEventResponseDescription.presentStatus
bridg:PerformedObservationResult.value
urn:caAERSv2.2:PreExistingCondition.meddraLowLevelTerm___StudyParticipantPreExistingCondition
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AdverseEventResponseDescription.eventAbate
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.costartSymbol
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AdverseEventResponseDescription.causeOfDeath
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.version_id
bridg:PerformedObservationResult.value
urn:caAERSv2.2:PreExistingCondition.text___SAEReportPreExistingCondition
bridg:PerformedObservationResult.value
urn:caAERSv2.2:ParticipantHistory.height
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AdverseEvent___AbstractAdverseEventTerm
bridg:PerformedObservationResult.value
urn:caAERSv2.2:ParticipantHistory.weight
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AdverseEventResponseDescription.studyDrugInterrupted
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.icd9Code
bridg:PerformedObservationResult.value
urn:caAERSv2.2:LabValue.value
bridg:PerformedObservationResult.value
urn:caAERSv2.2:DiseaseHistory.otherPrimaryDisease
bridg:PerformedObservationResult.value
urn:caAERSv2.2:PreExistingCondition.meddraLowLevelTermCode___SAEReportPreExistingCondition
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.icd9CmCode
bridg:PerformedObservationResult.value
urn:caAERSv2.2:StudyParticipantPreExistingCondition.other
bridg:PerformedObservationResult.value
urn:caAERSv2.2:PreExistingCondition.text___StudyParticipantPreExistingCondition
bridg:PerformedObservationResult.value
urn:caAERSv2.2:Ctc.name___AdverseEventCtcTerm
bridg:PerformedObservationResult.value
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bridg:PerformedObservationResult.value
urn:caAERSv2.2:PreExistingCondition.meddraLowLevelTermCode___StudyParticipantPreExistingCondition
bridg:PerformedObservationResult.value
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bridg:PerformedObservationResult.value
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bridg:PerformedObservationResult.value
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bridg:PerformedObservationResult.value
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bridg:PerformedObservationResult.value
urn:caAERSv2.2:StudyParticipantAssignment.baselinePerformance
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.hartsCode
bridg:PerformedObservationResult.value
urn:caAERSv2.2:AbstractMeddraDomain.icd10Code
bridg:PerformedObservationResult.value
urn:caAERSv2.2:StudyParticipantDiseaseHistory.otherPrimaryDisease
bridg:PerformedObservationResult.valueCodeModifiedText
valueCodeModifiedText
bridg:PerformedObservationResult.valueCodeModifiedText
false
bridg:PerformedObservationResult.valueCodeModifiedText
A character string that is a revision of the original text observation result to enable the coding of the text.
bridg:PerformedObservationResult.valueCodeModifiedText
If the originalText is "hedache"
bridg:PerformedObservationResult.valueCodeModifiedText
the valueCodeModifiedText could be changed to "headache"
bridg:PerformedObservationResult.valueCodeModifiedText
so that the text can be successfully coded.
bridg:PerformedObservationResult.valueCodeModifiedText
In the context of BRIDG, text modification occurs a single time for a given instance of originalText.
bridg:PerformedObservationResult.valueCodeModifiedText
urn:CTRPv3.8:ObservationResult.resultCodeModifiedText
bridg:PerformedObservationResult.valueCodeModifiedText
urn:CTRv1.0:PerformedObservationResult.valueCodeModifiedText
bridg:PerformedObservationResult.valueCodeModifiedText
urn:SDTM_IGv3.1.1:AE.AEMODIFY
bridg:PerformedObservationResult.valueCodeModifiedText
urn:SDTM_IGv3.1.1:PE.PEMODIFY
bridg:PerformedObservationResult.valueCodeModifiedText
urn:SDTM_IGv3.1.1:MH.MHMODIFY
bridg:PerformedObservationResult.valueCodeModifiedText
urn:SDTM_IGv3.1.2:MH.MHMODIFY
bridg:PerformedObservationResult.valueCodeModifiedText
urn:SDTM_IGv3.1.2:PE.PEMODIFY
bridg:PerformedObservationResult.valueCodeModifiedText
urn:SDTM_IGv3.1.2:AE.AEMODIFY
bridg:PerformedObservationResult.valueNullFlavorReason
valueNullFlavorReason
bridg:PerformedObservationResult.valueNullFlavorReason
false
bridg:PerformedObservationResult.valueNullFlavorReason
The text and/or code that describes why no result was provided.
bridg:PerformedObservationResult.valueNullFlavorReason
Subject refused to answer question.
bridg:PerformedObservationResult.valueNullFlavorReason
Error message returned by equipment to explain why the device was unable to produce a result.
bridg:PerformedObservationResult.valueNullFlavorReason
This value should only be populated if PerformedObservationResult.value is null.
bridg:PerformedObservationResult.valueNullFlavorReason
urn:BRIDGSCC:Model_Integrity
bridg:PerformedObservationResult.valueNullFlavorReason
urn:CTRv1.0:PerformedObservationResult.valueNullFlavorReason
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3030971:Lab_Results.What_was_the_reason_for_the_laboratory_procedure_specimen_source_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2771977:Lab_Results.What_is_the_reason_for_the_NK_cells_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2974126:Disease__Disorder_or_Finding.What_is_the_reason_for_the_viral_hepatitis_type_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2775889:Lab_Results.What_is_the_reason_for_the_lymphocytes_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3057314:Data_Source.If_necessary__specify_the_reason_for_the_missing_visual_acuity_value:
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3181147:Lab_Results.What_is_the_reason_for_the_drug_level_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2978413:Tumor_Measurements.What_is_the_reason_for_the_primary_neoplasm_size_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2799095:Lab_Results.What_is_the_reason_for_the_platelets_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2953093:Lab_Results.What_was_the_status_of_the_serum_calcium_finding?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3085846:Quality_of_Life.What_is_the_Vineland_Adaptive_Behavior_Scales_performance_type?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2730853:Lab_Results.When_the_colony-forming_units_were_assessed__was_the_total_number_of_colonies_unknown?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2775883:Lab_Results.What_is_the_reason_for_the_neutrophils_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3024912:Data_Source.What_is_the_reason_for_the_ejection_fraction_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2773885:Lab_Results.Did_laboratory_procedure_test_for_CD8+cells?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2816461:Behavior.What_is_the_reason_for_the_cigarette_average_daily_pack_use_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2974128:Disease__Disorder_or_Finding.What_is_the_reason_for_the_aplastic_anemia_etiology_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2798802:Lab_Results.What_is_the_reason_for_the_serum_creatinine_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3024914:Data_Source.What_is_the_reason_for_the_shortening_fraction_result_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3020350:Quality_of_Life.What_is_the_reason_for_the_mental_process_development_assessment_score_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3024947:Quality_of_Life.What_is_the_mental_development_testing_score_type?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2775876:Lab_Results.What_is_the_reason_for_the_WBC_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2798689:Chronic_or_Associated_Diseases_and_Exposures.What_is_the_reason_for_the_smoking_duration_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3057305:Quality_of_Life.What_is_the_reason_for_the_Vineland_adaptive_behavior_scales_score_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2775911:Lab_Results.What_is_the_reason_for_the_hemoglobin_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2782618:Lab_Results.What_is_the_reason_for_the_Serum_Glutamic_Oxaloacetic_Transferase_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2756923:Lab_Results.What_is_the_reason_for_the_immunoglobulin_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2780740:Lab_Results.What_is_the_reason_for_the_chimerism_study_percent_of_donor_cells_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2775920:Lab_Results.What_is_the_reason_for_the_hematocrit_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2802830:Lab_Results.What_is_the_reason_for_the_cluster_of_differentiation_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2771989:Lab_Results.What_is_the_reason_for_the_mesenchymal_cells_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2760398:Lab_Results.When_the_colony-forming_units_were_assessed__was_the_total_number_of_CFU-GM_unknown?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2782628:Lab_Results.What_is_the_reason_for_the_total_serum_bilirubin_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2798786:Lab_Results.What_is_the_reason_for_the_lactate_dehydrogenase_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2965152:Disease_Response.What_was_the_reason_the_best_response_to_disease_not_assessed?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_2780747:Lab_Results.What_is_the_reason_for_the_chimerism_study_percent_of_host_cells_missing_value?
bridg:PerformedObservationResult.valueNullFlavorReason
urn:HCTv1.0:CDE_3024908:Lab_Results.What_is_the_reason_for_the_oxygen_saturation_percentage_level_missing_value?
bridg:PerformedProcedure.approachAnatomicSiteCode
approachAnatomicSiteCode
bridg:PerformedProcedure.approachAnatomicSiteCode
false
bridg:PerformedProcedure.approachAnatomicSiteCode
A coded value specifying the anatomic location or access point for a procedure.
bridg:PerformedProcedure.approachAnatomicSiteCode
Arm for an injection
bridg:PerformedProcedure.approachAnatomicSiteCode
trans-abdominal for a nephrectomy.
bridg:PerformedProcedure.approachAnatomicSiteCode
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:AE:Intervention.approachSite
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:CDASHv1.1:EX.EXLOC
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:CTRv1.0:PerformedProcedure.approachAnatomicSiteCode
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:HCTv1.0:CDE_2769666:Anatomic_Sites.What_is_the_anatomic_site_of_the_central_venous_access_catheter?
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:HCTv1.0:CDE_2769668:Anatomic_Sites.Specify_the_other_site_of_the_central_line_placement:
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:HCTv1.0:CDE_2416537:Therapy_Doses.Radiation_Field
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:PerformedProcedure.approachAnatomicSiteCode
urn:SDTM_IGv3.1.2:EX.EXLOC
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
approachAnatomicSiteLateralityCode
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
false
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is an access point for a procedure.
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
bilateral
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
left
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
right
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:CDASHv1.1:EX.EXLOC
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:CTRv1.0:PerformedProcedure.approachAnatomicSiteLateralityCode
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:PerformedProcedure.approachAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.2:EX.EXLOC
bridg:PerformedProcedure.methodCode
methodCode
bridg:PerformedProcedure.methodCode
false
bridg:PerformedProcedure.methodCode
A coded value specifying the technique that is used to perform the procedure.
bridg:PerformedProcedure.methodCode
Finger stick
bridg:PerformedProcedure.methodCode
veni puncture
bridg:PerformedProcedure.methodCode
Abdominal/ ascites effusion
bridg:PerformedProcedure.methodCode
Biopsy
bridg:PerformedProcedure.methodCode
Bronchial alveolar lavage (BAL) (for specimen collection)
bridg:PerformedProcedure.methodCode
Open
bridg:PerformedProcedure.methodCode
laparoscopic (for cholecystectomy)
bridg:PerformedProcedure.methodCode
urn:CTOM:SpecimenAcquisition.methodCode
bridg:PerformedProcedure.methodCode
urn:CTRv1.0:PerformedProcedure.methodCode
bridg:PerformedProcedure.methodCode
urn:HCTv1.0:CDE_2748813:Therapies.Specify_the_other_malignant_cell_removal_method:
bridg:PerformedProcedure.methodCode
urn:HCTv1.0:CDE_2789998:Tissue_Banking.What_method_was_used_to_thaw_the_product?
bridg:PerformedProcedure.methodCode
urn:HCTv1.0:CDE_2790003:Tissue_Banking.Specify_other_thaw_method:
bridg:PerformedProcedure.methodCode
urn:Lab:SpecimenCollection.method
bridg:PerformedProcedure.methodCode
urn:LabViewer2.2:SpecimenCollection.type
bridg:PerformedProcedure.methodCode
urn:LabViewer2.2:SpecimenCollection.method
bridg:PerformedProcedure.methodCode
urn:SDTM_IGv3.1.1:EG.EGMETHOD
bridg:PerformedProcedure.methodCode
urn:SDTM_IGv3.1.1:LB.LBMETHOD
bridg:PerformedProcedure.methodCode
urn:caAERSv2.2:RadiationIntervention.administration
bridg:PerformedProcedure.nonReasonCode
nonReasonCode
bridg:PerformedProcedure.nonReasonCode
false
bridg:PerformedProcedure.nonReasonCode
A coded value specifying the motivation, cause or rationale that is explicitly NOT why an activity occurred.
bridg:PerformedProcedure.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:PerformedProcedure.targetAnatomicSiteCode
false
bridg:PerformedProcedure.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of a procedure.
bridg:PerformedProcedure.targetAnatomicSiteCode
Kidney (or a nephrectomy)
bridg:PerformedProcedure.targetAnatomicSiteCode
Multiple contiguous sites within the same organ system may be referenced.
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:AE:Intervention.targetSite
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:Procedure.anatomicSiteCodeSystem
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:Surgery.anatomicSiteCode
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:SpecimenAcquisition.anatomicSiteCodeSystem
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:Radiation.anatomicSiteCode
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:Surgery.anatomicSiteCodeSystem
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:Radiation.anatomicSiteCodeSystem
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:SpecimenAcquisition.anatomicSiteCode
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTOM:Procedure.anatomicSiteCode
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:CTRv1.0:PerformedProcedure.targetAnatomicSiteCode
s
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:HCTv1.0:CDE_2954787:Therapies.Specify_other_surgery_site
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:HCTv1.0:CDE_64160//:Anatomic_Sites.Site_of_Biopsy
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:HCTv1.0:CDE_2957282:Therapies.What_is_the_site_of_radiation_therapy?
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:HCTv1.0:CDE_2952974:Therapies.What_was_the_radiation_field?
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:HCTv1.0:CDE_2980936:Anatomic_Sites.Specify_the_other_site_of_orthopedic_surgery
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:HCTv1.0:CDE_2980893:Anatomic_Sites.Site_of_orthopedic_surgery
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:SDTM_IGv3.1.2:MB.MBLOC
bridg:PerformedProcedure.targetAnatomicSiteCode
urn:caAERSv2.2:Lab.site
bridg:PerformedProcedure.targetAnatomicSiteConditionCode
targetAnatomicSiteConditionCode
bridg:PerformedProcedure.targetAnatomicSiteConditionCode
false
bridg:PerformedProcedure.targetAnatomicSiteConditionCode
A coded value specifying the state of the target anatomic site.
bridg:PerformedProcedure.targetAnatomicSiteConditionCode
The subject's left arm was bruised where the IV was inserted.
bridg:PerformedProcedure.targetAnatomicSiteConditionCode
urn:CTOM:SpecimenAcquisition.siteConditionCode
bridg:PerformedProcedure.targetAnatomicSiteConditionCode
urn:CTRv1.0:PerformedProcedure.targetAnatomicSiteConditionCode
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
false
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for a procedure.
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
bilateral
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
left
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
right
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
urn:CTRv1.0:PerformedProcedure.targetAnatomicSiteLateralityCode
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:PerformedProcedure.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.2:MB.MBLOC
bridg:PerformedProductInvestigationResult.conclusion
conclusion
bridg:PerformedProductInvestigationResult.conclusion
false
bridg:PerformedProductInvestigationResult.conclusion
A text or otherwise formatted description of the final results drawn from the investigation.
bridg:PerformedProductInvestigationResult.conclusion
urn:AE:ProductInvestigation.conclusionsText
bridg:PerformedProductInvestigationResult.conclusion
urn:CTRv1.0:PerformedProductInvestigationResult.conclusion
in IndividualCaseSafetyReport
bridg:PerformedProductInvestigationResult.conclusion
urn:ICSRr2:ProductDefectAssessment.text
bridg:PerformedProductInvestigationResult.defectTypeCode
defectTypeCode
bridg:PerformedProductInvestigationResult.defectTypeCode
false
bridg:PerformedProductInvestigationResult.defectTypeCode
A coded value specifying the kind of device-related events that characterize the reported event/problem.
bridg:PerformedProductInvestigationResult.defectTypeCode
malfunction
bridg:PerformedProductInvestigationResult.defectTypeCode
urn:AE:ProductInvestigation.defectType
bridg:PerformedProductInvestigationResult.defectTypeCode
urn:CTRv1.0:PerformedProductInvestigationResult.defectTypeCode
bridg:PerformedProductInvestigationResult.deviceMalfunctionCode
deviceMalfunctionCode
bridg:PerformedProductInvestigationResult.deviceMalfunctionCode
false
bridg:PerformedProductInvestigationResult.deviceMalfunctionCode
A coded value specifying the defect or malfunction that occurred during use of the suspect device whether or not the problem is associated with an adverse event.
bridg:PerformedProductInvestigationResult.deviceMalfunctionCode
Codes are FDA CDRH device codes.
bridg:PerformedProductInvestigationResult.deviceMalfunctionCode
urn:AE:ProductInvestigation.deviceMalfunctionCode
bridg:PerformedProductInvestigationResult.deviceMalfunctionCode
urn:CTRv1.0:PerformedProductInvestigationResult.deviceMalfunctionCode
bridg:PerformedProductInvestigationResult.evaluationConclusionCode
evaluationConclusionCode
bridg:PerformedProductInvestigationResult.evaluationConclusionCode
false
bridg:PerformedProductInvestigationResult.evaluationConclusionCode
A coded value specifying the relevant fact within the context of the evaluation final results for a reported suspect medical device.
bridg:PerformedProductInvestigationResult.evaluationConclusionCode
Based on FDA CDRH Conclusion Codes.
bridg:PerformedProductInvestigationResult.evaluationConclusionCode
urn:AE:ProductInvestigation.evaluationConclusionCode
bridg:PerformedProductInvestigationResult.evaluationConclusionCode
urn:CTRv1.0:PerformedProductInvestigationResult.evaluationConclusionCode
bridg:PerformedProductTransport.methodCode
methodCode
bridg:PerformedProductTransport.methodCode
false
bridg:PerformedProductTransport.methodCode
A coded value specifying the technique that is used to transport the product.
bridg:PerformedProductTransport.methodCode
frozen gel pack
bridg:PerformedProductTransport.methodCode
room temperature per transplant center request
bridg:PerformedProductTransport.methodCode
urn:HCTv1.0:CDE_2785777:Activity.Specify_shipping_environment:
s:
bridg:PerformedProductTransport.methodCode
urn:HCTv1.0:CDE_2785775:Activity.Specify_the_shipping_environment_of_the_product
bridg:PerformedProductTransport.standardTimeIndicator
standardTimeIndicator
bridg:PerformedProductTransport.standardTimeIndicator
false
bridg:PerformedProductTransport.standardTimeIndicator
Specifies whether the time of the product transport is specified using standard (as opposed to daylight savings) time.
bridg:PerformedProductTransport.standardTimeIndicator
If the location and date are known, this data is derivable.
bridg:PerformedProductTransport.standardTimeIndicator
urn:HCTv1.0:CDE_2774729:Therapies.Is_time_of_receipt_of_product_standard_time_or_daylight_savings_time?
bridg:PerformedProtocolDeviation.categoryCode
categoryCode
bridg:PerformedProtocolDeviation.categoryCode
false
bridg:PerformedProtocolDeviation.categoryCode
A coded value specifying a classification of protocol deviation.
bridg:PerformedProtocolDeviation.categoryCode
Concomitant Medications
bridg:PerformedProtocolDeviation.categoryCode
Data Integrity Compromised
bridg:PerformedProtocolDeviation.categoryCode
Eligibility not checked
bridg:PerformedProtocolDeviation.categoryCode
Eligibility waiver
bridg:PerformedProtocolDeviation.categoryCode
Informed Consent
bridg:PerformedProtocolDeviation.categoryCode
Other specify
bridg:PerformedProtocolDeviation.categoryCode
Study Procedures
bridg:PerformedProtocolDeviation.categoryCode
Treatment [NCI CRF Standard examples]
bridg:PerformedProtocolDeviation.categoryCode
urn:CTRv1.0:PerformedProtocolDeviation.categoryCode
bridg:PerformedProtocolDeviation.categoryCode
urn:NCI_CRF_Standard:CDE_2740412v1.0:_Protocol_Deviation_Category
bridg:PerformedProtocolDeviation.categoryCode
urn:NCI_CRF_Standard:CDE_2740419v1.0:_Protocol_Deviation_Other_Category_Descriptive_Text
bridg:PerformedProtocolDeviation.categoryCode
urn:SDTM_IGv3.1.1:DV.DVCAT
bridg:PerformedProtocolDeviation.categoryCode
urn:SDTM_IGv3.1.2:DV.DVCAT
bridg:PerformedProtocolDeviation.occurrenceDateRange
occurrenceDateRange
bridg:PerformedProtocolDeviation.occurrenceDateRange
false
bridg:PerformedProtocolDeviation.occurrenceDateRange
The date and time span specifying when the protocol deviation began and ended.
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:CDASHv1.1:DV.DVENDAT
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:CDASHv1.1:DV.DVSTTIM
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:CDASHv1.1:DV.DVSTDAT
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:CDASHv1.1:DV.DVENTIM
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:CTRv1.0:PerformedProtocolDeviation.occurrenceDateRange
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:NCI_CRF_Standard:CDE_2434998v1.0:_Protocol_Deviation_Occurrence_Date
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:SDTM_IGv3.1.1:DV.DVENDTC
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:SDTM_IGv3.1.1:DV.DVSTDTC
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:SDTM_IGv3.1.2:DV.DVSTDTC
bridg:PerformedProtocolDeviation.occurrenceDateRange
urn:SDTM_IGv3.1.2:DV.DVENDTC
bridg:PerformedProtocolDeviation.severityCode
severityCode
bridg:PerformedProtocolDeviation.severityCode
false
bridg:PerformedProtocolDeviation.severityCode
A coded value specifying the intensity of a protocol deviation.
bridg:PerformedProtocolDeviation.severityCode
major
bridg:PerformedProtocolDeviation.severityCode
moderate
bridg:PerformedProtocolDeviation.severityCode
minor
bridg:PerformedProtocolDeviation.severityCode
urn:NCI_CRF_Standard:CDE_2740401v1.0:_Protocol_Deviation_Severity_Type
bridg:PerformedProtocolDeviation.subcategoryCode
subcategoryCode
bridg:PerformedProtocolDeviation.subcategoryCode
false
bridg:PerformedProtocolDeviation.subcategoryCode
A coded value specifying a subdivision within a larger category of a protocol deviation.
bridg:PerformedProtocolDeviation.subcategoryCode
urn:CTRv1.0:PerformedProtocolDeviation.subcategoryCode
bridg:PerformedProtocolDeviation.subcategoryCode
urn:SDTM_IGv3.1.2:DV.DVSCAT
bridg:PerformedStudyAgentTransfer.originalQuantity
originalQuantity
bridg:PerformedStudyAgentTransfer.originalQuantity
true
bridg:PerformedStudyAgentTransfer.originalQuantity
The amount and unit of study agent transferred in original units.
bridg:PerformedStudyAgentTransfer.originalQuantity
Original units can be derived from the translation attribute of the PQ data type PerformedStudyAgentTransfer.quantity.
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:CDASHv1.1:DA.DAORRES
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:CDASHv1.1:DA.DAORRESU
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:CTRv1.0:PerformedStudyAgentTransfer.originalQuantity
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:SDTM_IGv3.1.1:DA.DAORRES
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:SDTM_IGv3.1.1:DA.DAORRESU
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:SDTM_IGv3.1.2:DA.DAORRES
bridg:PerformedStudyAgentTransfer.originalQuantity
urn:SDTM_IGv3.1.2:DA.DAORRESU
bridg:PerformedStudyAgentTransfer.quantity
quantity
bridg:PerformedStudyAgentTransfer.quantity
false
bridg:PerformedStudyAgentTransfer.quantity
The amount and unit of study agent transferred in standard or canonical units.
bridg:PerformedStudyAgentTransfer.quantity
urn:CTRv1.0:PerformedStudyAgentTransfer.quantity
bridg:PerformedStudyAgentTransfer.quantity
urn:SDTM_IGv3.1.1:DA.DAORRES
bridg:PerformedStudyAgentTransfer.quantity
urn:SDTM_IGv3.1.1:DA.DAORRESU
bridg:PerformedStudyAgentTransfer.quantity
urn:SDTM_IGv3.1.1:DA.DASTRESC
bridg:PerformedStudyAgentTransfer.quantity
urn:SDTM_IGv3.1.2:DA.DASTRESN
bridg:PerformedStudyAgentTransfer.quantity
urn:SDTM_IGv3.1.2:DA.DASTRESU
bridg:PerformedStudySubjectMilestone.informedConsentDate
informedConsentDate
bridg:PerformedStudySubjectMilestone.informedConsentDate
true
bridg:PerformedStudySubjectMilestone.informedConsentDate
The date (and time) the study subject gives official consent by signing the official consent form.
bridg:PerformedStudySubjectMilestone.informedConsentDate
Derived from PerformedStudySubjectMilestone.dateRange WHERE PerformedActivity > DefinedActivity.nameCode = "obtain informed consent".
bridg:PerformedStudySubjectMilestone.informedConsentDate
urn:C3PR:StudySubject.informedConsentSignedDate
bridg:PerformedStudySubjectMilestone.informedConsentDate
urn:CTOM:StudyParticipantAssignment.informedConsentFormSignedDate
bridg:PerformedStudySubjectMilestone.informedConsentDate
urn:CTRPv3.8:PerformedSubjectMilestone.informedConsentDate
bridg:PerformedStudySubjectMilestone.informedConsentDate
urn:CTRv1.0:PerformedStudySubjectMilestone.informedConsentDate
bridg:PerformedStudySubjectMilestone.informedConsentDate
urn:LabViewer2.2:SubjectAssignment.informedConsentFormSignedDate
bridg:PerformedStudySubjectMilestone.informedConsentIndicator
informedConsentIndicator
bridg:PerformedStudySubjectMilestone.informedConsentIndicator
true
bridg:PerformedStudySubjectMilestone.informedConsentIndicator
Specifies whether the study subject gave official consent by signing the official consent form.
bridg:PerformedStudySubjectMilestone.informedConsentIndicator
Derived from the existence of PerformedStudySubjectMilestone.dateRange WHERE PerformedActivity > DefinedActivity.nameCode = "obtain informed consent".
bridg:PerformedStudySubjectMilestone.informedConsentIndicator
urn:HCTv1.0:CDE_2630147:Recipient_Identification.Consent_for_CIBMTR_related_specimen_repository
bridg:PerformedStudySubjectMilestone.informedConsentIndicator
urn:HCTv1.0:CDE_2532667:Recipient_Identification.Consented_for_Research?
bridg:PerformedStudySubjectMilestone.offStudyDate
offStudyDate
bridg:PerformedStudySubjectMilestone.offStudyDate
true
bridg:PerformedStudySubjectMilestone.offStudyDate
The date (and time) when the study subject is removed from the study.
bridg:PerformedStudySubjectMilestone.offStudyDate
The subject is not being followed and will not be retreated.
bridg:PerformedStudySubjectMilestone.offStudyDate
Derived from PerformedStudySubjectMilestone.dateRange WHERE PerformedActivity > DefinedActivity.nameCode = "remove subject from study".
bridg:PerformedStudySubjectMilestone.offStudyDate
urn:C3PR:StudySubject.offStudyDate
bridg:PerformedStudySubjectMilestone.offStudyDate
urn:C3PRv2.9:StudySubject.offStudyDate
bridg:PerformedStudySubjectMilestone.offStudyDate
urn:CTOM:StudyParticipantAssignment.offStudyDate
bridg:PerformedStudySubjectMilestone.offStudyDate
urn:CTRv1.0:PerformedStudySubjectMilestone.offStudyDate
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
offStudyReasonCode
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
true
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
A coded value specifying why the subject is removed from a study.
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
patient died
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
Derived from PerformedStudySubjectMilestone.reasonCode WHERE PerformedActivity > DefinedActivity.nameCode = "remove subject from study".
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
urn:C3PR:StudySubject.offStudyReasonText
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
urn:C3PRv2.9:StudySubject.offStudyReasonText
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
urn:CTOM:StudyParticipantAssignment.offStudyReasonCode
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
urn:CTOM:StudyParticipantAssignment.offStudyReasonOtherText
bridg:PerformedStudySubjectMilestone.offStudyReasonCode
urn:CTRv1.0:PerformedStudySubjectMilestone.offStudyReasonCode
bridg:PerformedStudySubjectMilestone.registrationDate
registrationDate
bridg:PerformedStudySubjectMilestone.registrationDate
true
bridg:PerformedStudySubjectMilestone.registrationDate
The date (and time) the subject has been registered to the study assuming they have finished screening and have been found eligible.
bridg:PerformedStudySubjectMilestone.registrationDate
Derived from PerformedStudySubjectMilestone.dateRange WHERE PerformedActivity > DefinedActivity.nameCode = "register subject".
bridg:PerformedStudySubjectMilestone.registrationDate
urn:C3PRv2.9:StudySubject.startDate
bridg:PerformedStudySubjectMilestone.registrationDate
urn:CTRPv1.0:PerformedStudySubjectMilestone.registrationDate
bridg:PerformedStudySubjectMilestone.registrationDate
urn:CTRPv3.8:PerformedSubjectMilestone.registrationDate
bridg:PerformedStudySubjectMilestone.registrationDate
urn:CTRv1.0:PerformedStudySubjectMilestone.registrationDate
bridg:PerformedStudySubjectMilestone.registrationDate
urn:LabViewer2.2:SubjectAssignment.onStudyDate
bridg:PerformedStudySubjectMilestone.registrationDate
urn:caAERSv2.2:StudyParticipantAssignment.startDate
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
studyReferenceDateRange
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
true
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
The date and time span used to indicate the start and end of the study for a subject.
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
Derived in two parts. The start date is derived from PerformedStudySubjectMilestone.dateRange WHERE PerformedActivity > DefinedActivity.nameCode = "first intake of agent". The end date is derived from PerformedStudySubjectMilestone.dateRange WHERE PerformedActivity > DefinedActivity.nameCode = "last intake of agent".
These dates are required for all randomized subjects; null for screen failures (if screen failures are submitted).
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:C3PR:StudySubject.startDate
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:CTRv1.0:PerformedStudySubjectMilestone.studyReferenceDateRange
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:SDTM_IGv3.1.1:DM.RFENDTC
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:SDTM_IGv3.1.1:DM.RFSTDTC
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:SDTM_IGv3.1.2:DM.RFENDTC
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:SDTM_IGv3.1.2:DM.RFSTDTC
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:SDTM_IGv3.1.2:AE.AEENTPT
bridg:PerformedStudySubjectMilestone.studyReferenceDateRange
urn:SDTM_IGv3.1.2:MH.MHENTPT
bridg:PerformedSubstanceAdministration.activeIngredientDose
activeIngredientDose
bridg:PerformedSubstanceAdministration.activeIngredientDose
true
bridg:PerformedSubstanceAdministration.activeIngredientDose
The quantity of active ingredients used in a substance administration.
bridg:PerformedSubstanceAdministration.activeIngredientDose
5 mg
bridg:PerformedSubstanceAdministration.activeIngredientDose
Derived by multiplying the PerformedSubstanceAdministration.productDose (the composite product that was administered) with the ProductRelationship.quantity (a ratio) for the component product that is the active ingredient (where ProductRelationship.activeIngredientIndicator = "true").
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CDASHv1.1:EX.EXDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CDASHv1.1:CM.CMDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CDASHv1.1:SU.SUDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CDASHv1.1:EX.EXDSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CTOM:SubstanceAdministration.singleDoseUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CTOM:StudyParticipantAssignment.studyAgentDoseLevel
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CTOM:SubstanceAdministration.singleDose
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CTOM:StudyParticipantAssignment.studyAgentDoseLevelUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:CTRv1.0:PerformedSubstanceAdministration.activeIngredientDose
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.1:CM.CMDOSE
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.1:EX.EXDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.1:EX.EXDOSE
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.1:CM.CMDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.1:SU.SUDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.1:SU.SUDOSE
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.2:CM.CMDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.2:SU.SUDOSE
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.2:EX.EXDOSE
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.2:SU.SUDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.2:EX.EXDOSU
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:SDTM_IGv3.1.2:CM.CMDOSE
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:caAERSv2.2:RadiationIntervention.dosageUnit
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:caAERSv2.2:AdverseEventResponseDescription.reducedDose
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:caAERSv2.2:Dose.amount
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:caAERSv2.2:RadiationIntervention.dosage
bridg:PerformedSubstanceAdministration.activeIngredientDose
urn:caAERSv2.2:Dose.unit
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
activeIngredientDoseDescription
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
false
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
The textual representation of active ingredients in the dosing amounts or a range of dosing information used in a substance administration.
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
200-400
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
This is used for more complex dosages such as scaling and tapering doses, uncertain dosage ranges, differing morning and evening doses and other instructions that can't be expressed with a simple PQ.
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:CDASHv1.1:CM.CMDSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:CDASHv1.1:EX.EXDSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:CDASHv1.1:SU.SUDSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:CTOM:SubstanceAdministration.descriptionText
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:CTRv1.0:PerformedSubstanceAdministration.activeIngredientDoseDescription
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:SDTM_IGv3.1.1:EX.EXDOSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:SDTM_IGv3.1.1:CM.CMDOSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:SDTM_IGv3.1.1:SU.SUDOSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:SDTM_IGv3.1.2:EX.EXDOSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:SDTM_IGv3.1.2:SU.SUDOSTXT
bridg:PerformedSubstanceAdministration.activeIngredientDoseDescription
urn:SDTM_IGv3.1.2:CM.CMDOSTXT
bridg:PerformedSubstanceAdministration.changeReason
changeReason
bridg:PerformedSubstanceAdministration.changeReason
false
bridg:PerformedSubstanceAdministration.changeReason
The rationale for changing the substance administration in relation to the previous substance administration.
bridg:PerformedSubstanceAdministration.changeReason
Dose reduced due to hematologic toxicity
bridg:PerformedSubstanceAdministration.changeReason
urn:CDASHv1.1:EX.EXADJ
bridg:PerformedSubstanceAdministration.changeReason
urn:CTRv1.0:PerformedSubstanceAdministration.changeReason
bridg:PerformedSubstanceAdministration.changeReason
urn:SDTM_IGv3.1.1:EX.EXADJ
bridg:PerformedSubstanceAdministration.changeReason
urn:SDTM_IGv3.1.2:EX.EXADJ
bridg:PerformedSubstanceAdministration.changeTypeCode
changeTypeCode
bridg:PerformedSubstanceAdministration.changeTypeCode
false
bridg:PerformedSubstanceAdministration.changeTypeCode
A coded value specifying the modification of the substance administration in relation to the previous substance administration.
bridg:PerformedSubstanceAdministration.changeTypeCode
Agent Added
bridg:PerformedSubstanceAdministration.changeTypeCode
Agent Dose Decreased
bridg:PerformedSubstanceAdministration.changeTypeCode
Agent Dose Increased
bridg:PerformedSubstanceAdministration.changeTypeCode
urn:CTOM:SubstanceAdministration.doseChangeCode
bridg:PerformedSubstanceAdministration.changeTypeCode
urn:CTRv1.0:PerformedSubstanceAdministration.changeTypeCode
bridg:PerformedSubstanceAdministration.changeTypeCode
urn:caAERSv2.2:CourseAgent.agentAdjustment
bridg:PerformedSubstanceAdministration.distinctProductCount
distinctProductCount
bridg:PerformedSubstanceAdministration.distinctProductCount
false
bridg:PerformedSubstanceAdministration.distinctProductCount
The number of products (resulting from different collections) used for this substance administration.
bridg:PerformedSubstanceAdministration.distinctProductCount
If blood is taken from 2 people (two donations from one of them)
bridg:PerformedSubstanceAdministration.distinctProductCount
this would be counted as 3 different collections.
bridg:PerformedSubstanceAdministration.distinctProductCount
This is a count of distinct donations, typically used for stem cell transplants.
bridg:PerformedSubstanceAdministration.distinctProductCount
urn:HCTv1.0:CDE_2693395:Procedures.Were_multiple_products_infused?
bridg:PerformedSubstanceAdministration.distinctProductCount
urn:HCTv1.0:CDE_3010760:DONOR'.What_is_the_number_of_hematopoietic_stem_cell_products_that_resulted_from_different_collection_methods_or_episodes_and_or_mobilization_techniques?
bridg:PerformedSubstanceAdministration.doseFrequencyCode
doseFrequencyCode
bridg:PerformedSubstanceAdministration.doseFrequencyCode
false
bridg:PerformedSubstanceAdministration.doseFrequencyCode
A coded value specifying how often doses are administered.
bridg:PerformedSubstanceAdministration.doseFrequencyCode
BID
bridg:PerformedSubstanceAdministration.doseFrequencyCode
TID
bridg:PerformedSubstanceAdministration.doseFrequencyCode
QID
bridg:PerformedSubstanceAdministration.doseFrequencyCode
This attribute is needed in order to capture multiple substance administrations in one act, rather than each time a patient swallows a pill, for example "The patient took med X 3 times a day for 10 days starting on June 9th".
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:CDASHv1.1:SU.SUDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:CDASHv1.1:CM.CMDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:CDASHv1.1:EX.EXDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:CTOM:SubstanceAdministration.doseFrequencyText
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:CTOM:SubstanceAdministration.doseFrequencyCode
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:CTRv1.0:PerformedSubstanceAdministration.doseFrequencyCode
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:NCI_CRF_Standard:CDE_2003322v4.0:_Administration_Schedule_Term_Name
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.1:SU.SUDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.1:CM.CMDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.1:EX.EXDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.2:SU.SUDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.2:EX.EXDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:SDTM_IGv3.1.2:CM.CMDOSFRQ
bridg:PerformedSubstanceAdministration.doseFrequencyCode
urn:caAERSv2.2:CourseAgent.durationAndSchedule
bridg:PerformedSubstanceAdministration.dosePeriodCode
dosePeriodCode
bridg:PerformedSubstanceAdministration.dosePeriodCode
false
bridg:PerformedSubstanceAdministration.dosePeriodCode
A coded value specifying the period during which the dose total is administered.
bridg:PerformedSubstanceAdministration.dosePeriodCode
daily
bridg:PerformedSubstanceAdministration.dosePeriodCode
course
bridg:PerformedSubstanceAdministration.dosePeriodCode
The dose total is defined in periodProductDoseTotal and/or periodActiveIngredientDoseTotal.
bridg:PerformedSubstanceAdministration.dosePeriodCode
urn:CTRv1.0:PerformedSubstanceAdministration.dosePeriodCode
bridg:PerformedSubstanceAdministration.dosePeriodCode
urn:HCTv1.0:CDE_2635420:Therapy_Doses.Was_the_radiation_therapy_fractionated
bridg:PerformedSubstanceAdministration.dosePeriodCode
urn:caAERSv2.2:CourseAgent_totalDoseAdministeredThisCourse_Dose
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
endRelativeToReferenceCode
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
true
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
A coded value specifying when this event ended with respect to the sponsor-defined reference period.
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
before
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
during
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
during/after
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
after
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
Derived from comparing PerformedSubstanceAdministration.dateRange(IVL<TS.DATETIME>).high and PerformedStudySubjectMilestone.studyReferenceDateRange.
Sponsors should define the reference period in the study metadata.
This may be populated when a start date is not collected.
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
urn:CTRv1.0:PerformedSubstanceAdministration.endRelativeToReferenceCode
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
urn:SDTM_IGv3.1.1:CM.CMENRF
bridg:PerformedSubstanceAdministration.endRelativeToReferenceCode
urn:SDTM_IGv3.1.1:SU.SUENRF
bridg:PerformedSubstanceAdministration.flowRate
flowRate
bridg:PerformedSubstanceAdministration.flowRate
false
bridg:PerformedSubstanceAdministration.flowRate
A ratio specifying the speed with which the substance is introduced into the subject.
bridg:PerformedSubstanceAdministration.flowRate
100 mL/h
bridg:PerformedSubstanceAdministration.flowRate
1 g/d
bridg:PerformedSubstanceAdministration.flowRate
40 mmol/h
bridg:PerformedSubstanceAdministration.flowRate
urn:CDASHv1.1:EX.EXFLRT
bridg:PerformedSubstanceAdministration.flowRate
urn:CDASHv1.1:EX.EXFLRTU
bridg:PerformedSubstanceAdministration.flowRate
urn:CTRv1.0:PerformedSubstanceAdministration.flowRate
bridg:PerformedSubstanceAdministration.flowRate
urn:FDA_HL7_SD_SD_DSTU2012:PlannedSubjectActivity/SubstanceAdministration.rateQuantity
bridg:PerformedSubstanceAdministration.flowRate
urn:NCI_CRF_Standard:CDE_2475888v1.0:_Infusion_Flow_Rate_Number
bridg:PerformedSubstanceAdministration.interruptionDuration
interruptionDuration
bridg:PerformedSubstanceAdministration.interruptionDuration
false
bridg:PerformedSubstanceAdministration.interruptionDuration
The period of time during which a substance administration is interrupted.
bridg:PerformedSubstanceAdministration.interruptionDuration
An infusion started at 12:15pm and ended at 2:37pm
bridg:PerformedSubstanceAdministration.interruptionDuration
but there was an interruption of 17 minutes.
bridg:PerformedSubstanceAdministration.interruptionDuration
urn:CDASHv1.1:EX.EXINTRPU
bridg:PerformedSubstanceAdministration.interruptionDuration
urn:CDASHv1.1:EX.EXINTRP
bridg:PerformedSubstanceAdministration.interruptionDuration
urn:CTRv1.0:PerformedSubstanceAdministration.interruptionDuration
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
periodActiveIngredientDoseTotal
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
true
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
The total amount of active ingredient in all doses of treatment in a given period of time.
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
The given period of time is defined in dosePeriodCode.
Derived by multiplying PerformedSubstanceAdministration.periodProductDoseTotal (the composite product that was administered) with the ProductRelationship.quantity (a ratio) for the component product that is the active ingredient (where ProductRelationship.activeIngredientIndicator = "true").
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:CDASHv1.1:CM.CMDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:CTOM:SubstanceAdministration.totalDose
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:CTOM:SubstanceAdministration.totalDoseUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:CTRv1.0:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:SDTM_IGv3.1.1:CM.CMDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:SDTM_IGv3.1.1:SU.SUDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:SDTM_IGv3.1.1:EX.EXDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:SDTM_IGv3.1.2:EX.EXDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:SDTM_IGv3.1.2:SU.SUDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:SDTM_IGv3.1.2:CM.CMDOSTOT
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:caAERSv2.2:Dose.amount
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:caAERSv2.2:Dose.units
bridg:PerformedSubstanceAdministration.periodActiveIngredientDoseTotal
urn:caAERSv2.2:RadiationIntervention.fractionNumber
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
periodProductDoseTotal
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
false
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
The total of all doses of treatment in a given period of time.
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
The given period of time is defined in dosePeriodCode.
This attribute, periodProductDoseTotal, is not necessarily derivable since the dose may be provided as a string (in productDoseDescription).
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:CTOM:SubstanceAdministration.totalDoseUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:CTOM:SubstanceAdministration.totalDose
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:CTRv1.0:PerformedSubstanceAdministration.periodProductDoseTotal
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960649:Therapies.Specify_gamma_knife_and/or_radiosurgery_radiation_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2953815:Therapies.Total_dose_unit_of_measure:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_3181110:Therapies.Therapeutic_procedure_administered_milligram_daily_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2721441:Therapies.Total_Dose
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960635:Therapies.Specify_local_cranial_radiation_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2964435:Therapies.Radiation_therapy_field_radioactive_instillation_total_dose
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2980940:Therapies.What_was_the_radiation_total_dose?
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2979333:Therapies.Local-regional_radiation_therapy_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960642:Therapies.Specify_craniospinal_radiation_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2962200:Therapies.Specify_interstitial_irradiation/brachytherapy_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_3086792:Therapies.Specify_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960770:Therapies.Specify_the_total_radiation_dose_administered_to_another_site:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960298:Therapies.What_was_the_preparative_regimen_total_milligram_dose?
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960618:Therapies.Specify_whole_brain_radiation_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:HCTv1.0:CDE_2960768:Therapies.Specify_local_spinal_radiation_total_dose:
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:caAERSv2.2:Dose.units
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:caAERSv2.2:RadiationIntervention.fractionNumber
bridg:PerformedSubstanceAdministration.periodProductDoseTotal
urn:caAERSv2.2:Dose.amount
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
plannedChangeIndicator
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
false
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
Specifies whether a change in the substance administration in relation to the previous substance administration is planned or not.
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
True = planned
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
False = unplanned
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
urn:CTOM:DiseaseResponse.doseChangeIndicatorCode
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
urn:CTOM:SubstanceAdministration.doseChangeIndicatorCode
bridg:PerformedSubstanceAdministration.plannedChangeIndicator
urn:CTRv1.0:PerformedSubstanceAdministration.plannedChangeIndicator
bridg:PerformedSubstanceAdministration.productDose
productDose
bridg:PerformedSubstanceAdministration.productDose
false
bridg:PerformedSubstanceAdministration.productDose
The quantity of a substance or medication used in a substance administration.
bridg:PerformedSubstanceAdministration.productDose
5 mg
bridg:PerformedSubstanceAdministration.productDose
DefinedSubstanceAdministration.productDose can contain a dose expressed in absolute or relative terms (e.g., mg or mg/kg). ScheduledSubstanceAdministration.activeIngredientDose and PerformedSubstanceAdministration.productDose must contain a dose expressed in absolute terms (e.g., mg). If the DefinedSubstanceAdministration.productDose was expressed in relative terms (e.g., mg/kg), then the absolute dose must have been calculated using one or more observed factors as identified by the DefinedExpressionVariableRelationship.
bridg:PerformedSubstanceAdministration.productDose
urn:CDASHv1.1:EX.EXVOLT
bridg:PerformedSubstanceAdministration.productDose
urn:CDASHv1.1:EX.EXVOLTU
bridg:PerformedSubstanceAdministration.productDose
urn:CTOM:Radiation.doseUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.productDose
urn:CTOM:StudyParticipantAssignment.studyAgentDoseLevelUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.productDose
urn:CTOM:SubstanceAdministration.singleDoseUnitOfMeasureCode
bridg:PerformedSubstanceAdministration.productDose
urn:CTOM:Radiation.dose
bridg:PerformedSubstanceAdministration.productDose
urn:CTOM:StudyParticipantAssignment.studyAgentDoseLevel
bridg:PerformedSubstanceAdministration.productDose
urn:CTOM:SubstanceAdministration.singleDose
bridg:PerformedSubstanceAdministration.productDose
urn:CTRv1.0:PerformedSubstanceAdministration.productDose
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2729014:Therapies.For_the_allogeneic_blood_transfusion__specify_the_number_of_units:
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_3108427:Therapies.What_is_the_dose_value_of_the_preparative_regimen_medication?
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2738560:Therapy_Doses.Total_volume_of_product_plus_additives_infused:
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2180757:Therapies.RT_Dose_per_Fraction
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2954034:Therapy_Doses.Dose_per_fraction_unit_of_measure:
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2729000:Therapies.For_the_autologous_blood_transfusion__specify_the_number_of_units:
bridg:PerformedSubstanceAdministration.productDose
urn:HCTv1.0:CDE_2954032:Therapy_Doses.Dose_per_fraction:
bridg:PerformedSubstanceAdministration.productDose
urn:NCI_CRF_Standard:CDE_2182728v2.0:_Agent_Dose
bridg:PerformedSubstanceAdministration.productDose
urn:NCI_CRF_Standard:CDE_3028750v1.0:_Intervention_Potency_Unit_of_Measure_for_Unified_Code_for_Units_of_Measure_Code
bridg:PerformedSubstanceAdministration.productDose
urn:caAERSv2.2:RadiationIntervention.dosage
bridg:PerformedSubstanceAdministration.productDose
urn:caAERSv2.2:Dose.unit
bridg:PerformedSubstanceAdministration.productDose
urn:caAERSv2.2:RadiationIntervention.dosageUnit
bridg:PerformedSubstanceAdministration.productDose
urn:caAERSv2.2:Dose.amount
bridg:PerformedSubstanceAdministration.productDose
urn:caAERSv2.2:AdverseEventResponseDescription.reducedDose
bridg:PerformedSubstanceAdministration.productDoseDescription
productDoseDescription
bridg:PerformedSubstanceAdministration.productDoseDescription
false
bridg:PerformedSubstanceAdministration.productDoseDescription
The textual representation of dosing amounts or a range of dosing information used in a substance administration.
bridg:PerformedSubstanceAdministration.productDoseDescription
200-400
bridg:PerformedSubstanceAdministration.productDoseDescription
This is used for more complex dosages such as scaling and tapering doses, uncertain dosage ranges, differing morning and evening doses and other instructions that can't be expressed with a simple PQ.
bridg:PerformedSubstanceAdministration.productDoseDescription
urn:CTOM:SubstanceAdministration.descriptionText
bridg:PerformedSubstanceAdministration.productDoseDescription
urn:CTRv1.0:PerformedSubstanceAdministration.productDoseDescription
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
routeOfAdministrationCode
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
false
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
A coded value specifying the physiological path or method of introducing the substance into or onto the subject.
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
oral
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
intravenous
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
swallow
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
oral rinse
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
oral topical application
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
chew
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
oral dissolve
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
oral inhalation
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
Route is more than just approach site. It deals with how the body will actually absorb/receive the drug. The approach site might be "mouth", but from a route code perspective, this could include: swallow, oral rinse, oral topical application, chew, oral dissolve, oral inhalation (via intermittent flow or rebreather mask). The effect of the drug could vary depending on the route even if the body site happens to be the same.
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:CDASHv1.1:EX.EXROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:CDASHv1.1:CM.CMROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:CTOM:SubstanceAdministration.routeCode
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:CTRv1.0:PerformedSubstanceAdministration.routeOfAdministrationCode
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:HCTv1.0:MD_Anderson_Specific_Content:_Transplant.Intravenous_administration
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:HCTv1.0:CDE_2780200:Therapy_Doses.Specify_route_of_infusion:
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:HCTv1.0:CDE_2698088:Therapy_Doses.Specify_the_route_of_product_infusion:
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:HCTv1.0:CDE_2960396:Therapies.What_was_the_route_of_administration_for_the_preparative_regimen_drugs?
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:NCI_CRF_Standard:CDE_2003586v6.0:_Access_Route_of_Administration_Text_Code
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.1:CM.CMROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.1:EX.EXROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.1:SU.SUROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.2:CM.CMROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.2:SU.SUROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:SDTM_IGv3.1.2:EX.EXROUTE
bridg:PerformedSubstanceAdministration.routeOfAdministrationCode
urn:caAERSv2.2:Dose.route
bridg:PerformedSubstanceAdministration.standardTimeIndicator
standardTimeIndicator
bridg:PerformedSubstanceAdministration.standardTimeIndicator
false
bridg:PerformedSubstanceAdministration.standardTimeIndicator
Specifies whether the time of the substance administration is specified using standard (as opposed to daylight savings) time.
bridg:PerformedSubstanceAdministration.standardTimeIndicator
If the location and date are known, this data is derivable.
bridg:PerformedSubstanceAdministration.standardTimeIndicator
urn:HCTv1.0:CDE_2713223:Occurrences.Is_it_the_standard_time_or_daylight_savings_time?
bridg:PerformedSubstanceAdministration.standardTimeIndicator
urn:HCTv1.0:CDE_2713225:Occurrences.Is_it_the_standard_time_or_daylight_savings_time?
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
startRelativeToReferenceCode
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
true
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
A coded value specifying when this event started with respect to the sponsor-defined reference period.
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
Medications that are ongoing at the end of the reference period should have a value of "during/after" for this variable.
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
Before
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
during
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
during/after
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
after
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
Derived from comparing PerformedSubstanceAdministration.dateRange(IVL<TS.DATETIME).low and PerformedStudySubjectMilestone.studyReferenceDateRange.
Sponsors should define the reference period in the study metadata.
This may be populated when a start date is not collected.
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
urn:CTRv1.0:PerformedSubstanceAdministration.startRelativeToReferenceCode
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
urn:SDTM_IGv3.1.1:SU.SUSTRF
bridg:PerformedSubstanceAdministration.startRelativeToReferenceCode
urn:SDTM_IGv3.1.1:CM.CMSTRF
bridg:PerformedSubstanceAdministration.substanceUnknownIndicator
substanceUnknownIndicator
bridg:PerformedSubstanceAdministration.substanceUnknownIndicator
false
bridg:PerformedSubstanceAdministration.substanceUnknownIndicator
Specifies whether the substance administered was not known.
bridg:PerformedSubstanceAdministration.substanceUnknownIndicator
urn:HCTv1.0:CDE_2974124:Therapies.What_is_the_reason_for_the_drug_induced_drug_missing_value?
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
treatmentVehicleQuantity
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
true
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
The quantity and units of treatment vehicle used.
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
10 milligrams
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
2 milliliters
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
Derived by multiplying the
PerformedSubstancedAdministration.productDose (the composite product that was administered) with the ProductRelationship.quantity
(a ratio) for the component product that is the active ingredient (where ProductRelationship.activeIngredientIndicator = "false").
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
urn:CTRPv1.0:SubstanceAdministration.treatmentVehicleVolume
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
urn:NCI_CRF_Standard:CDE_2871633v1.0:_Agent_Administration_Drug_Vehicle_Total_Volume_Number
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
urn:SDTM_IGv3.1.2:EX.EXVAMTU
bridg:PerformedSubstanceAdministration.treatmentVehicleQuantity
urn:SDTM_IGv3.1.2:EX.EXVAMT
bridg:Performer.effectiveDateRange
effectiveDateRange
bridg:Performer.effectiveDateRange
false
bridg:Performer.effectiveDateRange
The date (and time) span for when the performer is active.
bridg:Performer.effectiveDateRange
urn:CTRv1.0:Performer.effectiveDateRange
Universal
bridg:Performer.effectiveDateRange
urn:HL7SD:R_AssignedEntity
bridg:Performer.identifier
identifier
bridg:Performer.identifier
false
bridg:Performer.identifier
A unique symbol that establishes identity of the performer.
bridg:Performer.identifier
urn:CTRv1.0:Performer.identifier
Universal
bridg:Performer.identifier
urn:HL7SD:R_AssignedEntity
bridg:Performer.postalAddress
postalAddress
bridg:Performer.postalAddress
false
bridg:Performer.postalAddress
A contact point used to send physical forms of communication to the performer.
bridg:Performer.postalAddress
urn:CTRv1.0:Performer.postalAddress
Universal
bridg:Performer.postalAddress
urn:HL7SD:R_AssignedEntity
in IndividualCaseSafetyReport
bridg:Performer.postalAddress
urn:ICSRr2:AssignedEntity.addr
bridg:Performer.telecomAddress
telecomAddress
bridg:Performer.telecomAddress
false
bridg:Performer.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the performer.
bridg:Performer.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:Performer.telecomAddress
urn:CTRv1.0:Performer.telecomAddress
bridg:Performer.telecomAddress
urn:HCTv1.0:CDE_2518194:Individuals.Outside_Contact_Phone_Number
Universal
bridg:Performer.telecomAddress
urn:HL7SD:R_AssignedEntity
in IndividualCaseSafetyReport
bridg:Performer.telecomAddress
urn:ICSRr2:AssignedEntity.telecom
bridg:Performer.telecomAddress
urn:caAERSv2.2:PlannedEmailNotification.from
bridg:Performer.typeCode
typeCode
bridg:Performer.typeCode
false
bridg:Performer.typeCode
A coded value specifying the kind of performer.
bridg:Performer.typeCode
surgeon
bridg:Performer.typeCode
monitoring device
bridg:Performer.typeCode
performing laboratory
bridg:Performer.typeCode
urn:AE:PerformingParty.roleType
bridg:Performer.typeCode
urn:CDASHv1.1:PE.PEEVAL
bridg:Performer.typeCode
urn:CTR_Rr2:Responsible_Site_Role
bridg:Performer.typeCode
urn:CTRRr3:Performer.typeCode
bridg:Performer.typeCode
urn:CTRv1.0:Performer.typeCode
in R_Product
bridg:Performer.typeCode
urn:ICSRr2:author.typeCode
in IndividualCaseSafetyReport
bridg:Performer.typeCode
urn:ICSRr2:AssignedEntity.code
in R_Product
bridg:Performer.typeCode
urn:ICSRr2:performer.typeCode
bridg:Performer.typeCode
urn:SDTM_IGv3.1.1:EG.EGEVAL
bridg:Performer.typeCode
urn:SDTM_IGv3.1.1:PE.PEEVAL
bridg:Performer.typeCode
urn:SDTM_IGv3.1.1:CO.COEVAL
bridg:Performer.typeCode
urn:SDTM_IGv3.1.2:CO.COEVAL
bridg:Performer.typeCode
urn:SDTM_IGv3.1.2:EG.EGEVAL
bridg:Performer.typeCode
urn:SDTM_IGv3.1.2:FA.FAEVAL
bridg:Performer.typeCode
urn:SDTM_IGv3.1.2:PE.PEEVAL
bridg:Person.educationLevelCode
educationLevelCode
bridg:Person.educationLevelCode
false
bridg:Person.educationLevelCode
A coded value specifying the highest level of education completed.
bridg:Person.educationLevelCode
Less than High School Diploma
bridg:Person.educationLevelCode
High School Diploma
bridg:Person.educationLevelCode
Some College
bridg:Person.educationLevelCode
urn:CDASHv1.1:SC.SCORRES
bridg:Person.educationLevelCode
urn:CTOM:Investigator.educationLevelCode
bridg:Person.educationLevelCode
urn:CTOM:Participant.educationLevelCode
bridg:Person.educationLevelCode
urn:CTOM:Person.educationLevelCode
bridg:Person.educationLevelCode
urn:CTRv1.0:Person.educationLevelCode
bridg:Person.educationLevelCode
urn:HCTv1.0:CDE_2815244:Property_or_Attribute.Education_level
bridg:Person.educationLevelCode
urn:NCI_CRF_Standard:CDE_2681552v1.0:_Person_Education_Level_Summary_Type
bridg:Person.educationLevelCode
urn:NCI_CRF_Standard:CDE_2674076v2.0:_Person_Education_Level_Type
bridg:Person.educationLevelCode
urn:SDTM_IGv3.1.2:SC.SCSTRESC
bridg:Person.educationLevelCode
urn:SDTM_IGv3.1.2:SC.SCORRES
bridg:Person.ethnicGroupCode
ethnicGroupCode
bridg:Person.ethnicGroupCode
false
bridg:Person.ethnicGroupCode
A coded value specifying the self-declared ethnic origination, independent of racial origination.
bridg:Person.ethnicGroupCode
Office of Management and Budget (OMB) approved categories [example from National Cancer Insitute]
bridg:Person.ethnicGroupCode
urn:C3PR:Participant.ethnicGroup
bridg:Person.ethnicGroupCode
urn:C3PRv2.9:Participant.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:CDASHv1.1:DM.ETHNIC
bridg:Person.ethnicGroupCode
urn:CTOM:Investigator.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:CTOM:Person.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:CTOM:Participant.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:CTRPv3.8:Person.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:CTRv1.0:Person.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:HCTv1.0:CDE_3186998:Physical_Description_of_Individuals.What_is_the_patient's_ethnic_group?
bridg:Person.ethnicGroupCode
urn:HCTv1.0:CDE_2769672:Individuals.Donor's_ethnicity:
bridg:Person.ethnicGroupCode
urn:HCTv1.0:CDE_2002440:Recipient_Identification.Ethnicity
in IndividualCaseSafetyReport
bridg:Person.ethnicGroupCode
urn:ICSRr2:Person2.ethnicGroupCode
bridg:Person.ethnicGroupCode
urn:NCI_CRF_Standard:CDE_2192217v2.0:_Ethnic_Group_Category_Text
bridg:Person.ethnicGroupCode
urn:NCI_CRF_Standard:CDE_2200284v2.0:_Centers_for_Disease_Control_and_Prevention_Ethnicity_Unique_Identifier_Codes
bridg:Person.ethnicGroupCode
urn:SDTM_IGv3.1.1:DM.ETHNIC
bridg:Person.ethnicGroupCode
urn:SDTM_IGv3.1.2:DM.ETHNIC
bridg:Person.ethnicGroupCode
urn:caAERSv2.2:Participant.ethnicity
bridg:Person.initials
initials
bridg:Person.initials
false
bridg:Person.initials
The first letters of the person's first name, middle name, and last name.
bridg:Person.initials
If the person does not have a middle name or initial, the initials will only be two characters.
bridg:Person.initials
urn:CTOM:Participant.initials
bridg:Person.initials
urn:CTRv1.0:Person.initials
bridg:Person.initials
urn:Lab:Person.initials
bridg:Person.initials
urn:Lab:Participant.initials
bridg:Person.initials
urn:Lab:Investigator.initials
bridg:Person.initials
urn:LabViewer2.2:Person.initials
bridg:Person.initials
urn:LabViewer2.2:Participant.initials
bridg:Person.initials
urn:LabViewer2.2:Investigator.initials
bridg:Person.initials
urn:NCI_CRF_Standard:CDE_2001039v4.0:_Patient_Initials_Name
bridg:Person.maritalStatusCode
maritalStatusCode
bridg:Person.maritalStatusCode
false
bridg:Person.maritalStatusCode
A coded value specifying the domestic partnership status of a person.
bridg:Person.maritalStatusCode
Married
bridg:Person.maritalStatusCode
Widowed
bridg:Person.maritalStatusCode
Single
bridg:Person.maritalStatusCode
Separated
bridg:Person.maritalStatusCode
urn:C3PR:Participant.maritalStatusCode
bridg:Person.maritalStatusCode
urn:C3PRv2.9:Participant.maritalStatusCode
bridg:Person.maritalStatusCode
urn:CDASHv1.1:SC.SCORRES
bridg:Person.maritalStatusCode
urn:CTOM:Participant.maritalStatusCode
bridg:Person.maritalStatusCode
urn:CTOM:Investigator.maritalStatusCode
bridg:Person.maritalStatusCode
urn:CTOM:Person.maritalStatusCode
bridg:Person.maritalStatusCode
urn:CTRv1.0:Person.maritalStatusCode
bridg:Person.maritalStatusCode
urn:HCTv1.0:CDE_2815107:Individuals.What_is_the_marital_status_of_the_person?
bridg:Person.maritalStatusCode
urn:NCI_CRF_Standard:CDE_2188083v2.0:_Person_Marital_Status_Category
bridg:Person.maritalStatusCode
urn:SDTM_IGv3.1.2:SC.SCSTRESC
bridg:Person.maritalStatusCode
urn:SDTM_IGv3.1.2:SC.SCORRES
bridg:Person.occupationDateRange
occupationDateRange
bridg:Person.occupationDateRange
false
bridg:Person.occupationDateRange
The date (and time) span specifying the start and end of a person's occupation.
bridg:Person.occupationDateRange
The occupation is determined by the Person.primaryOccupationCode.
bridg:Person.occupationDateRange
urn:CTOM:PersonOccupation.startDate
bridg:Person.occupationDateRange
urn:CTOM:PersonOccupation.stopDate
bridg:Person.occupationDateRange
urn:CTRv1.0:Person.occupationDateRange
bridg:Person.postalAddress
postalAddress
bridg:Person.postalAddress
false
bridg:Person.postalAddress
A contact point used to send physical forms of communication to the person.
bridg:Person.postalAddress
urn:C3PR:Address.countryCode
bridg:Person.postalAddress
urn:C3PR:Address.cityCode
bridg:Person.postalAddress
urn:C3PR:Address.stateCode
bridg:Person.postalAddress
urn:C3PR:Address.postalCode
bridg:Person.postalAddress
urn:C3PR:ContactMechanism.type
bridg:Person.postalAddress
urn:C3PR:Address.streetAddress
bridg:Person.postalAddress
urn:C3PR:ContactMechanism.value
bridg:Person.postalAddress
urn:C3PRv2.9:Address
bridg:Person.postalAddress
urn:CTOM:Participant.state
bridg:Person.postalAddress
urn:CTOM:Investigator.streetAddress
bridg:Person.postalAddress
urn:CTOM:Investigator.zipCode
bridg:Person.postalAddress
urn:CTOM:Person.state
bridg:Person.postalAddress
urn:CTOM:Investigator.state
bridg:Person.postalAddress
urn:CTOM:Person.streetAddress
bridg:Person.postalAddress
urn:CTOM:Person.city
bridg:Person.postalAddress
urn:CTOM:Participant.zipCode
bridg:Person.postalAddress
urn:CTOM:Participant.countryCode
bridg:Person.postalAddress
urn:CTOM:Investigator.countryCode
bridg:Person.postalAddress
urn:CTOM:Participant.streetAddress
bridg:Person.postalAddress
urn:CTOM:Person.zipCode
bridg:Person.postalAddress
urn:CTOM:Person.countryCode
bridg:Person.postalAddress
urn:CTOM:Investigator.city
bridg:Person.postalAddress
urn:CTOM:Participant.city
bridg:Person.postalAddress
urn:CTRPv1.0:Person.postalAddress
bridg:Person.postalAddress
urn:CTRPv3.8:Person.postalAddress
bridg:Person.postalAddress
urn:CTRRr3:Person.postalAddress
bridg:Person.postalAddress
urn:CTRv1.0:Person.postalAddress
bridg:Person.postalAddress
urn:HCTv1.0:CDE_2797876:Geographic_Locations.Country_of_residence:
bridg:Person.postalAddress
urn:HCTv1.0:CDE_3119139:Geographic_Locations.City
bridg:Person.postalAddress
urn:HCTv1.0:CDE_2816450:Geographic_Locations.Specify_other_country:
bridg:Person.postalAddress
urn:HCTv1.0:CDE_2797862:Geographic_Locations.US_state_of_residence:
bridg:Person.postalAddress
urn:HCTv1.0:CDE_2179603:Geographic_Locations.State
in IndividualCaseSafetyReport
bridg:Person.postalAddress
urn:ICSRr2:AssignedEntity.addr
in R_Product
bridg:Person.postalAddress
urn:ICSRr2:AssignedEntity2.addr
in IndividualCaseSafetyReport
bridg:Person.postalAddress
urn:ICSRr2:Person2.addr
in IndividualCaseSafetyReport
bridg:Person.postalAddress
urn:ICSRr2:ContactParty2.addr
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_62587v3.0:_Street_Address
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_2179606v2.0:_Address_Postal_Code_Identifier
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_2179603v2.0:_Address_State/Province_Name
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_315v4.0:_Person_Address_Country_Name
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_2943243v1.0:_Person_Enrollment_Address_United_States_Integer::2000_Census_Tract_Code
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_2179606v2.0:_Address_Postal_Code_Identifier
bridg:Person.postalAddress
urn:NCI_CRF_Standard:CDE_2179601v1.0:_Address_City_Name
bridg:Person.postalAddress
urn:caAERSv2.2:Address.country___PersonContact
bridg:Person.postalAddress
urn:caAERSv2.2:Address.street___PersonContact
bridg:Person.postalAddress
urn:caAERSv2.2:Address.state___ResearchStaff
bridg:Person.postalAddress
urn:caAERSv2.2:Address.city___PersonContact
bridg:Person.postalAddress
urn:caAERSv2.2:Address.zip__PersonContact
bridg:Person.primaryOccupationCode
primaryOccupationCode
bridg:Person.primaryOccupationCode
false
bridg:Person.primaryOccupationCode
A coded value specifying the principal activity that a person does to earn money.
bridg:Person.primaryOccupationCode
urn:CDASHv1.1:SC.SCORRES
bridg:Person.primaryOccupationCode
urn:CTOM:PersonOccupation.primaryTypeCodeSystem
bridg:Person.primaryOccupationCode
urn:CTOM:PersonOccupation.primaryTypeCode
bridg:Person.primaryOccupationCode
urn:CTRv1.0:Person.primaryOccupationCode
bridg:Person.primaryOccupationCode
urn:HCTv1.0:CDE_2222677:Jobs.Other
bridg:Person.primaryOccupationCode
urn:HCTv1.0:CDE_2815112:Jobs.What_category_best_describes_the_occupation_of_the_person?
bridg:Person.primaryOccupationCode
urn:HCTv1.0:CDE_2798174:Personal_attributes.What_is_the_current_or_most_recent_work_status?
bridg:Person.primaryOccupationCode
urn:SDTM_IGv3.1.2:SC.SCORRES
bridg:Person.primaryOccupationCode
urn:SDTM_IGv3.1.2:SC.SCSTRESC
bridg:Person.raceCode
raceCode
bridg:Person.raceCode
false
bridg:Person.raceCode
A coded value specifying a self-declared racial origination, independent of ethnic origination.
bridg:Person.raceCode
Office of Management and Budget (OMB) approved categories [example from National Cancer Insitute]
bridg:Person.raceCode
urn:C3PR:Participant.raceCode
bridg:Person.raceCode
urn:C3PRv2.9:Participant.raceCode
bridg:Person.raceCode
urn:CDASHv1.1:DM.RACE
bridg:Person.raceCode
urn:CDASHv1.1:DM.RACEOTH
bridg:Person.raceCode
urn:CTOM:Person.raceCode
bridg:Person.raceCode
urn:CTOM:Participant.raceCode
bridg:Person.raceCode
urn:CTOM:Investigator.raceCode
bridg:Person.raceCode
urn:CTRPv1.0:Person.raceCode
bridg:Person.raceCode
urn:CTRPv3.8:Person.raceCode
bridg:Person.raceCode
urn:CTRv1.0:Person.raceCode
bridg:Person.raceCode
urn:HCTv1.0:CDE_2786681:Personal_attributes.Donor's_race
bridg:Person.raceCode
urn:HCTv1.0:CDE_106_//_:Recipient_Identification.Race
bridg:Person.raceCode
urn:HCTv1.0:CDE_2798213:UML_DEFAULT_CD.Race_group_the_person_belongs_to:
in IndividualCaseSafetyReport
bridg:Person.raceCode
urn:ICSRr2:Person2.raceCode
bridg:Person.raceCode
urn:LabViewer2.2:ParticipantRace.codeSystemVersion
bridg:Person.raceCode
urn:LabViewer2.2:ParticipantRace.codeSystem
bridg:Person.raceCode
urn:LabViewer2.2:ParticipantRace.code
bridg:Person.raceCode
urn:LabViewer2.2:ParticipantRace.codeSystemName
bridg:Person.raceCode
urn:LabViewer2.2:ParticipantRace.displayName
bridg:Person.raceCode
urn:NCI_CRF_Standard:CDE_2192199v1.0:_Race_Category_Text
bridg:Person.raceCode
urn:NCI_CRF_Standard:CDE_2200286v1.0:_Centers_for_Disease_Control_and_Prevention_Race_Unique_Identifier_Code
bridg:Person.raceCode
urn:SDTM_IGv3.1.1:DM.RACE
bridg:Person.raceCode
urn:SDTM_IGv3.1.2:DM.RACE
bridg:Person.raceCode
urn:caAERSv2.2:Participant.race
bridg:Person.telecomAddress
telecomAddress
bridg:Person.telecomAddress
false
bridg:Person.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the person.
bridg:Person.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:Person.telecomAddress
urn:C3PR:ContactMechanism.value
bridg:Person.telecomAddress
urn:C3PR:ContactMechanism.type
bridg:Person.telecomAddress
urn:C3PRv2.9:ContactMechanism.value
bridg:Person.telecomAddress
urn:C3PRv2.9:ContactMechanism.type
bridg:Person.telecomAddress
urn:C3PRv2.9:ContactMechanismBasedRecipient
bridg:Person.telecomAddress
urn:C3PRv2.9:ReportVersion.email
bridg:Person.telecomAddress
urn:CTOM:Investigator.telecomAddress
bridg:Person.telecomAddress
urn:CTOM:Person.telecomAddress
bridg:Person.telecomAddress
urn:CTOM:Person.phone
bridg:Person.telecomAddress
urn:CTOM:Investigator.phone
bridg:Person.telecomAddress
urn:CTOM:Participant.telecomAddress
bridg:Person.telecomAddress
urn:CTOM:Participant.phone
bridg:Person.telecomAddress
urn:CTRPv1.0:Person.telecomAddress
bridg:Person.telecomAddress
urn:CTRPv3.8:Person.telecomAddress
bridg:Person.telecomAddress
urn:CTRRr3:Person.telecomAddress
bridg:Person.telecomAddress
urn:CTRv1.0:Person.telecomAddress
bridg:Person.telecomAddress
urn:HCTv1.0:CDE_2828513:Individuals.Telephone_number:
bridg:Person.telecomAddress
urn:HCTv1.0:CDE_2828511:Individuals.Fax_number:
bridg:Person.telecomAddress
urn:HCTv1.0:CDE_58319//:Telecommunications.Fax_Number
in IndividualCaseSafetyReport
bridg:Person.telecomAddress
urn:ICSRr2:AssignedEntity.telecom
in IndividualCaseSafetyReport
bridg:Person.telecomAddress
urn:ICSRr2:Person2.telecom
in IndividualCaseSafetyReport
bridg:Person.telecomAddress
urn:ICSRr2:ContactParty2.telecom
in R_Product
bridg:Person.telecomAddress
urn:ICSRr2:AssignedEntity2.telecom
bridg:Person.telecomAddress
urn:NCI_CRF_Standard:CDE_2179593v3.0:_Telephone_Number
bridg:Person.telecomAddress
urn:NCI_CRF_Standard:CDE_2179594v4.0:_Telephone_Number_Type
bridg:Person.telecomAddress
urn:caAERSv2.2:ScheduledEmailNotification.to
bridg:Person.telecomAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:Person.telecomAddress
urn:caAERSv2.2:PersonContact.ReportPerson.Reporter.contactMechanisms
bridg:Person.telecomAddress
urn:caAERSv2.2:User.emailAddress
bridg:Person.telecomAddress
urn:caAERSv2.2:ReportDelivery.address
bridg:Place.identifier
identifier
bridg:Place.identifier
false
bridg:Place.identifier
A unique symbol that establishes identity of the place.
bridg:Place.identifier
The license plate number of an ambulance
bridg:Place.identifier
an identifier for a bed in a hospital ward
bridg:Place.identifier
urn:BRIDGSCC:Model_Integrity
bridg:Place.identifier
urn:CTRv1.0:Place.identifier
bridg:Place.identifierCode
identifierCode
bridg:Place.identifierCode
false
bridg:Place.identifierCode
A coded value uniquely specifying the place.
bridg:Place.identifierCode
United States (US)
bridg:Place.identifierCode
European Union (EU)
bridg:Place.identifierCode
jurisdiction territory code
bridg:Place.identifierCode
The only current use case for this attribute is to specify the geographical area an authority has to make laws and enforce them. For example, the Food and Drug Administration (FDA) exercises responsibility for pharmacovigilance (RegulatoryAuthority.jurisdictionAuthorityCode) in the United States (Place.identifierCode).
bridg:Place.identifierCode
urn:AE:Receiver.jurisdiction
bridg:Place.identifierCode
urn:AE:Reporter.jurisdiction
bridg:Place.identifierCode
urn:CTR_Rr2:SUSAR_Reporting_to_EVCTM
bridg:Place.identifierCode
urn:CTR_Rr2:Country_granting_MA
bridg:Place.identifierCode
urn:CTR_Rr2:SUSAR_Reporting_to_NCAs
bridg:Place.identifierCode
urn:CTRPv1.0:RegulatoryAuthority.jurisdictionCode
bridg:Place.identifierCode
urn:CTRPv3.8:RegulatoryAuthority.countryCode
bridg:Place.identifierCode
urn:CTRv1.0:Place.code
in R_Product
bridg:Place.identifierCode
urn:ICSRr2:territory.code
bridg:Place.name
name
bridg:Place.name
false
bridg:Place.name
A non-unique textual identifier for the place
bridg:Place.name
"European Union" might be the name of the territory comprised by the EU member states.
bridg:Place.name
urn:CTRv1.0:Place.name
bridg:Place.name
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Manufacturing_site
in E_Place universal
bridg:Place.name
urn:ICSRr2:Place.name
in R_Product
bridg:Place.name
urn:ICSRr2:Territory.name
in IndividualCaseSafetyReport
bridg:Place.name
urn:ICSRr2:Place.name
bridg:Place.physicalAddress
physicalAddress
bridg:Place.physicalAddress
false
bridg:Place.physicalAddress
A representation of the location of the place.
bridg:Place.physicalAddress
The physicalAddress attribute is meant to provide sufficient information to allow someone to visit a place; it is not intended to provide geographic categorization, a postal address, or a simple name by which a country/state/city is referenced (for a simple name use Place.name).
bridg:Place.physicalAddress
urn:CTRv1.0:Place.physicalAddress
in E_Place universal
bridg:Place.physicalAddress
urn:ICSRr2:Place.addr
bridg:Place.physicalAddress
urn:caAERSv2.2:MedicalDevice.reprocessorAddress
bridg:Place.physicalAddress
urn:caAERSv2.2:MedicalDevice.manufacturerState
bridg:Place.physicalAddress
urn:caAERSv2.2:MedicalDevice.manufacturerCity
bridg:Place.typeCode
typeCode
bridg:Place.typeCode
false
bridg:Place.typeCode
A coded value specifying the kind of place.
bridg:Place.typeCode
emergency department
bridg:Place.typeCode
surgical suite
bridg:Place.typeCode
patient room
bridg:Place.typeCode
urn:AE:ServiceDeliveryLocation.locationTypeCode
bridg:Place.typeCode
urn:CTRv1.0:Place.typeCode
bridg:Place.typeCode
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Product_thawed_at_bedside
in IndividualCaseSafetyReport
bridg:Place.typeCode
urn:ICSRr2:Place.code
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
agentAdministrationCareSettingTypeCode
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
false
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
A coded value specifying the level of healthcare (care setting) required by the subject based on the nature of the procedure.
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
Some
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
but not all
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
agents given as inpatient
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
All agents given as inpatient
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
All agents given as outpatient
bridg:PlannedActivity.agentAdministrationCareSettingTypeCode
urn:HCTv1.0:CDE_2956638:Therapies.What_was_the_protocol_requirement_type:
bridg:PlannedActivity.blindedDescription
blindedDescription
bridg:PlannedActivity.blindedDescription
false
bridg:PlannedActivity.blindedDescription
The textual representation of the planned activity from the point of view of a blinded participant (study subject or study investigator).
bridg:PlannedActivity.blindedDescription
During the second treatment epoch of a study
bridg:PlannedActivity.blindedDescription
Arms A and B are still blinded and Arm C is no longer blinded. So
bridg:PlannedActivity.blindedDescription
Arm A and B must have identical blindedDescriptions.
bridg:PlannedActivity.blindedDescription
In a study with 3 arms
bridg:PlannedActivity.blindedDescription
Arm 1: standard vaccine given in three shots at 2 months
bridg:PlannedActivity.blindedDescription
5 months
bridg:PlannedActivity.blindedDescription
and 12 months of age; Arm 2: new vaccine given in three shots at 2 months
bridg:PlannedActivity.blindedDescription
5 months
bridg:PlannedActivity.blindedDescription
and 12 months of age; Arm 3: new vaccine given in two shots at 2 months and 5 months of age. Subjects assigned to the third arm are unblinded at some point during 5 months and 12 months. By the time of the Third Shot Epoch
bridg:PlannedActivity.blindedDescription
the "Arm 3/Third Shot" activity can be called by this
bridg:PlannedActivity.blindedDescription
its unblinded name. However
bridg:PlannedActivity.blindedDescription
the "Arm 1/Third Shot" and "Arm2/Third Shot" activities still need blinded names. Both these activities would have the blinded name (something like) "3-shot Arm/Third Shot".
bridg:PlannedActivity.blindedDescription
urn:C3PR:PlannedStudyCell.blindedDescription
bridg:PlannedActivity.blindedDescription
urn:CTRRr3:PlannedActivity.blindedDescription
bridg:PlannedActivity.blindedDescription
urn:CTRv1.0:PlannedActivity.blindedDescription
bridg:PlannedActivity.blindedDescription
urn:TDM:TrialCell.blindedDescription
bridg:PlannedActivity.description
description
bridg:PlannedActivity.description
false
bridg:PlannedActivity.description
The textual representation of the planned activity.
bridg:PlannedActivity.description
In a migraine study
bridg:PlannedActivity.description
the Wait activity may have a description of "Wait until first grade 2 or 3 migraine".
bridg:PlannedActivity.description
urn:C3PRv2.9:Arm.descriptionText
bridg:PlannedActivity.description
urn:CTRPv3.8:PlannedSubstanceAdministration.doseDescription
bridg:PlannedActivity.description
urn:CTRPv3.8:Activity.textDescription
bridg:PlannedActivity.description
urn:CTRRr3:PlannedActivity.description
bridg:PlannedActivity.description
urn:CTRRr3:PlannedIntervention.description
bridg:PlannedActivity.description
urn:CTRv1.0:PlannedActivity.description
bridg:PlannedActivity.description
urn:PSCv2.6:PlannedActivity.details
bridg:PlannedActivity.description
urn:SDTM_IGv3.1.1:TE.ELEMENT
bridg:PlannedActivity.description
urn:SDTM_IGv3.1.1:TA.ELEMENT
bridg:PlannedActivity.description
urn:TDM:StudyDesignElement.description
bridg:PlannedActivity.description
urn:caAERSv2.2:TreatmentAssignment.doseLevelOrder
bridg:PlannedActivity.duration
duration
bridg:PlannedActivity.duration
false
bridg:PlannedActivity.duration
The intended period of time for the planned activity as defined by the study.
bridg:PlannedActivity.duration
6 weeks may be the planned duration for a composite activity that represents the activities occurring during an epoch on arm A.
bridg:PlannedActivity.duration
urn:CTR_Rr2:Maximum_duration_of_treatment
bridg:PlannedActivity.duration
urn:CTRRr3:PlannedActivity.plannedDuration
bridg:PlannedActivity.duration
urn:CTRv1.0:DefinedActivity.duration
bridg:PlannedActivity.duration
urn:CTRv1.0:PlannedActivity.duration
bridg:PlannedActivity.duration
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component4/timePointEventDefinition.effectiveTime
bridg:PlannedActivity.duration
urn:LabViewer2.2:Activity.plannedTimeElapsed
bridg:PlannedActivity.duration
urn:LabViewer2.2:SpecimenCollection.plannedTimeElapsedDescription
bridg:PlannedActivity.duration
urn:LabViewer2.2:plannedTimeElapsedDescription
bridg:PlannedActivity.duration
urn:LabViewer2.2:SpecimenCollection.plannedTimeElapsed
bridg:PlannedActivity.duration
urn:PSC:Duration.quantity
bridg:PlannedActivity.duration
urn:PSC:Duration.units
bridg:PlannedActivity.duration
urn:PSCv2.6:Duration.units
bridg:PlannedActivity.duration
urn:PSCv2.6:StudySegment.cycleLength
bridg:PlannedActivity.duration
urn:PSCv2.6:Duration.quantity
bridg:PlannedActivity.duration
urn:SDTM_IGv3.1.1:TE.TEDUR
bridg:PlannedActivity.duration
urn:SDTM_IGv3.1.2:TE.TEDUR
bridg:PlannedActivity.interruptibleIndicator
interruptibleIndicator
bridg:PlannedActivity.interruptibleIndicator
false
bridg:PlannedActivity.interruptibleIndicator
Specifies whether the planned activity is interruptable by asynchronous events.
bridg:PlannedActivity.interruptibleIndicator
This may only be useful for PlannedSubjectActivityGroups or administrative activities.
bridg:PlannedActivity.interruptibleIndicator
urn:HL7SDr1:TimePointEventDefinition.interruptibleInd
bridg:PlannedActivity.name
name
bridg:PlannedActivity.name
false
bridg:PlannedActivity.name
A non-unique textual identifier for the planned activity.
bridg:PlannedActivity.name
urn:C3PR:PlannedStudyCell.name
bridg:PlannedActivity.name
urn:C3PRv2.9:PlannedNotification.eventName
bridg:PlannedActivity.name
urn:C3PRv2.9:Arm.name
bridg:PlannedActivity.name
urn:CDASHv1.1:PE.VISIT
bridg:PlannedActivity.name
urn:CDASHv1.1:EG.VISIT
bridg:PlannedActivity.name
urn:CDASHv1.1:VS.VISIT
bridg:PlannedActivity.name
urn:CDASHv1.1:LB.LBTPT
bridg:PlannedActivity.name
urn:CDASHv1.1:IE.VISIT
bridg:PlannedActivity.name
urn:CDASHv1.1:EG.EGTPT
bridg:PlannedActivity.name
urn:CDASHv1.1:EX.EXTPT
bridg:PlannedActivity.name
urn:CDASHv1.1:LB.VISIT
bridg:PlannedActivity.name
urn:CDASHv1.1:DA.VISIT
bridg:PlannedActivity.name
urn:CDASHv1.1:VS.VSTPT
bridg:PlannedActivity.name
urn:CTOM:StudyTimePoint.courseNumber
bridg:PlannedActivity.name
urn:CTOM:StudyTimePoint.visitName
bridg:PlannedActivity.name
urn:CTRPv1.0:PlannedObservation.name
bridg:PlannedActivity.name
urn:CTRPv1.0:PlannedActivity.name
bridg:PlannedActivity.name
urn:CTRPv1.0:SubstanceAdministration.name
bridg:PlannedActivity.name
urn:CTRPv3.8:Intervention.name
bridg:PlannedActivity.name
urn:CTRPv3.8:PlannedActivity.alternateName
bridg:PlannedActivity.name
urn:CTRPv3.8:PerformedActivity.name
bridg:PlannedActivity.name
urn:CTRPv3.8:PlannedEligibilityCriterion.criterionName
bridg:PlannedActivity.name
urn:CTRRr3:PlannedIntervention.name
bridg:PlannedActivity.name
urn:CTRv1.0:PlannedActivity.name
bridg:PlannedActivity.name
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component4/timePointEventDefinition.title
bridg:PlannedActivity.name
urn:PSC:Arm.name
bridg:PlannedActivity.name
urn:PSCv2.6:Period.name
bridg:PlannedActivity.name
urn:PSCv2.6:StudySegment.name
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:DA.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:SU.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:TA.ETCD
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:TE.ETCD
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:EG.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:EG.EGTPTNUM
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:LB.LBTPTNUM
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:TV.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:VS.VSTPTNUM
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:VS.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:LB.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:QS.QSTPTNUM
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:PE.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:QS.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:MH.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:SV.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.1:IE.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:MS.MSTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:DA.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:MS.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:FA.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:PC.PCTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:IE.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:MB.MBTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:QS.QSTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:EG.EGTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:PC.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:QS.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:PE.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:EG.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:MB.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:VS.VSTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:EX.EXTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:LB.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:TV.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:LB.LBTPT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:VS.VISIT
bridg:PlannedActivity.name
urn:SDTM_IGv3.1.2:SV.VISIT
bridg:PlannedActivity.name
urn:TDM:StudyDesignElement.name
bridg:PlannedActivity.name
urn:TDM:SubjectTrialContact.eventAlias
bridg:PlannedActivity.purpose
purpose
bridg:PlannedActivity.purpose
false
bridg:PlannedActivity.purpose
The reason for the planned activity.
bridg:PlannedActivity.purpose
treating a disease (treatment)
bridg:PlannedActivity.purpose
determining eligibility for a study (screening)
bridg:PlannedActivity.purpose
Per GForge Tracker item 31402, this attribute is redundant and we're deprecating it in favor of the existing Activity.reasonCode.
bridg:PlannedActivity.purpose
urn:CTRv1.0:PlannedActivity.purpose
New content
bridg:PlannedActivity.purpose
urn:TDMv2:
bridg:PlannedActivity.repeatDuration
repeatDuration
bridg:PlannedActivity.repeatDuration
true
bridg:PlannedActivity.repeatDuration
The period of time over which the planned activity is repeated.
bridg:PlannedActivity.repeatDuration
Derived from repeatQuantity and repeatFrequencyCode or repeatFrequencyRatio (constraint allows only one). In any given implementation, if quantity is not provided, duration may be provided instead, however the BRIDG team determined that quantity is considered more fundamental for a domain analysis model.
bridg:PlannedActivity.repeatDuration
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatDuration
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatDuration
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatDuration
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatDuration
urn:CTRv1.0:PlannedActivity.repeatDuration
bridg:PlannedActivity.repeatDuration
urn:TDM:CyclingRule
bridg:PlannedActivity.repeatFrequencyCode
repeatFrequencyCode
bridg:PlannedActivity.repeatFrequencyCode
false
bridg:PlannedActivity.repeatFrequencyCode
A coded value specifying the number of occurrences of a planned activity within a given time period.
bridg:PlannedActivity.repeatFrequencyCode
BID = Two times per day
bridg:PlannedActivity.repeatFrequencyCode
at unspecified times (does not necessarily imply that these are 12 hours apart)
bridg:PlannedActivity.repeatFrequencyCode
Q12H = Every twelve hours
bridg:PlannedActivity.repeatFrequencyCode
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyCode
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyCode
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyCode
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyCode
urn:CTRv1.0:PlannedActivity.repeatFrequencyCode
bridg:PlannedActivity.repeatFrequencyCode
urn:TDM:CyclingRule
bridg:PlannedActivity.repeatFrequencyRatio
repeatFrequencyRatio
bridg:PlannedActivity.repeatFrequencyRatio
false
bridg:PlannedActivity.repeatFrequencyRatio
A ratio representing the number of occurrences of a planned activity within a given time period.
bridg:PlannedActivity.repeatFrequencyRatio
Once per 12 hours
bridg:PlannedActivity.repeatFrequencyRatio
2 times per day
bridg:PlannedActivity.repeatFrequencyRatio
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyRatio
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyRatio
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyRatio
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatFrequencyRatio
urn:CTRv1.0:PlannedActivity.repeatFrequencyRatio
bridg:PlannedActivity.repeatFrequencyRatio
urn:TDM:CyclingRule
bridg:PlannedActivity.repeatQuantityRange
repeatQuantityRange
bridg:PlannedActivity.repeatQuantityRange
false
bridg:PlannedActivity.repeatQuantityRange
An integer falling within minimum and maximum bounds that specifies how many times the planned activity occurs.
bridg:PlannedActivity.repeatQuantityRange
If the frequency is more than once a day, this is still interpreted per time, e.g. BID for 5 days is 10 repeats.
bridg:PlannedActivity.repeatQuantityRange
urn:CTRPv1.0:PlannedActivity.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatQuantityRange
urn:CTRPv1.0:PlannedEligibilityCriterion.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatQuantityRange
urn:CTRPv1.0:PlannedObservation.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatQuantityRange
urn:CTRPv1.0:SubstanceAdministration.plannedRangeOfRepetitions
bridg:PlannedActivity.repeatQuantityRange
urn:PSC:Period.repetitions
bridg:PlannedActivity.repeatQuantityRange
urn:PSCv2.6:Period.repetitions
bridg:PlannedActivity.repeatQuantityRange
urn:TDM:CyclingRule
bridg:PlannedActivity.studyDayRange
studyDayRange
bridg:PlannedActivity.studyDayRange
true
bridg:PlannedActivity.studyDayRange
The relative timing for a planned activity expressed as the number of days offset from the study-defined reference activity (e.g., date of registration, start of treatment) for a particular subject, study subject or experimental unit.
bridg:PlannedActivity.studyDayRange
Day 1
bridg:PlannedActivity.studyDayRange
Days 10-20
bridg:PlannedActivity.studyDayRange
Visit Day
bridg:PlannedActivity.studyDayRange
Derived from all the pauseQuantity values of the composite activity structures that this activity is a part of minus the offset of the reference activity.
The study-defined reference activity can be different from study to study. The study day for a date after this reference activity is a positive integer calculated as the difference in the two dates + 1. The study day for dates before the reference activity is a negative integer calculated as the difference between the two dates. Note that this means there is no "Day 0."
bridg:PlannedActivity.studyDayRange
urn:CTRv1.0:PlannedActivity.studyDayRange
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:TV.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:QS.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:PC.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:FA.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:SV.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:EG.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:DA.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:PE.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:MS.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:VS.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:IE.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:MB.VISITDY
bridg:PlannedActivity.studyDayRange
urn:SDTM_IGv3.1.2:LB.VISITDY
bridg:PlannedCompositionRelationship.joinCode
joinCode
bridg:PlannedCompositionRelationship.joinCode
false
bridg:PlannedCompositionRelationship.joinCode
A coded value specifying whether, and how, a specific activity in a set of parallel activities should come together before subsequent activities can begin.
bridg:PlannedCompositionRelationship.joinCode
Wait for this activity to complete before the subsequent activity; Terminate this activity as soon as all parallel "wait" activities are completed (and if this activity hasn't started yet
bridg:PlannedCompositionRelationship.joinCode
don't start it at all); Continue this activity after all "wait" activities complete
bridg:PlannedCompositionRelationship.joinCode
but don't wait for it to complete before beginning subsequent activities.
bridg:PlannedCompositionRelationship.joinCode
urn:CTRv1.0:PlannedCompositionRelationship.joinCode
bridg:PlannedCompositionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:PlannedCompositionRelationship.pauseQuantityRange
false
bridg:PlannedCompositionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:PlannedCompositionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:PlannedCompositionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:PlannedCompositionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:HL7SD:PlannedStudy.Component2.pauseQuantity
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.day
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.units
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.startDay
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:PSCv2.6:PlannedActivity.day
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:PSCv2.6:Period.startDay
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.1:EX.EXELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:PC.PCELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:EX.EXELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:MB.MBELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:LB.LBELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:QS.QSELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:MS.MSELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:EG.EGELTM
bridg:PlannedCompositionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:VS.VSELTM
bridg:PlannedCompositionRelationship.sequenceNumber
sequenceNumber
bridg:PlannedCompositionRelationship.sequenceNumber
false
bridg:PlannedCompositionRelationship.sequenceNumber
An integer specifying the relative sequential or temporal ordering of this relationship among other similar relationships having the same source.
bridg:PlannedCompositionRelationship.sequenceNumber
In a course of treatment (a composite activity) that is composed of a chemotherapy activity and a radiotherapy activity, the sequence number indicates which component activity precedes the other.
bridg:PlannedCompositionRelationship.sequenceNumber
urn:C3PR:EligibilityCriterion.questionNumber
bridg:PlannedCompositionRelationship.sequenceNumber
urn:C3PRv2.9:EligibilityCriteria.questionNumber
bridg:PlannedCompositionRelationship.sequenceNumber
urn:C3PRv2.9:StratificationCriterion.questionNumber
bridg:PlannedCompositionRelationship.sequenceNumber
urn:CTOM:ActivityRelationship.sequenceNumber
bridg:PlannedCompositionRelationship.sequenceNumber
urn:CTRv1.0:PlannedCompositionRelationship.sequenceNumber
bridg:PlannedCompositionRelationship.sequenceNumber
urn:HL7SD:PlannedStudy.Component2.sequenceNumber
bridg:PlannedCompositionRelationship.sequenceNumber
urn:PSCv2.6:PlannedActivity.weight
bridg:PlannedContingentOnRelationship.checkpointCode
checkpointCode
bridg:PlannedContingentOnRelationship.checkpointCode
false
bridg:PlannedContingentOnRelationship.checkpointCode
bridg:PlannedContingentOnRelationship.checkpointCode
The checkpointCode specifies when the precondition is to be checked; it is analogous to the various conditional statements and loop constructs in programming languages "while-do" vs. "do-while" or "repeat-until" vs. "loop-exit."
bridg:PlannedContingentOnRelationship.checkpointCode
urn:HL7SDr1:Precondition3.checkpointCode
bridg:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
completionRequiredBeforeStartingIndicator
bridg:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
false
bridg:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
Specifies whether the target activity must have completed prior to starting the source activity.
bridg:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
This attribute may only be used if the target is an activity, not if the target is an observation result or a criterion group.
bridg:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
urn:CTRv1.0:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
bridg:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
urn:TDMv2:PlannedContingentOnRelationship.completionRequiredBeforeStartingIndicator
bridg:PlannedContingentOnRelationship.pauseQuantityRange
pauseQuantityRange
bridg:PlannedContingentOnRelationship.pauseQuantityRange
false
bridg:PlannedContingentOnRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:PlannedContingentOnRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:PlannedContingentOnRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:PlannedContingentOnRelationship.pauseQuantityRange
For the more complex examples of doing activity A 5 minutes after the start of B or 5 minutes after the end of B
bridg:PlannedContingentOnRelationship.pauseQuantityRange
use pauseQuantity in combination with completionRequiredBeforeStartingIndicator where the pauseQuantity in both cases would be 5 minutes and "after the start of" would be completionRequiredBeforeStartingIndicator = "false" and "after the end of" = "true".
bridg:PlannedContingentOnRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.startDay
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.units
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.day
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.1:EX.EXELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:EG.EGELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:PC.PCELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:MS.MSELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:MB.MBELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:EX.EXELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:LB.LBELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:QS.QSELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.2:VS.VSELTM
bridg:PlannedContingentOnRelationship.pauseQuantityRange
urn:caAERSv2.2:PlannedNotification.interval
bridg:PlannedContingentOnRelationship.priorityNumber
priorityNumber
bridg:PlannedContingentOnRelationship.priorityNumber
false
bridg:PlannedContingentOnRelationship.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:PlannedContingentOnRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:PlannedContingentOnRelationship.priorityNumber
urn:HL7SDr1:Precondition3.priorityNumber
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
joinCode
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
false
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
A coded value specifying whether, and how, a specific activity in a set of parallel activities should come together before subsequent activities can begin.
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
Wait for this activity to complete before the subsequent activity; Terminate this activity as soon as all parallel "wait" activities are completed (and if this activity hasn't started yet
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
don't start it at all); Continue this activity after all "wait" activities complete
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
but don't wait for it to complete before beginning subsequent activities.
bridg:PlannedCriterionGroupCompositionRelationship.joinCode
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship.joinCode
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
false
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.units
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.day
bridg:PlannedCriterionGroupCompositionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.startDay
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
sequenceNumber
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
false
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
An integer specifying the relative sequential or temporal ordering of this relationship among other similar relationships having the same source.
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
In a criterion group that is composed of a substance administration activity and a lab test activity
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
the sequence number indicates which activity precedes the other.
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
urn:CTOM:ActivityRelationship.sequenceNumber
bridg:PlannedCriterionGroupCompositionRelationship.sequenceNumber
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship.sequenceNumber
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
false
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.startDay
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.day
bridg:PlannedCriterionGroupOptionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.units
bridg:PlannedCriterionGroupOptionRelationship.priorityNumber
priorityNumber
bridg:PlannedCriterionGroupOptionRelationship.priorityNumber
false
bridg:PlannedCriterionGroupOptionRelationship.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:PlannedCriterionGroupOptionRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:PlannedCriterionGroupOptionRelationship.priorityNumber
urn:CTRv1.0:PlannedCriterionGroupOptionRelationship.priorityNumber
bridg:PlannedCriterionGroupOptionRelationship.priorityNumber
urn:TDM:AbstractRule.isExclusive
bridg:PlannedNotification.studyAccrualThresholdPercent
studyAccrualThresholdPercent
bridg:PlannedNotification.studyAccrualThresholdPercent
false
bridg:PlannedNotification.studyAccrualThresholdPercent
An integer specifying a percentage of target accrual for a study, which when reached triggers a notification.
bridg:PlannedNotification.studyAccrualThresholdPercent
75% or 90% of the target accrual number.
bridg:PlannedNotification.studyAccrualThresholdPercent
urn:C3PRv2.9:PlannedNotification.studyThreshold
bridg:PlannedNotification.studySiteAccrualThresholdPercent
studySiteAccrualThresholdPercent
bridg:PlannedNotification.studySiteAccrualThresholdPercent
false
bridg:PlannedNotification.studySiteAccrualThresholdPercent
An integer specifying a percentage of target accrual at a particular study site, which when reached triggers a notification.
bridg:PlannedNotification.studySiteAccrualThresholdPercent
75% or 90% of the target accrual number.
bridg:PlannedNotification.studySiteAccrualThresholdPercent
urn:C3PRv2.9:PlannedNotification.studySiteThreshold
bridg:PlannedOptionRelationship.pauseQuantityRange
pauseQuantityRange
bridg:PlannedOptionRelationship.pauseQuantityRange
false
bridg:PlannedOptionRelationship.pauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time between when an activity is ready for execution and the actual beginning of the execution.
bridg:PlannedOptionRelationship.pauseQuantityRange
Take a blood sample 15 minutes after administration of study drug or measure blood glucose 2 hours after each meal
bridg:PlannedOptionRelationship.pauseQuantityRange
the pauseQuantity would be 15 minutes and 2 hours respectively.
bridg:PlannedOptionRelationship.pauseQuantityRange
The pauseQuantity defines the amount of time between two points in time: (1) the point when all preceding steps (in sequence) and preconditions of an activity have been completed, and (2) the actual start of the activity. The completion of all pre-conditions and preceding steps (based on sequence number) indicates that an activity is "ready for execution" according to the definition above. The pauseQuantity counter or timeclock starts then, and when the full amount of time is reached, the activity begins. A pauseQuantity with a negative value means that the activity starts some amount of time prior to the estimated time that the activity is "ready for execution", i.e. prior to the estimated time that the pre-conditions and preceding steps will be completed.
bridg:PlannedOptionRelationship.pauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:PlannedOptionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.day
bridg:PlannedOptionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.startDay
bridg:PlannedOptionRelationship.pauseQuantityRange
urn:PSC:PlannedEvent.units
bridg:PlannedOptionRelationship.pauseQuantityRange
urn:SDTM_IGv3.1.1:EX.EXELTM
bridg:PlannedOptionRelationship.priorityNumber
priorityNumber
bridg:PlannedOptionRelationship.priorityNumber
false
bridg:PlannedOptionRelationship.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:PlannedOptionRelationship.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:PlannedOptionRelationship.priorityNumber
urn:CTRv1.0:PlannedOptionRelationship.priorityNumber
bridg:PlannedOptionRelationship.priorityNumber
urn:TDM:AbstractRule.isExclusive
bridg:PlannedRepeatActivityUntilRule.cessationPauseQuantityRange
cessationPauseQuantityRange
bridg:PlannedRepeatActivityUntilRule.cessationPauseQuantityRange
false
bridg:PlannedRepeatActivityUntilRule.cessationPauseQuantityRange
A quantity of time falling within minimum and maximum bounds that specifies the elapsed time after the observed result occurs and before the cessation of repeating the activity.
bridg:PlannedRepeatActivityUntilRule.cessationPauseQuantityRange
Stop 20 days after the observed event occurs.
bridg:PlannedRepeatActivityUntilRule.cessationPauseQuantityRange
urn:Lab:Activity.plannedTimeElapsed
bridg:PlannedRepeatActivityUntilRule.checkpointCode
checkpointCode
bridg:PlannedRepeatActivityUntilRule.checkpointCode
false
bridg:PlannedRepeatActivityUntilRule.checkpointCode
bridg:PlannedRepeatActivityUntilRule.checkpointCode
The checkpointCode specifies when the precondition is to be checked; it is analogous to the various conditional statements and loop constructs in programming languages "while-do" vs. "do-while" or "repeat-until" vs. "loop-exit."
bridg:PlannedRepeatActivityUntilRule.checkpointCode
urn:HL7SDr1:Precondition3.checkpointCode
bridg:PlannedRepeatActivityUntilRule.priorityNumber
priorityNumber
bridg:PlannedRepeatActivityUntilRule.priorityNumber
false
bridg:PlannedRepeatActivityUntilRule.priorityNumber
A number specifying the relative preference for considering this relationship before other like-typed relationships having the same source activity.
bridg:PlannedRepeatActivityUntilRule.priorityNumber
Relationships with lower priorityNumber values are considered before and above those with higher values.
The ordering may be a total ordering, in which all priority number are unique, or a partial ordering, in which the same priority may be assigned to more than one relationship. Decimal numbers may be used to insert values between existing priority numbers.
For multiple criteria, this specifies which criteria are considered before others.
Among alternatives or options that are being chosen by humans, the priorityNumber specifies preference.
bridg:PlannedRepeatActivityUntilRule.priorityNumber
urn:HL7SDr1:Precondition3.priorityNumber
bridg:PlannedStudySite.duration
duration
bridg:PlannedStudySite.duration
false
bridg:PlannedStudySite.duration
The intended period of time for the planned study site's participation in the study.
bridg:PlannedStudySite.duration
urn:BRIDGSCC:Model_Integrity_-_Study_Versioning
bridg:PlannedStudySite.duration
urn:CTRv1.0:PlannedStudySite.duration
bridg:PlannedStudySite.leadIndicator
leadIndicator
bridg:PlannedStudySite.leadIndicator
false
bridg:PlannedStudySite.leadIndicator
Specifies whether this is the principal administrative organization intended to be responsible for the study.
bridg:PlannedStudySite.leadIndicator
Exception: A multi-site study with no single assigned coordination center; in this case, every participating organization can be named as lead organization.
bridg:PlannedStudySite.leadIndicator
urn:C3PR:StudySite.roleCode
bridg:PlannedStudySite.leadIndicator
urn:CTOM:StudySite.roleCode
bridg:PlannedStudySite.leadIndicator
urn:CTRv1.0:PlannedStudySite.leadIndicator
bridg:PlannedStudySubject.quantityRange
quantityRange
bridg:PlannedStudySubject.quantityRange
false
bridg:PlannedStudySubject.quantityRange
An integer falling within minimum and maximum bounds that specifies how many of a particular type of subject are planned to be included in the study.
bridg:PlannedStudySubject.quantityRange
urn:FDA_HL7_SD_SD_DSTU2012:personKind.quantity
bridg:PlannedSubjectActivityGroup.sequenceNumber
sequenceNumber
bridg:PlannedSubjectActivityGroup.sequenceNumber
true
bridg:PlannedSubjectActivityGroup.sequenceNumber
An integer specifying the order of a visit within a study.
bridg:PlannedSubjectActivityGroup.sequenceNumber
Visit Number
bridg:PlannedSubjectActivityGroup.sequenceNumber
Derived from the sequence number that orders this activity group within a larger activity group:
PlannedSubjectActivityGroup [visit, timepoint or other kind of group] > PlannedCompositionRelationship.sequenceNumber > PlannedSubjectActivityGroup [set of planned visits for the study or some other larger activity group]
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CDASHv1.1:IE.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CDASHv1.1:LB.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CDASHv1.1:VS.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CDASHv1.1:EG.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CDASHv1.1:DA.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CDASHv1.1:PE.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:CTRv1.0:PlannedSubjectActivityGroup.sequenceNumber
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:MS.MSTPTNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:MB.MBTPTNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:PC.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:MS.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:EG.EGTPTNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:IE.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:TV.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:PE.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:SV.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:DA.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:MB.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:FA.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:LB.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:PC.PCTPTNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:QS.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:EG.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:VS.VISITNUM
bridg:PlannedSubjectActivityGroup.sequenceNumber
urn:SDTM_IGv3.1.2:EX.EXTPTNUM
bridg:PlannedSubjectActivityGroup.targetAccrualNumberRange
targetAccrualNumberRange
bridg:PlannedSubjectActivityGroup.targetAccrualNumberRange
false
bridg:PlannedSubjectActivityGroup.targetAccrualNumberRange
An integer falling within minimum and maximum bounds that specifies how many subjects are to be accrued for the planned subject activity group.
bridg:PlannedSubjectActivityGroup.targetAccrualNumberRange
urn:BRIDGv2.2:PlannedStudyCell.targetAccrualNumber
bridg:PlannedSubjectActivityGroup.targetAccrualNumberRange
urn:C3PRv2.9:Arm.targetAccrualNumber
bridg:PlannedSubjectActivityGroup.targetAccrualNumberRange
urn:CTRv1.0:PlannedActivity.targetAccrualNumberRange
bridg:ProcessedProduct.identifier
identifier
bridg:ProcessedProduct.identifier
false
bridg:ProcessedProduct.identifier
A unique symbol used by the processor to establish identify of a particular product type or line.
bridg:ProcessedProduct.identifier
catalog number
bridg:ProcessedProduct.identifier
There are multiple ways in which an identifier can be associated to a product; inherited from MaterialIdentifier.identifier, the association to ProcessedProduct.identifier, and the association to ProductRelationship.identifier. If there is no context associated with the identifier, then MaterialIdentifier.identifier should be used. However, if the identifier for a product would be different in a different context, one of the other identifiers should be used. If a kind of product is produced by different processors, and each processor assigns the product a different identifier, then ProcessedProduct.identifier should be used. If the product is used in multiple assemblies, and in each assembly it would be assigned a different identifier, then ProductRelationship.identifier should be used.
bridg:ProcessedProduct.identifier
urn:CTRv1.0:ProcessedProduct.identifier
in R_Product
bridg:ProcessedProduct.identifier
urn:ICSRr2:ManufacturedProduct2.id
bridg:Product.classCode
classCode
bridg:Product.classCode
false
bridg:Product.classCode
A coded value specifying a group of products that are homogeneous or generally considered as substitutes for each other.
bridg:Product.classCode
stents
bridg:Product.classCode
breakfast cereals
bridg:Product.classCode
cox-2 inhibitors
bridg:Product.classCode
The class is considered as narrow or broad depending on how substitutable the various products are.
bridg:Product.classCode
urn:AE:ProductClass.typeCode
bridg:Product.classCode
urn:AE:ProductClass.name
bridg:Product.classCode
urn:AE:ProductClass
bridg:Product.classCode
urn:CDASHv1.1:CM.CMCLASCD
bridg:Product.classCode
urn:CDASHv1.1:CM.CMCLAS
bridg:Product.classCode
urn:CTR_Rr2:Tissue_Engineered_MP
bridg:Product.classCode
urn:CTR_Rr2:IMP_ATC_Code
bridg:Product.classCode
urn:CTR_Rr2:Plasma_derived_MP
Genetically Modified Organism MP
bridg:Product.classCode
urn:CTR_Rr2:GMO
bridg:Product.classCode
urn:CTR_Rr2:CAT_Classification
bridg:Product.classCode
urn:CTR_Rr2:Recombinant_MP
bridg:Product.classCode
urn:CTR_Rr2:Gene_therapy_MP
Chemical Abstract Service number
bridg:Product.classCode
urn:CTR_Rr2:AS_CAS
bridg:Product.classCode
urn:CTR_Rr2:Extractive_MP
bridg:Product.classCode
urn:CTR_Rr2:Immunological_MP
bridg:Product.classCode
urn:CTR_Rr2:Somatic_cell_therapy_MP
bridg:Product.classCode
urn:CTR_Rr2:Radiopharmaceutical_MP
bridg:Product.classCode
urn:CTR_Rr2:Advanced_Therapy_MP
bridg:Product.classCode
urn:CTR_Rr2:Combination_ATIMP
committee for Advanced therapies Classification issued
bridg:Product.classCode
urn:CTR_Rr2:CAT
bridg:Product.classCode
urn:CTRPv1.0:Cosmetic.classCode
bridg:Product.classCode
urn:CTRPv1.0:Biologic.classCode
bridg:Product.classCode
urn:CTRPv1.0:FoodProduct.classCode
bridg:Product.classCode
urn:CTRPv1.0:Device.classCode
bridg:Product.classCode
urn:CTRPv1.0:Drug.classCode
bridg:Product.classCode
urn:CTRPv1.0:Product.classCode
bridg:Product.classCode
urn:CTRRr3:Product.classCode
bridg:Product.classCode
urn:CTRv1.0:Product.classCode
bridg:Product.classCode
urn:FDA_HL7_SD_SD_DSTU2012:manufacturedProduct.classCode
bridg:Product.classCode
urn:FDA_HL7_SD_SD_DSTU2012:ingredient.classCode
bridg:Product.classCode
urn:HL7SD:Product.classCode
bridg:Product.classCode
urn:SDTM_IGv3.1.1:SU.SUCLASCD
bridg:Product.classCode
urn:SDTM_IGv3.1.1:CM.CMCLASCD
bridg:Product.classCode
urn:SDTM_IGv3.1.1:SU.SUCLAS
bridg:Product.classCode
urn:SDTM_IGv3.1.1:CM.CMCLAS
bridg:Product.classCode
urn:SDTM_IGv3.1.2:SU.SUCLAS
bridg:Product.classCode
urn:SDTM_IGv3.1.2:CM.CMCLASCD
bridg:Product.classCode
urn:SDTM_IGv3.1.2:CM.CMCLAS
bridg:Product.classCode
urn:SDTM_IGv3.1.2:SU.SUCLASCD
bridg:Product.codeModifiedText
codeModifiedText
bridg:Product.codeModifiedText
false
bridg:Product.codeModifiedText
A character string that is a revision of the original text of the product to enable the coding of the text.
bridg:Product.codeModifiedText
If the original text is "aspriin"
bridg:Product.codeModifiedText
the CodeModifiedText could be set to "aspirin"
bridg:Product.codeModifiedText
so that the text can be successfully coded.
bridg:Product.codeModifiedText
In the context of BRIDG, text modification occurs a single time for a given instance of originalText.
bridg:Product.codeModifiedText
urn:CTRv1.0:Product.codeModifiedText
bridg:Product.codeModifiedText
urn:SDTM_IGv3.1.1:SU.SUMODIFY
bridg:Product.codeModifiedText
urn:SDTM_IGv3.1.1:CM.CMMODIFY
bridg:Product.codeModifiedText
urn:SDTM_IGv3.1.2:SU.SUMODIFY
bridg:Product.codeModifiedText
urn:SDTM_IGv3.1.2:CM.CMMODIFY
bridg:Product.expirationDate
expirationDate
bridg:Product.expirationDate
false
bridg:Product.expirationDate
The date (and time), assigned by the manufacturer, on which the product should not be used.
bridg:Product.expirationDate
urn:AE:Product.expirationDate
bridg:Product.expirationDate
urn:CTOM:AgentOccurrence.expirationDate
bridg:Product.expirationDate
urn:CTRPv1.0:Product.expirationDate
bridg:Product.expirationDate
urn:CTRPv1.0:Cosmetic.expirationDate
bridg:Product.expirationDate
urn:CTRPv1.0:Biologic.expirationDate
bridg:Product.expirationDate
urn:CTRPv1.0:Device.expirationDate
bridg:Product.expirationDate
urn:CTRPv1.0:FoodProduct.expirationDate
bridg:Product.expirationDate
urn:CTRPv1.0:Drug.expirationDate
bridg:Product.expirationDate
urn:CTRv1.0:Product.expirationDate
in R_Product
bridg:Product.expirationDate
urn:ICSRr2:DeviceInstance.expirationTime
in R_Product
bridg:Product.expirationDate
urn:ICSRr2:Product.expirationTime
in R_Product
bridg:Product.expirationDate
urn:ICSRr2:ProductInstance.expirationTime
bridg:Product.lotNumberText
lotNumberText
bridg:Product.lotNumberText
false
bridg:Product.lotNumberText
An alphanumeric string used to identify a particular batch of the product.
bridg:Product.lotNumberText
urn:AE:Package.lotNumber
bridg:Product.lotNumberText
urn:AE:Product.lotNumber
bridg:Product.lotNumberText
urn:CDASHv1.1:EX.EXLOT
bridg:Product.lotNumberText
urn:CTOM:AgentOccurrence.lotNumber
bridg:Product.lotNumberText
urn:CTRPv1.0:Drug.lotNumberText
bridg:Product.lotNumberText
urn:CTRPv1.0:Cosmetic.lotNumberText
bridg:Product.lotNumberText
urn:CTRPv1.0:FoodProduct.lotNumberText
bridg:Product.lotNumberText
urn:CTRPv1.0:Biologic.lotNumberText
bridg:Product.lotNumberText
urn:CTRv1.0:Product.lotNumberText
in R_Product
bridg:Product.lotNumberText
urn:ICSRr2:ProductInstance.lotNumberText
in R_Product
bridg:Product.lotNumberText
urn:ICSRr2:DeviceInstance.lotNumberText
in R_Product
bridg:Product.lotNumberText
urn:ICSRr2:Container.lotNumberText
bridg:Product.lotNumberText
urn:NCI_CRF_Standard:CDE_62592v3.0:_Agent_Lot_Identifier_Number
bridg:Product.lotNumberText
urn:SDTM_IGv3.1.1:EX.EXLOT
bridg:Product.lotNumberText
urn:SDTM_IGv3.1.2:EX.EXLOT
bridg:Product.lotNumberText
urn:caAERSv2.2:CourseAgent.lotNumber
bridg:Product.lotNumberText
urn:caAERSv2.2:MedicalDevice.lotNumber
bridg:Product.pre1938Indicator
pre1938Indicator
bridg:Product.pre1938Indicator
false
bridg:Product.pre1938Indicator
Specifies whether the product qualifies under the 1938 Grandfather Clause, contained in section 20l(p)(l) of the U.S. Federal Food, Drug and Cosmetic Act.
bridg:Product.pre1938Indicator
urn:AE:Product.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRPv1.0:Biologic.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRPv1.0:FoodProduct.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRPv1.0:Drug.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRPv1.0:Device.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRPv1.0:Cosmetic.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRPv1.0:Product.pre1938Indicator
bridg:Product.pre1938Indicator
urn:CTRv1.0:Product.pre1938Indicator
bridg:Product.typeCode
typeCode
bridg:Product.typeCode
false
bridg:Product.typeCode
A coded value specifying the kind of product.
bridg:Product.typeCode
veterinary medicine
bridg:Product.typeCode
diagnostic device
bridg:Product.typeCode
All members of a type share similar functions and general characteristics, especially the purpose for which they are used.
bridg:Product.typeCode
urn:AE:Package.typeCode
bridg:Product.typeCode
urn:AE:Product.typeCode
bridg:Product.typeCode
urn:AE:Component.typeCode
bridg:Product.typeCode
urn:AE:Ingredient.typeCode
bridg:Product.typeCode
urn:CTR_Rr2:Contains_Bio-materials
bridg:Product.typeCode
urn:CTR_Rr2:Contains_Scaffolds
bridg:Product.typeCode
urn:CTR_Rr2:Device_implantable
bridg:Product.typeCode
urn:CTR_Rr2:Herbal_MP
bridg:Product.typeCode
urn:CTR_Rr2:Device_Other
bridg:Product.typeCode
urn:CTR_Rr2:Contains_Matrices
bridg:Product.typeCode
urn:CTR_Rr2:Contains_medical_device
bridg:Product.typeCode
urn:CTR_Rr2:Other_MP
bridg:Product.typeCode
urn:CTR_Rr2:Homeopathic_MP
bridg:Product.typeCode
urn:CTR_Rr2:Other_MP_Specification
bridg:Product.typeCode
urn:CTRPv1.0:Cosmetic.typeCode
bridg:Product.typeCode
urn:CTRPv1.0:Drug.typeCode
bridg:Product.typeCode
urn:CTRPv1.0:Product.typeCode
bridg:Product.typeCode
urn:CTRPv1.0:FoodProduct.typeCode
bridg:Product.typeCode
urn:CTRPv1.0:Device.typeCode
bridg:Product.typeCode
urn:CTRPv1.0:Biologic.typeCode
bridg:Product.typeCode
urn:CTRPv3.8:PlannedSubstanceAdministration.radiationMachineType
bridg:Product.typeCode
urn:CTRPv3.8:Intervention.typeCode
bridg:Product.typeCode
urn:CTRRr3:Product.typeCode
bridg:Product.typeCode
urn:CTRv1.0:Product.typeCode
bridg:Product.typeCode
urn:HCTv1.0:CDE_2741552:Preparative_Regimen.What_type_of_radiolabeled_monoclonal_antibody_was_used_as_a_preparative_regimen?
bridg:Product.typeCode
urn:HCTv1.0:CDE_2705055:Lab_Results.Please_specify_the_person_for_whom_this_typing_is_being_done:
bridg:Product.typeCode
urn:HCTv1.0:CDE_2730912:Cell_Source.What_type_of_hematopoietic_stem_cell_transplant_was_used?
bridg:Product.typeCode
urn:HCTv1.0:CDE_2693219:Lab_Results.Who_is_being_tested_for_IDMs?
MAb?
bridg:Product.typeCode
urn:HCTv1.0:CDE_2741209:Preparative_Regimen.What_was_the_type_of_preparative_regimen_monoclonal_antibody
bridg:Product.typeCode
urn:HCTv1.0:CDE_2746489:Techniques.Specify_other_antibody.
bridg:Product.typeCode
urn:HCTv1.0:CDE_2527917:Cell_Source.Specify_the_other_hematopoietic_stem_cell_transplant_type:
bridg:Product.typeCode
urn:HCTv1.0:CDE_2750847:Preparative_Regimen.What_was_the_type_of_anthracycline_preparative_regimen?
bridg:Product.typeCode
urn:HL7SD:Product.code
in R_Product
bridg:Product.typeCode
urn:ICSRr2:Substance.code
in R_Product
bridg:Product.typeCode
urn:ICSRr2:Container.code
in R_Product
bridg:Product.typeCode
urn:ICSRr2:Product.code
in R_Product
bridg:Product.typeCode
urn:ICSRr2:PackagedProduct.code
bridg:Product.typeCode
urn:caAERSv2.2:MedicalDevice.deviceType
bridg:ProductGroup.actualIndicator
actualIndicator
bridg:ProductGroup.actualIndicator
false
bridg:ProductGroup.actualIndicator
Specifies whether the product group is a particular instance (actual) vs. universal kind.
bridg:ProductGroup.actualIndicator
To indicate a particular ProductGroup
bridg:ProductGroup.actualIndicator
actualIndicator = "true". To indicate a kind of ProductGroup
bridg:ProductGroup.actualIndicator
actualIndicator = "false".
choice box.determinerCode
bridg:ProductGroup.actualIndicator
urn:HL7SD:ExperimentalUnit_ExperimentalUnit2
bridg:ProductGroup.identifier
identifier
bridg:ProductGroup.identifier
false
bridg:ProductGroup.identifier
A unique symbol that establishes identity of the product group.
bridg:ProductGroup.identifier
urn:HL7SD:GroupKind.id
bridg:ProductGroup.quantity
quantity
bridg:ProductGroup.quantity
false
bridg:ProductGroup.quantity
The number of members in a product group.
bridg:ProductGroup.quantity
10 pills
bridg:ProductGroup.quantity
5 pace makers
bridg:ProductGroup.quantity
urn:HL7SD:GroupKind.quantity
bridg:ProductRelationship.activeIngredientIndicator
activeIngredientIndicator
bridg:ProductRelationship.activeIngredientIndicator
false
bridg:ProductRelationship.activeIngredientIndicator
Specifies whether the ingredient is an active ingredient.
bridg:ProductRelationship.activeIngredientIndicator
urn:AE:Ingredient.activeIngredientIndicator
bridg:ProductRelationship.activeIngredientIndicator
urn:CTR_Rr2:Chemical_origin_AS
bridg:ProductRelationship.activeIngredientIndicator
urn:CTR_Rr2:Biological_origin_AS
bridg:ProductRelationship.activeIngredientIndicator
urn:CTRPv1.0:FoodProduct.activeIngredientIndicator
bridg:ProductRelationship.activeIngredientIndicator
urn:CTRPv1.0:Cosmetic.activeIngredientIndicator
bridg:ProductRelationship.activeIngredientIndicator
urn:CTRPv1.0:Drug.activeIngredientIndicator
bridg:ProductRelationship.activeIngredientIndicator
urn:CTRRr3:ProductPart.activeIngredientIndicator
bridg:ProductRelationship.activeIngredientIndicator
urn:CTRv1.0:ProductRelationship.activeIngredientIndicator
bridg:ProductRelationship.confidentialityCode
confidentialityCode
bridg:ProductRelationship.confidentialityCode
false
bridg:ProductRelationship.confidentialityCode
A coded value specifying the privacy requirements for information about this relationship.
bridg:ProductRelationship.confidentialityCode
A manufacturer considers an ingredient in a product to be a trade secret.
bridg:ProductRelationship.confidentialityCode
urn:CTRv1.0:ProductRelationship.confidentialityCode
in R_Product
bridg:ProductRelationship.confidentialityCode
urn:ICSRr2:Ingredient.confidentialityCode
bridg:ProductRelationship.effectiveDateRange
effectiveDateRange
bridg:ProductRelationship.effectiveDateRange
false
bridg:ProductRelationship.effectiveDateRange
The date (and time) span for when the product relationship is active.
bridg:ProductRelationship.effectiveDateRange
urn:CTRv1.0:ProductRelationship.effectiveDateRange
in R_Product
bridg:ProductRelationship.effectiveDateRange
urn:ICSRr2:Ingredient.effectiveTime
bridg:ProductRelationship.identifier
identifier
bridg:ProductRelationship.identifier
false
bridg:ProductRelationship.identifier
A unique symbol that establishes identity of the product within the context of another product.
bridg:ProductRelationship.identifier
There are multiple ways in which an identifier can be associated to a product; inherited from MaterialIdentifier.identifier, the association to ProcessedProduct.identifier, and the association to ProductRelationship.identifier. If there is no context associated with the identifier, then MaterialIdentifier.identifier should be used. However, if the identifier for a product would be different in different context, one of the other identifiers should be used. If a kind of product is produced by different processors, and each processor assigns the product a different identifier, then ProcessedProduct.identifier should be used. If the product is used in multiple assemblies, and in each assembly it would be assigned a different identifier, then ProductRelationship.identifier should be used.
bridg:ProductRelationship.identifier
urn:CTRv1.0:ProductRelationship.identifier
in R_Product
bridg:ProductRelationship.identifier
urn:ICSRr2:Part.id
in R_Product
bridg:ProductRelationship.identifier
urn:ICSRr2:Ingredient.id
bridg:ProductRelationship.quantity
quantity
bridg:ProductRelationship.quantity
false
bridg:ProductRelationship.quantity
An indication of the amount of one product contained in another product.
bridg:ProductRelationship.quantity
50 mg per tablet
bridg:ProductRelationship.quantity
300 ml / liter
bridg:ProductRelationship.quantity
urn:AE:Ingredient.strength
bridg:ProductRelationship.quantity
urn:CTRPv1.0:Drug.strength
bridg:ProductRelationship.quantity
urn:CTRPv1.0:FoodProduct.strength
bridg:ProductRelationship.quantity
urn:CTRPv1.0:Biologic.strength
bridg:ProductRelationship.quantity
urn:CTRPv1.0:Cosmetic.strength
bridg:ProductRelationship.quantity
urn:CTRRr3:ProductPart.strength
bridg:ProductRelationship.quantity
urn:CTRv1.0:ProductRelationship.quantity
bridg:ProductRelationship.quantity
urn:FDA_HL7_SD_SD_DSTU2012:ingredient.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:Content.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:Content1.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:Container.capacityQuantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:Ingredient1.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:ProductInstance.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:InstanceOfKind.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:DeviceInstance.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:Ingredient.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:part.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:Content2.quantity
in R_Product
bridg:ProductRelationship.quantity
urn:ICSRr2:EquivalentSubstance.quantity
bridg:ProductRelationship.typeCode
typeCode
bridg:ProductRelationship.typeCode
false
bridg:ProductRelationship.typeCode
A coded value specifying the kind of relationship a product has with another product.
bridg:ProductRelationship.typeCode
lot
bridg:ProductRelationship.typeCode
content
bridg:ProductRelationship.typeCode
kind
bridg:ProductRelationship.typeCode
part
bridg:ProductRelationship.typeCode
ingredient
bridg:ProductRelationship.typeCode
package
bridg:ProductRelationship.typeCode
assembly
bridg:ProductRelationship.typeCode
specialized
bridg:ProductRelationship.typeCode
equivalent
bridg:ProductRelationship.typeCode
urn:CTRv1.0:ProductRelationship.typeCode
in R_Product
bridg:ProductRelationship.typeCode
urn:ICSRr2:SpecializedKind.code
in R_Product
bridg:ProductRelationship.typeCode
urn:ICSRr2:EquivalentEntity.code
bridg:QualifiedPerson.certificateLicenseText
certificateLicenseText
bridg:QualifiedPerson.certificateLicenseText
false
bridg:QualifiedPerson.certificateLicenseText
A character string that describes the specific credentials of the qualified person.
bridg:QualifiedPerson.certificateLicenseText
MD from the John Hopkins University School of Medicine
bridg:QualifiedPerson.certificateLicenseText
Medical license from the state of Maryland
bridg:QualifiedPerson.certificateLicenseText
Certification from the American Board of Pediatrics
bridg:QualifiedPerson.certificateLicenseText
urn:AE:Reporter.qualificationForReporting
bridg:QualifiedPerson.certificateLicenseText
urn:CTGOV:Overall_State_Officials_-_Degree
bridg:QualifiedPerson.certificateLicenseText
urn:CTGOV:Central_Contact_-_Degrees
bridg:QualifiedPerson.certificateLicenseText
urn:CTGOV:Investigators_-_Degrees
bridg:QualifiedPerson.certificateLicenseText
urn:CTGOV:Facility_Contact_-_Degree
bridg:QualifiedPerson.certificateLicenseText
urn:CTR_Rr2:Investigator_qualifications
bridg:QualifiedPerson.certificateLicenseText
urn:CTRPv1.0:HealthCareProvider.certificateLicenseText
bridg:QualifiedPerson.certificateLicenseText
urn:CTRPv3.8:HealthCareProvider.certificateLicenseText
bridg:QualifiedPerson.certificateLicenseText
urn:CTRv1.0:QualifiedPerson.certificateLicenseText
bridg:QualifiedPerson.effectiveDateRange
effectiveDateRange
bridg:QualifiedPerson.effectiveDateRange
false
bridg:QualifiedPerson.effectiveDateRange
The date (and time) span for when the qualification of this person is active.
bridg:QualifiedPerson.effectiveDateRange
urn:CTGOV:Investigators_-_Degrees
bridg:QualifiedPerson.effectiveDateRange
urn:CTGOV:Central_Contact_-_Degrees
bridg:QualifiedPerson.effectiveDateRange
urn:CTGOV:Overall_State_Officials_-_Degree
bridg:QualifiedPerson.effectiveDateRange
urn:CTGOV:Facility_Contact_-_Degree
bridg:QualifiedPerson.effectiveDateRange
urn:CTRv1.0:QualifiedPerson.effectiveDateRange
bridg:QualifiedPerson.identifier
identifier
bridg:QualifiedPerson.identifier
false
bridg:QualifiedPerson.identifier
A unique symbol that establishes identity of the qualified person.
bridg:QualifiedPerson.identifier
The identifier assigned in the NCI investigator registry (National Cancer Institute Principal Investigator Identifier Number) to a physician approved for conducting a clinical study.
bridg:QualifiedPerson.identifier
urn:C3PRv2.9:Investigator.assignedIdentifier
bridg:QualifiedPerson.identifier
urn:C3PRv2.9:RemoteResearchStaff.externalId
bridg:QualifiedPerson.identifier
urn:CTGOV:Overall_State_Officials_-_Degree
bridg:QualifiedPerson.identifier
urn:CTGOV:Facility_Contact_-_Degree
bridg:QualifiedPerson.identifier
urn:CTGOV:Investigators_-_Degrees
bridg:QualifiedPerson.identifier
urn:CTGOV:Central_Contact_-_Degrees
bridg:QualifiedPerson.identifier
urn:CTRv1.0:QualifiedPerson.identifier
bridg:QualifiedPerson.identifier
urn:LabViewer2.2:Investigator.identifier
bridg:QualifiedPerson.typeCode
typeCode
bridg:QualifiedPerson.typeCode
false
bridg:QualifiedPerson.typeCode
A coded value specifying the kind of qualification a person has.
bridg:QualifiedPerson.typeCode
license
bridg:QualifiedPerson.typeCode
academic degree
bridg:QualifiedPerson.typeCode
urn:CTGOV:Overall_State_Officials_-_Degree
bridg:QualifiedPerson.typeCode
urn:CTGOV:Central_Contact_-_Degrees
bridg:QualifiedPerson.typeCode
urn:CTGOV:Facility_Contact_-_Degree
bridg:QualifiedPerson.typeCode
urn:CTGOV:Investigators_-_Degrees
bridg:QualifiedPerson.typeCode
urn:CTRv1.0:QualifiedPerson.typeCode
in IndividualCaseSafetyReport
bridg:QualifiedPerson.typeCode
urn:ICSRr2:QualifiedEntity.code
bridg:RandomizationBookEntry.positionFilledIndicator
positionFilledIndicator
bridg:RandomizationBookEntry.positionFilledIndicator
false
bridg:RandomizationBookEntry.positionFilledIndicator
Specifies whether the position is filled by an experimental unit assignment.
bridg:RandomizationBookEntry.positionFilledIndicator
urn:C3PR:StratumGroup.currentPosition
bridg:RandomizationBookEntry.positionNumber
positionNumber
bridg:RandomizationBookEntry.positionNumber
false
bridg:RandomizationBookEntry.positionNumber
An integer specifying the value of a numerical sequence for a stratum group that should be used to assign an experimental unit to an arm or a portion of an arm.
bridg:RandomizationBookEntry.positionNumber
StratumGroup#: 0; Position: 0; Arm/Portion of Arm: A
bridg:RandomizationBookEntry.positionNumber
StratumGroup#: 0; Position: 1; Arm/Portion of Arm: B
bridg:RandomizationBookEntry.positionNumber
If 2 experimental units fall in the same Stratum Group i.e. say 0 in the above example
bridg:RandomizationBookEntry.positionNumber
the first will be assigned Arm A because the current position would be 0 and the 2nd would be assigned Arm B since the current position would be incremented by 1 each time an assignment happens.
bridg:RandomizationBookEntry.positionNumber
urn:C3PR:BookRandomizationEntry.position
bridg:RandomizationBookEntry.positionNumber
urn:C3PRv2.9:BookRandomizationEntry.position
bridg:ReferenceResult.comment
comment
bridg:ReferenceResult.comment
false
bridg:ReferenceResult.comment
Additional description of the reference result.
bridg:ReferenceResult.comment
urn:CTOM:DiseaseResponse.commentText
bridg:ReferenceResult.comment
urn:CTRv1.0:ReferenceResult.comment
bridg:ReferenceResult.comment
urn:Lab:LabResult.referenceRangeComments
bridg:ReferenceResult.comment
urn:LabViewer2.2:LaboratoryResult.referenceRangeComment
bridg:ReferenceResult.comment
urn:SDTM_IGv3.1.1:CO.COVAL
bridg:ReferenceResult.fastingStatusIndicator
fastingStatusIndicator
bridg:ReferenceResult.fastingStatusIndicator
false
bridg:ReferenceResult.fastingStatusIndicator
Specifies whether the result applies to when the subject had abstained from eating when the specimen is obtained.
bridg:ReferenceResult.fastingStatusIndicator
urn:BRIDGSCC:Model_Integrity
bridg:ReferenceResult.fastingStatusIndicator
urn:CTRv1.0:ReferenceResult.fastingStatusIndicator
bridg:ReferenceResult.populationScopeCode
populationScopeCode
bridg:ReferenceResult.populationScopeCode
false
bridg:ReferenceResult.populationScopeCode
A coded value specifying the type of subjects to which this reference result applies.
bridg:ReferenceResult.populationScopeCode
adult males
bridg:ReferenceResult.populationScopeCode
adult females
bridg:ReferenceResult.populationScopeCode
minor males
bridg:ReferenceResult.populationScopeCode
minor females
bridg:ReferenceResult.populationScopeCode
urn:BRIDGSCC:Model_Integrity
bridg:ReferenceResult.populationScopeCode
urn:CTRv1.0:ReferenceResult.populationScopeCode
bridg:ReferenceResult.referenceTypeCode
referenceTypeCode
bridg:ReferenceResult.referenceTypeCode
false
bridg:ReferenceResult.referenceTypeCode
A coded value specifying the kind of reference, i.e. how it is to be used or what its purpose is.
bridg:ReferenceResult.referenceTypeCode
normal range
bridg:ReferenceResult.referenceTypeCode
limit of quantitation
bridg:ReferenceResult.referenceTypeCode
clinical concern range
bridg:ReferenceResult.referenceTypeCode
data checking range
bridg:ReferenceResult.referenceTypeCode
alert range
bridg:ReferenceResult.referenceTypeCode
urn:CTRv1.0:ReferenceResult.referenceTypeCode
bridg:ReferenceResult.referenceTypeCode
urn:SDTM_IGv3.1.2:LB.LBORNLO
bridg:ReferenceResult.referenceTypeCode
urn:SDTM_IGv3.1.2:LB.LBSTNRHI
bridg:ReferenceResult.referenceTypeCode
urn:SDTM_IGv3.1.2:PC.PCLLOQ
bridg:ReferenceResult.referenceTypeCode
urn:SDTM_IGv3.1.2:LB.LBORNHI
bridg:ReferenceResult.referenceTypeCode
urn:SDTM_IGv3.1.2:LB.LBSTNRC
bridg:ReferenceResult.referenceTypeCode
urn:SDTM_IGv3.1.2:LB.LBSTNRLO
bridg:ReferenceResult.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:ReferenceResult.targetAnatomicSiteCode
false
bridg:ReferenceResult.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of a reference result.
bridg:ReferenceResult.targetAnatomicSiteCode
Arm for skin rash
bridg:ReferenceResult.targetAnatomicSiteCode
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:ReferenceResult.targetAnatomicSiteCode
urn:CTOM:LesionDescription.contactAnatomicSiteCodeSystem
bridg:ReferenceResult.targetAnatomicSiteCode
urn:CTOM:LesionDescription.contactAnatomicSiteCode
bridg:ReferenceResult.targetAnatomicSiteCode
urn:CTRv1.0:ReferenceResult.targetAnatomicSiteCode
bridg:ReferenceResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:ReferenceResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:ReferenceResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:ReferenceResult.targetAnatomicSiteCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
targetAnatomicSiteLateralityCode
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
false
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
A coded value specifying the side of the body (or a paired organ) that is a target site for a result.
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
bilateral
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
left
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
right
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
This attribute is deprecated in BRIDG 3.1 since the only source use case for splitting out laterality from anatomic site comes from CTOM. All other source models had these concepts combined in one attribute. Therefore it was determined to combine these attributes to match the majority of use cases.
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
urn:CTRv1.0:ReferenceResult.targetAnatomicSiteLateralityCode
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:ReferenceResult.targetAnatomicSiteLateralityCode
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:ReferenceResult.value
value
bridg:ReferenceResult.value
false
bridg:ReferenceResult.value
A reference for some measurement that a physician or other health professional can use to interpret a set of results for a particular experimental unit.
bridg:ReferenceResult.value
For systolic blood pressure
bridg:ReferenceResult.value
ReferenceResult.value(ANY) would be constrained to IVL<PQ> and would = 110-130 mm[Hg]
bridg:ReferenceResult.value
urn:CDASHv1.1:LB.LBORNRHI
bridg:ReferenceResult.value
urn:CDASHv1.1:LB.LBORNRLO
bridg:ReferenceResult.value
urn:CTOM:ClinicalResult.labReferenceRangeCode
bridg:ReferenceResult.value
urn:CTRv1.0:ReferenceResult.value
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953862:Lab_Results.Serum_Creatinine_Upper_Limit_of_Normal
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953117:Lab_Results.What_is_the_upper_limit_of_normal_value_of_serum_creatinine?
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2954133:Lab_Results.Serum_Immunoglobin_Upper_Limit_of_Normal
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2597015:Lab_Results.Lactate_Dehydrogenase_ULN
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953277:Lab_Results.Unit_of_measure:_lambda
SGOT?
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953111:Lab_Results.What_is_the_upper_limit_of_normal_value_of_AST
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2963544:Lab_Results.What_is_the_upper_limit_of_normal_value_of_beta-2-microglobulin_protein?
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953866:Lab_Results.LDH_Upper_Limit_of_Normal_Unit_of_Measure
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953113:Lab_Results.What_is_the_upper_limit_of_normal_value_of_total_serum_bilirubin?
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953268:Lab_Results.Upper_limit_of_normal_for_lambda_free_light_chain:
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953266:Lab_Results.upper_limit_of_normal_for_kappa_free_light_chain:
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2953270:Lab_Results.Unit_of_measure:_kappa
bridg:ReferenceResult.value
urn:HCTv1.0:CDE_2954096:Lab_Results.Specify_the_serum_immunoglobin_lower_limit_of_normal_value:
bridg:ReferenceResult.value
urn:Lab:LabResult.referenceRangeHigh
bridg:ReferenceResult.value
urn:Lab:LaboratoryResult.referenceTextList
bridg:ReferenceResult.value
urn:Lab:LabResult.referenceRangeLow
bridg:ReferenceResult.value
urn:Lab:LabResult.referenceTextList
bridg:ReferenceResult.value
urn:LabViewer2.2:LaboratoryResult.referenceRangeHigh
bridg:ReferenceResult.value
urn:LabViewer2.2:LaboratoryResult.referenceRangeLow
bridg:ReferenceResult.value
urn:NCI_CRF_Standard:CDE_2841221v1.0:_Test_Result_Low_Test_Reference_Range_Number
bridg:ReferenceResult.value
urn:NCI_CRF_Standard:CDE_2841212v1.0:_Test_Result_High_Test_Reference_Range_Number
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.1:LB.LBORNRHI
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.1:LB.LBORNRLO
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.1:LB.LBSTNRC
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.1:LB.LBSTNRLO
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.1:LB.LBSTNRHI
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.2:LB.LBORNRHI
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.2:LB.LBSTNRHI
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.2:PC.PCLLOQ
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.2:LB.LBSTNRC
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.2:LB.LBSTNRLO
bridg:ReferenceResult.value
urn:SDTM_IGv3.1.2:LB.LBORNRLO
bridg:ReferenceResult.valueTypeCode
valueTypeCode
bridg:ReferenceResult.valueTypeCode
false
bridg:ReferenceResult.valueTypeCode
A coded value specifying the kind of clinical result to which this reference result must be associated.
bridg:ReferenceResult.valueTypeCode
For a blood pressure measurement
bridg:ReferenceResult.valueTypeCode
the valueTypeCode may be systolic or diastolic.
bridg:ReferenceResult.valueTypeCode
urn:CTOM:ClinicalResult.value
bridg:ReferenceResult.valueTypeCode
urn:CTRv1.0:ReferenceResult.valueTypeCode
bridg:ReferenceToStudyResults.citationDescription
citationDescription
bridg:ReferenceToStudyResults.citationDescription
false
bridg:ReferenceToStudyResults.citationDescription
A biblographical reference in a format acceptable to the registration authority.
bridg:ReferenceToStudyResults.citationDescription
Studies performed in the United States may be required to conform to the National Library of Medicine's MEDLINE format.
bridg:ReferenceToStudyResults.citationDescription
urn:CTGOV:Citation
bridg:ReferenceToStudyResults.citationDescription
urn:CTRv1.0:ReferenceToStudyResults.citationDescription
bridg:ReferenceToStudyResults.linkPageDescription
linkPageDescription
bridg:ReferenceToStudyResults.linkPageDescription
false
bridg:ReferenceToStudyResults.linkPageDescription
The textual representation of the linked page.
bridg:ReferenceToStudyResults.linkPageDescription
If the page being linked is the protocol's home page on the sponsor's Web site
bridg:ReferenceToStudyResults.linkPageDescription
include the words "Click here for more information about this study:" and provide the name of the protocol.
bridg:ReferenceToStudyResults.linkPageDescription
urn:CTGOV:Links_Description
bridg:ReferenceToStudyResults.linkPageDescription
urn:CTRv1.0:ReferenceToStudyResults.linkPageDescription
bridg:ReferenceToStudyResults.publicationIdentifier
publicationIdentifier
bridg:ReferenceToStudyResults.publicationIdentifier
false
bridg:ReferenceToStudyResults.publicationIdentifier
A unique symbol that establishes identity to a publication that cites this study's results.
bridg:ReferenceToStudyResults.publicationIdentifier
10987815 is the unique PubMed Identifier (PMID) for the citation in MEDLINE.
bridg:ReferenceToStudyResults.publicationIdentifier
urn:CTGOV:MEDLINE_Identifier
bridg:ReferenceToStudyResults.publicationIdentifier
urn:CTRv1.0:ReferenceToStudyResults.publicationIdentifier
bridg:ReferenceToStudyResults.publicationName
publicationName
bridg:ReferenceToStudyResults.publicationName
false
bridg:ReferenceToStudyResults.publicationName
A non-unique textual identifier specifying the source of the publication identifier.
bridg:ReferenceToStudyResults.publicationName
MEDLINE is the source for PMID 10987815
bridg:ReferenceToStudyResults.publicationName
urn:CTRv1.0:ReferenceToStudyResults.publicationName
bridg:ReferenceToStudyResults.publicationName
urn:PRM:PublishedResults.title
bridg:ReferenceToStudyResults.uniformResourceLocator
uniformResourceLocator
bridg:ReferenceToStudyResults.uniformResourceLocator
false
bridg:ReferenceToStudyResults.uniformResourceLocator
A complete reference to a website (including http://) that is directly relevant to the study.
bridg:ReferenceToStudyResults.uniformResourceLocator
http://www.alzheimers.org/
bridg:ReferenceToStudyResults.uniformResourceLocator
urn:CTGOV:Links_URL
bridg:ReferenceToStudyResults.uniformResourceLocator
urn:CTRv1.0:ReferenceToStudyResults.uniformResourceLocator
bridg:RegistrationCenter.telecomAddress
telecomAddress
bridg:RegistrationCenter.telecomAddress
false
bridg:RegistrationCenter.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of a registration center.
bridg:RegistrationCenter.telecomAddress
The phone number to call to request that a subject be registered and randomized on a study.
bridg:RegistrationCenter.telecomAddress
urn:C3PR:PhoneCallRandomization.phoneNumber
bridg:RegistrationCenter.telecomAddress
urn:C3PRv2.9:PhoneCallRandomization.phoneNumber
bridg:RegistrationCenter.telecomAddress
urn:CTRv1.0:RegistrationCenter.telecomAddress
bridg:RegulatoryApplication.identifier
identifier
bridg:RegulatoryApplication.identifier
false
bridg:RegulatoryApplication.identifier
A unique symbol that establishes identity of the regulatory application.
bridg:RegulatoryApplication.identifier
urn:CTGOV:IND/IDE_Protocol?
bridg:RegulatoryApplication.identifier
urn:CTGOV:IND/IDE_Number
bridg:RegulatoryApplication.identifier
urn:CTOM:StudyAgent.investigationalNewDrugIdentifier
bridg:RegulatoryApplication.identifier
urn:CTR_Rr2:PIP_Decision_number
bridg:RegulatoryApplication.identifier
urn:CTRPv1.0:StudyProtocol.indIdeIndicator
bridg:RegulatoryApplication.identifier
urn:CTRPv1.0:ObservationalStudyProtocol.indIdeIndicator
bridg:RegulatoryApplication.identifier
urn:CTRPv3.8:StudyIndIde.indIdeNumber
IND/IDE number suffix
bridg:RegulatoryApplication.identifier
urn:CTRR:IND/IDE_Protocol
bridg:RegulatoryApplication.identifier
urn:CTRR:Regulatory_Investigational_Product_Application_Identifier
bridg:RegulatoryApplication.identifier
urn:CTRRr3:RegulatoryApplication.identifier
bridg:RegulatoryApplication.identifier
urn:CTRv1.0:RegulatoryApplication.identifier
bridg:RegulatoryApplication.identifier
urn:HCTv1.0:MD_Anderson_Specific_Content:_Protocol_.IND_number
bridg:RegulatoryApplication.identifier
urn:HSDBv1.0:[IND/IDE]_.Number
bridg:RegulatoryApplication.identifier
urn:caAERSv2.2:InvestigationalNewDrug.indNumber
bridg:RegulatoryApplication.typeCode
typeCode
bridg:RegulatoryApplication.typeCode
false
bridg:RegulatoryApplication.typeCode
A coded value specifying the kind of regulatory application.
bridg:RegulatoryApplication.typeCode
New Drug Application
bridg:RegulatoryApplication.typeCode
510k
bridg:RegulatoryApplication.typeCode
Veterinary New Drug Submission
bridg:RegulatoryApplication.typeCode
Each product type will be supported by a different application type.
bridg:RegulatoryApplication.typeCode
urn:CTRPv3.8:StudyIndIde.indIdeTypeCode
bridg:RegulatoryApplication.typeCode
urn:CTRR:IND/IDE_Indicator
bridg:RegulatoryApplication.typeCode
urn:CTRRr3:RegulatoryApplication.typeCode
bridg:RegulatoryApplication.typeCode
urn:CTRv1.0:RegulatoryApplication.typeCode
bridg:RegulatoryApplication.typeCode
urn:HSDBv1.0:[IND/IDE].Type
bridg:RegulatoryApplication.typeCode
urn:RPS1:Application.code
bridg:RegulatoryApplicationSponsor.effectiveDateRange
effectiveDateRange
bridg:RegulatoryApplicationSponsor.effectiveDateRange
false
bridg:RegulatoryApplicationSponsor.effectiveDateRange
The date and time span for when the regulatory application sponsor is active.
bridg:RegulatoryApplicationSponsor.effectiveDateRange
urn:CTRv1.0:RegulatoryApplicationSponsor.effectiveDateRange
New content
bridg:RegulatoryApplicationSponsor.effectiveDateRange
urn:RPS2:
bridg:RegulatoryAssessment.completionDate
completionDate
bridg:RegulatoryAssessment.completionDate
false
bridg:RegulatoryAssessment.completionDate
The date (and time) on which this particular assessment is completed.
bridg:RegulatoryAssessment.completionDate
urn:CTGOV:Expanded_Access_Status
bridg:RegulatoryAssessment.completionDate
urn:CTR_Rr2:IEC_Opinion_date
bridg:RegulatoryAssessment.completionDate
urn:CTRR:Expanded_access_indicator
bridg:RegulatoryAssessment.completionDate
urn:CTRRr3:RegulatoryAssessment.assessmentDate
bridg:RegulatoryAssessment.completionDate
urn:CTRv1.0:RegulatoryAssessment.completionDate
in R_Product
bridg:RegulatoryAssessment.completionDate
urn:ICSRr2:Author2.time
in R_Product
bridg:RegulatoryAssessment.completionDate
urn:ICSRr2:Approval.effectiveTime
bridg:RegulatoryAssessment.expectedResubmissionDate
expectedResubmissionDate
bridg:RegulatoryAssessment.expectedResubmissionDate
false
bridg:RegulatoryAssessment.expectedResubmissionDate
The date on which the resubmission of the regulatory application is expected.
bridg:RegulatoryAssessment.expectedResubmissionDate
Used only when RegulatoryAssessment.statusCode is not complete.
Regulatory authorities typically assign a resubmission deadline such as 30 days.
bridg:RegulatoryAssessment.expectedResubmissionDate
urn:CTRRr3:RegulatoryAssessment.expectedResubmissionDate
bridg:RegulatoryAssessment.identifier
identifier
bridg:RegulatoryAssessment.identifier
false
bridg:RegulatoryAssessment.identifier
A unique symbol that establishes identity of the regulatory assessment.
bridg:RegulatoryAssessment.identifier
New Drug Application (NDA) number
bridg:RegulatoryAssessment.identifier
Investigational New Drug (IND) number
bridg:RegulatoryAssessment.identifier
Biologic License Application (BLA)
bridg:RegulatoryAssessment.identifier
Premarket Approval (PMA)
bridg:RegulatoryAssessment.identifier
510K
bridg:RegulatoryAssessment.identifier
urn:AE:Authorization.approvalId
bridg:RegulatoryAssessment.identifier
urn:CTR_Rr2:MA_number
bridg:RegulatoryAssessment.identifier
urn:CTR_Rr2:Orphan_drug_number
bridg:RegulatoryAssessment.identifier
urn:CTR_Rr2:Manufacturer_authorisation_number
bridg:RegulatoryAssessment.identifier
urn:CTRPv1.0:TherapeuticProduct.identifier
bridg:RegulatoryAssessment.identifier
urn:CTRRr3:RegulatoryAssessment.identifier
bridg:RegulatoryAssessment.identifier
urn:CTRv1.0:RegulatoryAssessment.identifier
in R_Product
bridg:RegulatoryAssessment.identifier
urn:ICSRr2:Approval.id
bridg:RegulatoryAssessment.reasonCode
reasonCode
bridg:RegulatoryAssessment.reasonCode
false
bridg:RegulatoryAssessment.reasonCode
A coded value specifying the rationale for a regulatory designation.
bridg:RegulatoryAssessment.reasonCode
urn:CTR_Rr2:Reason_for_no_authorisation
bridg:RegulatoryAssessment.reasonCode
urn:CTR_Rr2:IEC_Opinion_not_favourable_reasons
bridg:RegulatoryAssessment.reasonCode
urn:CTRRr3:RegulatoryAssessment.assessmentReasonCode
bridg:RegulatoryAssessment.reasonCode
urn:CTRv1.0:RegulatoryAssessment.reasonCode
bridg:RegulatoryAssessment.resultCode
resultCode
bridg:RegulatoryAssessment.resultCode
false
bridg:RegulatoryAssessment.resultCode
A coded value specifying the regulatory designation made by the regulatory authority.
bridg:RegulatoryAssessment.resultCode
For regular submissions the code can be: approved
bridg:RegulatoryAssessment.resultCode
not approvable
bridg:RegulatoryAssessment.resultCode
approvable
bridg:RegulatoryAssessment.resultCode
complete response or cleared.
bridg:RegulatoryAssessment.resultCode
For expanded access submissions the code can be: Available
bridg:RegulatoryAssessment.resultCode
No longer available
bridg:RegulatoryAssessment.resultCode
Temporarily not available
bridg:RegulatoryAssessment.resultCode
or Approved for marketing.
bridg:RegulatoryAssessment.resultCode
For some submissions, there are business processes that will make "default" action based on timelines --i.e., if no action is taken, then the submission is "approved".
For a submission, there may be multiple regulatory assessments that correspond to the state transitions for a submission, but only one regulatory assessment is true at a given time. A submission can first be "approvable" and then when the data is complete, a new regulatory assessment can be made that is "approved".
bridg:RegulatoryAssessment.resultCode
urn:CTGOV:Expanded_Access_Status
bridg:RegulatoryAssessment.resultCode
urn:CTR_Rr2:GMP_MP_Auth_granted
bridg:RegulatoryAssessment.resultCode
urn:CTR_Rr2:IEC_Opinion_Given
bridg:RegulatoryAssessment.resultCode
urn:CTRPv3.8:StudyIndIde.expandedAccessStatusCode
bridg:RegulatoryAssessment.resultCode
urn:CTRR:Expanded_access_indicator
bridg:RegulatoryAssessment.resultCode
urn:CTRRr3:RegulatoryAssessment.assessmentCode
bridg:RegulatoryAssessment.resultCode
urn:CTRRr3:StudyAgent.expandedAccessStatusCode
bridg:RegulatoryAssessment.resultCode
urn:CTRv1.0:RegulatoryAssessment.resultCode
bridg:RegulatoryAssessment.statusCode
statusCode
bridg:RegulatoryAssessment.statusCode
false
bridg:RegulatoryAssessment.statusCode
A coded value specifying the phase in the lifecycle of the assessment.
bridg:RegulatoryAssessment.statusCode
pending
bridg:RegulatoryAssessment.statusCode
complete
bridg:RegulatoryAssessment.statusCode
urn:CTRRr3:RegulatoryAssessment.statusCode
bridg:RegulatoryAssessment.typeCode
typeCode
bridg:RegulatoryAssessment.typeCode
false
bridg:RegulatoryAssessment.typeCode
A coded value specifying the approval process used by the regulatory authority.
bridg:RegulatoryAssessment.typeCode
FDA's Center for Devices and Radiological Health (CDRH) Process
bridg:RegulatoryAssessment.typeCode
FDA's Center for Drug Evaluation and Research (CDER) Process
bridg:RegulatoryAssessment.typeCode
urn:CTRv1.0:RegulatoryAssessment.typeCode
bridg:RegulatoryAssessment.typeCode
urn:HSDBv1.0:[IND/IDE]_.Grantor
in R_Product
bridg:RegulatoryAssessment.typeCode
urn:ICSRr2:Approval.code
bridg:RegulatoryAuthority.effectiveDateRange
effectiveDateRange
bridg:RegulatoryAuthority.effectiveDateRange
false
bridg:RegulatoryAuthority.effectiveDateRange
The date and time span for when the regulatory authority is active.
bridg:RegulatoryAuthority.effectiveDateRange
urn:CTRPv1.0:RegulatoryAuthority.statusDateRange
bridg:RegulatoryAuthority.effectiveDateRange
urn:CTRPv1.0:RegulatoryAuthority.statusCode
bridg:RegulatoryAuthority.effectiveDateRange
urn:CTRv1.0:RegulatoryAuthority.effectiveDateRange
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
jurisdictionAuthorityCode
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
false
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
A coded value specifying the type of governance over which an authority has to make laws and enforce them.
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
The Food and Drug Administration (FDA) exercises responsibility for pharmacovigilance (jurisdictionAuthorityCode) in the United States (Place.identifierCode).
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTR_Rr2:SUSAR_Reporting_to_EVCTM
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTR_Rr2:SUSAR_Reporting_to_NCAs
Scientific Advice from CHMP
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTR_Rr2:SA
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTR_Rr2:SA_from_NCA
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTRPv3.8:RegulatoryAuthority.jurisdictionCode
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTRRr3:RegulatoryAuthority.jurisdictionCode
bridg:RegulatoryAuthority.jurisdictionAuthorityCode
urn:CTRv1.0:RegulatoryAuthority.jurisdictionAuthorityCode
bridg:RelevantRegulation.applicableIndicator
applicableIndicator
bridg:RelevantRegulation.applicableIndicator
false
bridg:RelevantRegulation.applicableIndicator
Specifies whether this study must be registered as required by applicable laws.
bridg:RelevantRegulation.applicableIndicator
Section 801 Clinical Trial
bridg:RelevantRegulation.applicableIndicator
Under US Public Law 110-85, Title VIII, Section 801, applicable drug trials include controlled clinical investigations, other than Phase I investigations, of a drug or biologic subject to US FDA regulation. Applicable device clinical trials are controlled trials with health outcomes of devices subject to FDA regulation, other than small feasibility studies, and pediatric postmarket surveillance.
bridg:RelevantRegulation.applicableIndicator
urn:CTRPv3.8:StudyProtocol.FDAregulatedIndicator
bridg:RelevantRegulation.applicableIndicator
urn:CTRPv3.8:StudyProtocol.section801Indicator
bridg:RelevantRegulation.applicableIndicator
urn:CTRRr3:Study.applicableClinicalTrialIndicator
bridg:RelevantRegulation.code
code
bridg:RelevantRegulation.code
false
bridg:RelevantRegulation.code
A coded value specifying a regulation that requires the study to be registered.
bridg:RelevantRegulation.code
US Food and Drug Administration regulation under section 351 of the Public Health Service Act or any of the following sections of the Federal Food
bridg:RelevantRegulation.code
Drug and Cosmetic Act: 505
bridg:RelevantRegulation.code
510(k)
bridg:RelevantRegulation.code
515
bridg:RelevantRegulation.code
520(m)
bridg:RelevantRegulation.code
and 522.
bridg:RelevantRegulation.code
urn:CTRRr3:Study.applicableRegulationCode
bridg:ReportReceiver.receivedDate
receivedDate
bridg:ReportReceiver.receivedDate
false
bridg:ReportReceiver.receivedDate
The date (and time) on which the report was received.
bridg:ReportReceiver.receivedDate
urn:CTRv1.0:ReportReceiver.receivedDate
in IndividualCaseSafetyReport
bridg:ReportReceiver.receivedDate
urn:ICSRr2:PrimaryInformationRecipient.time
bridg:ReportReceiver.receivedIndicator
receivedIndicator
bridg:ReportReceiver.receivedIndicator
false
bridg:ReportReceiver.receivedIndicator
Specifies whether the receiver received the report.
bridg:ReportReceiver.receivedIndicator
urn:CTRv1.0:ReportReceiver.receivedIndicator
in IndividualCaseSafetyReport
bridg:ReportReceiver.receivedIndicator
urn:ICSRr2:PrimaryInformationRecipient.negationInd
bridg:ReportVersion.communicationModeCode
communicationModeCode
bridg:ReportVersion.communicationModeCode
false
bridg:ReportVersion.communicationModeCode
A coded value specifying the form in which the report is transmitted.
bridg:ReportVersion.communicationModeCode
physically present
bridg:ReportVersion.communicationModeCode
over the telephone
bridg:ReportVersion.communicationModeCode
written communication
bridg:ReportVersion.communicationModeCode
electronic
bridg:ReportVersion.communicationModeCode
urn:AE:ReportReceipt.modeCode
bridg:ReportVersion.communicationModeCode
urn:CTRv1.0:ReportVersion.communicationModeCode
in IndividualCaseSafetyReport
bridg:ReportVersion.communicationModeCode
urn:ICSRr2:PrimaryInformationRecipient.modeCode
bridg:ReportVersion.dueDate
dueDate
bridg:ReportVersion.dueDate
false
bridg:ReportVersion.dueDate
The date (and time) on which the report is expected or scheduled to be submitted.
bridg:ReportVersion.dueDate
urn:CTRv1.0:ReportVersion.dueDate
bridg:ReportVersion.dueDate
urn:caAERSv2.2:ReportVersion.dueOn
bridg:ReportVersion.dueDate
urn:caAERSv2.2:Report.dueDate
bridg:ReportVersion.physicianSignOffIndicator
physicianSignOffIndicator
bridg:ReportVersion.physicianSignOffIndicator
false
bridg:ReportVersion.physicianSignOffIndicator
Specifies whether the physician has reviewed and signed off on a version of a report.
bridg:ReportVersion.physicianSignOffIndicator
Theoretically speaking, the physicianSignoffIndicator could be derived from the existence of an authenticating person for the report. However, authenticating person is not represented in the BRIDG model because this use case has not yet been formally presented to BRIDG. If and when this use case is presented to BRIDG the physicianSignoffIndicator will be marked as derived, but for now this attribute will remain as not derivable.
bridg:ReportVersion.physicianSignOffIndicator
urn:CTRv1.0:ReportVersion.physicianSignOffIndicator
bridg:ReportVersion.physicianSignOffIndicator
urn:caAERSv2.2:ReportVersion.physicianSignOff
bridg:ResearchOrganization.effectiveDateRange
effectiveDateRange
bridg:ResearchOrganization.effectiveDateRange
false
bridg:ResearchOrganization.effectiveDateRange
The date (and time) span for when the research organization is active.
bridg:ResearchOrganization.effectiveDateRange
urn:CTRPv1.0:ResearchOrganization.statusCode
bridg:ResearchOrganization.effectiveDateRange
urn:CTRPv1.0:ResearchOrganization.statusDateRange
bridg:ResearchOrganization.effectiveDateRange
urn:CTRv1.0:ResearchOrganization.effectiveDateRange
bridg:ResearchOrganization.effectiveDateRange
urn:HL7SP:Service_Provider.statusCode
bridg:ResearchOrganization.effectiveDateRange
urn:HL7SP:Service_Provider.effectiveTime
bridg:ResearchOrganization.typeCode
typeCode
bridg:ResearchOrganization.typeCode
false
bridg:ResearchOrganization.typeCode
A coded value specifying the kind of research organization.
bridg:ResearchOrganization.typeCode
cancer center
bridg:ResearchOrganization.typeCode
institute
bridg:ResearchOrganization.typeCode
drug company
bridg:ResearchOrganization.typeCode
clinical center
bridg:ResearchOrganization.typeCode
urn:CTRPv1.0:ResearchOrganization.typeCode
bridg:ResearchOrganization.typeCode
urn:CTRPv3.8:ResearchOrganization.typeCode
bridg:ResearchOrganization.typeCode
urn:CTRv1.0:ResearchOrganization.typeCode
bridg:ResearchOrganization.typeCode
urn:HL7SP:Service_Provider.code
bridg:ResearchStaff.effectiveDateRange
effectiveDateRange
bridg:ResearchStaff.effectiveDateRange
false
bridg:ResearchStaff.effectiveDateRange
The date (and time) span for when the research staff is active.
bridg:ResearchStaff.effectiveDateRange
urn:CTRPv1.0:ClinicalResearchStaff.statusCode
bridg:ResearchStaff.effectiveDateRange
urn:CTRPv1.0:ClinicalResearchStaff.statusDateRange
bridg:ResearchStaff.effectiveDateRange
urn:CTRv1.0:ResearchStaff.effectiveDateRange
bridg:ResearchStaff.identifier
identifier
bridg:ResearchStaff.identifier
false
bridg:ResearchStaff.identifier
A unique symbol that establishes identity of the research staff.
bridg:ResearchStaff.identifier
urn:C3PRv2.9:ResearchStaff.assignedIdentifier
bridg:ResearchStaff.identifier
urn:CTRv1.0:ResearchStaff.identifier
bridg:ResearchStaff.identifier
urn:caAERSv2.2:ResearchStaff.nciIdentifier
bridg:ResearchStaff.jobTitle
jobTitle
bridg:ResearchStaff.jobTitle
false
bridg:ResearchStaff.jobTitle
A local name for the research staff's occupation.
bridg:ResearchStaff.jobTitle
urn:CTRRr3:StudyColleague.officialTitle
bridg:ResearchStaff.jobTitle
urn:CTRv1.0:ResearchStaff.jobTitle
bridg:ResearchStaff.jobTitle
urn:caAERSv2.2:Person.title
bridg:ResearchStaff.postalAddress
postalAddress
bridg:ResearchStaff.postalAddress
false
bridg:ResearchStaff.postalAddress
A contact point used to send physical forms of communication to the research staff.
bridg:ResearchStaff.postalAddress
urn:CTRPv1.0:ClinicalResearchStaff.postalAddress
bridg:ResearchStaff.postalAddress
urn:CTRv1.0:ResearchStaff.postalAddress
in IndividualCaseSafetyReport
bridg:ResearchStaff.postalAddress
urn:ICSRr2:AssignedEntity.addr
bridg:ResearchStaff.postalAddress
urn:caAERSv2.2:Address.city___ResearchStaff
bridg:ResearchStaff.postalAddress
urn:caAERSv2.2:Address.zip___ResearchStaff
bridg:ResearchStaff.postalAddress
urn:caAERSv2.2:Address.street___ResearchStaff
bridg:ResearchStaff.postalAddress
urn:caAERSv2.2:Address.state___ResearchStaff
bridg:ResearchStaff.postalAddress
urn:caAERSv2.2:Address.country__ResearchStaff
bridg:ResearchStaff.telecomAddress
telecomAddress
bridg:ResearchStaff.telecomAddress
false
bridg:ResearchStaff.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the research staff.
bridg:ResearchStaff.telecomAddress
NOTE(S):
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:ResearchStaff.telecomAddress
urn:C3PRv2.9:SiteResearchStaff.phoneNumber
bridg:ResearchStaff.telecomAddress
urn:CTRPv1.0:ClinicalResearchStaff.telecomAddress
bridg:ResearchStaff.telecomAddress
urn:CTRv1.0:ResearchStaff.telecomAddress
in IndividualCaseSafetyReport
bridg:ResearchStaff.telecomAddress
urn:ICSRr2:AssignedEntity.telecom
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:SiteResearchStaff.emailAddress
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:SiteResearchStaff.faxNumber
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:PersonContact.ReportPerson.Submitter.contactMechanisms
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:PersonContact.ReportPerson.Reporter.contactMechanisms
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:ResearchStaff.phoneNumber
bridg:ResearchStaff.telecomAddress
urn:caAERSv2.2:ResearchStaff.faxNumber
bridg:Resource.activeIndicator
activeIndicator
bridg:Resource.activeIndicator
false
bridg:Resource.activeIndicator
Specifies whether the resource is active.
bridg:Resource.activeIndicator
urn:CTRPv1.0:StudyResourcing.activeIndicator
bridg:Resource.activeIndicator
urn:CTRv1.0:Resource.activeIndicator
bridg:ResourceProvider.effectiveDateRange
effectiveDateRange
bridg:ResourceProvider.effectiveDateRange
false
bridg:ResourceProvider.effectiveDateRange
The date (and time) span for when the resource provider is active.
bridg:ResourceProvider.effectiveDateRange
urn:CTRPv1.0:ResourceProvider.statusDateRange
bridg:ResourceProvider.effectiveDateRange
urn:CTRPv1.0:ResourceProvider.statusCode
bridg:ResourceProvider.effectiveDateRange
urn:CTRv1.0:ResourceProvider.effectiveDateRange
bridg:ResourceProvider.effectiveDateRange
urn:HL7SP:StudyParticipation_RMIM
bridg:ResourceProvider.identifier
identifier
bridg:ResourceProvider.identifier
false
bridg:ResourceProvider.identifier
A unique symbol that establishes identity of the resource provider.
bridg:ResourceProvider.identifier
urn:C3PR:Study.sponsorCode
bridg:ResourceProvider.identifier
urn:CTOM:Protocol.sponsorCode
bridg:ResourceProvider.identifier
urn:CTRPv1.0:ResourceProvider.identifier
bridg:ResourceProvider.identifier
urn:CTRv1.0:ResourceProvider.identifier
bridg:ResourceProvider.identifier
urn:HL7SP:StudyParticipation_RMIM
bridg:ReviewableUnit.typeCode
typeCode
bridg:ReviewableUnit.typeCode
false
bridg:ReviewableUnit.typeCode
A coded value specifying the kind of reviewable unit.
bridg:ReviewableUnit.typeCode
toxicology
bridg:ReviewableUnit.typeCode
safety
bridg:ReviewableUnit.typeCode
manufacturing
bridg:ReviewableUnit.typeCode
administrative
bridg:ReviewableUnit.typeCode
urn:CTRv1.0:ReviewableUnit.typeCode
bridg:ReviewableUnit.typeCode
urn:RPS1:ReviewableUnit.contents
bridg:SafetyReportVersion.nullificationIndicator
nullificationIndicator
bridg:SafetyReportVersion.nullificationIndicator
false
bridg:SafetyReportVersion.nullificationIndicator
Specifies whether the report cancels a previously sent adverse event.
bridg:SafetyReportVersion.nullificationIndicator
urn:AE:SafetyReport.nullificationReportInd
bridg:SafetyReportVersion.nullificationIndicator
urn:CTRv1.0:SafetyReportVersion.nullificationIndicator
bridg:SafetyReportVersion.nullificationReasonCode
nullificationReasonCode
bridg:SafetyReportVersion.nullificationReasonCode
false
bridg:SafetyReportVersion.nullificationReasonCode
A coded value specifying why the adverse event report is nullified.
bridg:SafetyReportVersion.nullificationReasonCode
urn:AE:NullificationReport.nullificationReasonCode
bridg:SafetyReportVersion.nullificationReasonCode
urn:AE:SafetyReport.reasonCode
bridg:SafetyReportVersion.nullificationReasonCode
urn:CTRv1.0:SafetyReportVersion.nullificationReasonCode
bridg:SafetyReportVersion.subtypeCode
subtypeCode
bridg:SafetyReportVersion.subtypeCode
false
bridg:SafetyReportVersion.subtypeCode
A coded value specifying a further classification of type.
bridg:SafetyReportVersion.subtypeCode
An Adverse Event Report would map to Document.typeCode and the SafetyReportVersion.subtypeCode would map to a 7-day AE Report.
bridg:SafetyReportVersion.subtypeCode
urn:AE:SafetyReport.expeditedReportCriteriaInd
bridg:SafetyReportVersion.subtypeCode
urn:AE:SafetyReport.spontaneousReportInd
bridg:SafetyReportVersion.subtypeCode
urn:AE:SafetyReport.problemType
bridg:SafetyReportVersion.subtypeCode
urn:AE:SafetyReport.reportingCriteriaCode
bridg:SafetyReportVersion.subtypeCode
urn:CTRv1.0:SafetyReportVersion.subtypeCode
in IndividualCaseSafetyReport
bridg:SafetyReportVersion.subtypeCode
urn:ICSRr2:RelatedInvestigation.code
in IndividualCaseSafetyReport
bridg:SafetyReportVersion.subtypeCode
urn:ICSRr2:InvestigativeEvent.code
bridg:SampleSizeConsideration.text
text
bridg:SampleSizeConsideration.text
false
bridg:SampleSizeConsideration.text
A textual or media-based representation of the sample size consideration, including details needed to replicate sample size calculations.
bridg:SampleSizeConsideration.text
"Approximately 100 patients will be randomized to each of the 3 treatment groups. Previous experience with the oral formulation of xanomeline suggests that this sample size has 90% power to detect a 3.0 mean treatment difference in ADAS-Cog (p<.05
bridg:SampleSizeConsideration.text
two-sided)
bridg:SampleSizeConsideration.text
based on a standard deviation of 6.5. Furthermore
bridg:SampleSizeConsideration.text
this sample size has 80% power to detect a 0.36 mean treatment difference in CIBIC+ (p<.05
bridg:SampleSizeConsideration.text
two-sided)
bridg:SampleSizeConsideration.text
based on a standard deviation of 0.9."
bridg:SampleSizeConsideration.text
Details included could be: difference to be detected, variability, assumptions.
bridg:SampleSizeConsideration.text
urn:Statistics_v1.0:SampleSizeConsideration.text
bridg:ScheduledActivity.dateRange
dateRange
bridg:ScheduledActivity.dateRange
false
bridg:ScheduledActivity.dateRange
The date and time span specifying when the activity is scheduled to begin and end.
bridg:ScheduledActivity.dateRange
urn:CTGOV:Anticipated_Study_Completion_Date
bridg:ScheduledActivity.dateRange
urn:HCTv1.0:CDE_3158501:Therapies.Scheduled_infusion_date:
bridg:ScheduledActivity.dateRange
urn:HCTv1.0:CDE_2866945:Therapies.If_this_HSCT_was_postponed__what_is_the_new_estimated_date?
bridg:ScheduledActivity.dateRange
urn:NCI_CRF_Standard:CDE_657v3.0:_Treatment_Projected_Begin_Date
bridg:ScheduledActivity.dateRange
urn:PRM:Period.startDay
bridg:ScheduledActivity.dateRange
urn:PSC:ScheduledEvent.date/idealDate
bridg:ScheduledActivity.dateRange
urn:PSC:Scheduled.date
bridg:ScheduledActivity.dateRange
urn:PSC:ScheduledEventState.scheduled
bridg:ScheduledActivity.dateRange
urn:PSCv2.6:ScheduledStudySegment.startDate
bridg:ScheduledActivity.dateRange
urn:caAERSv2.2:ScheduledNotification.scheduledOn
bridg:ScheduledActivity.idealDateRange
idealDateRange
bridg:ScheduledActivity.idealDateRange
false
bridg:ScheduledActivity.idealDateRange
The date and time span specifying when the activity was originally scheduled to begin and end.
bridg:ScheduledActivity.idealDateRange
This would be the date and time span based on applying the study calendar to a specific subject.
bridg:ScheduledActivity.idealDateRange
urn:PSCv2.6:ScheduledActivity.idealDate
bridg:ScheduledActivity.repetitionNumber
repetitionNumber
bridg:ScheduledActivity.repetitionNumber
false
bridg:ScheduledActivity.repetitionNumber
An integer that identifies the particular occurrence of a repeating activity. The first repetition is defined as '1'.
bridg:ScheduledActivity.repetitionNumber
A PlannedActivity might have a repeatQuantity of 4 which would result in 4 ScheduledActivity with repetitionNumbers of 1
bridg:ScheduledActivity.repetitionNumber
2
bridg:ScheduledActivity.repetitionNumber
3
bridg:ScheduledActivity.repetitionNumber
and 4 respectively.
bridg:ScheduledActivity.repetitionNumber
The ScheduledActivity will repeat at least the minimum number of times and at most, the maximum number of times as defined in PlannedActivity.repeatQuantity.
bridg:ScheduledActivity.repetitionNumber
urn:PSC:Period.repetitions
bridg:ScheduledActivity.repetitionNumber
urn:PSCv2.6:ScheduledActivity.repetitionNumber
bridg:ScheduledActivity.statusChangeReasonCode
statusChangeReasonCode
bridg:ScheduledActivity.statusChangeReasonCode
false
bridg:ScheduledActivity.statusChangeReasonCode
A coded value specifying why the status has changed.
bridg:ScheduledActivity.statusChangeReasonCode
urn:PSCv2.6:ScheduledActivityState.reason
bridg:ScheduledActivity.statusCode
statusCode
bridg:ScheduledActivity.statusCode
false
bridg:ScheduledActivity.statusCode
A coded value specifying the phase in a lifecycle of a scheduled activity.
bridg:ScheduledActivity.statusCode
For a lab test
bridg:ScheduledActivity.statusCode
this would be the condition or stage in the lifecycle of the test (e.g.
bridg:ScheduledActivity.statusCode
"scheduled"
bridg:ScheduledActivity.statusCode
"canceled"
bridg:ScheduledActivity.statusCode
"performed").
bridg:ScheduledActivity.statusCode
Please refer to the Scheduled Activity Status state transition diagram for further details.
bridg:ScheduledActivity.statusCode
urn:PSC:ScheduledEventState
bridg:ScheduledActivity.statusDate
statusDate
bridg:ScheduledActivity.statusDate
false
bridg:ScheduledActivity.statusDate
The date (and time) on which the status is assigned to the activity.
bridg:ScheduledActivity.statusDate
urn:PSC:ScheduledEventState.canceled
bridg:ScheduledNotification.message
message
bridg:ScheduledNotification.message
false
bridg:ScheduledNotification.message
The actual text scheduled to be included in the notification.
bridg:ScheduledNotification.message
This may mean that message variables have been replaced with actual data.
bridg:ScheduledNotification.message
urn:caAERSv2.2:ScheduledEmailNotification.body
bridg:ScheduledNotification.messageTitle
messageTitle
bridg:ScheduledNotification.messageTitle
false
bridg:ScheduledNotification.messageTitle
The subject of the notification.
bridg:ScheduledNotification.messageTitle
urn:caAERSv2.2:ScheduledEmailNotification.subject
bridg:ScheduledSubstanceAdministration.activeIngredientDose
activeIngredientDose
bridg:ScheduledSubstanceAdministration.activeIngredientDose
false
bridg:ScheduledSubstanceAdministration.activeIngredientDose
The quantity of active ingredient anticipated to be administered.
bridg:ScheduledSubstanceAdministration.activeIngredientDose
5 mg
bridg:ScheduledSubstanceAdministration.activeIngredientDose
This is intended to be a subject-specific quantity.
DefinedSubstanceAdministration.productDose can contain a dose expressed in absolute or relative terms (e.g., mg or mg/kg). ScheduledSubstanceAdministration.activeIngredientDose and PerformedSubstanceAdministration.productDose must contain a dose expressed in absolute terms (e.g., mg). If the DefinedSubstanceAdministration.productDose was expressed in relative terms (e.g., mg/kg), then the absolute dose must have been calculated using one or more observed factors as identified by the DefinedDoseExpressionVariableRelationship.
bridg:Service.typeCode
typeCode
bridg:Service.typeCode
false
bridg:Service.typeCode
A coded value specifying the kind of service.
bridg:Service.typeCode
Institutional Review Board (IRB)
bridg:Service.typeCode
Data Safety Monitoring Board (DSMB)
bridg:Service.typeCode
Data Coordinating Center
bridg:Service.typeCode
urn:C3PR:StudyCoordinatingCenter
bridg:Service.typeCode
urn:C3PR:BookRandomization
bridg:Service.typeCode
urn:CTR_Rr2:Trial_has_data_monitoring_committee
bridg:Service.typeCode
urn:CTRPv3.8:OrganizationFunctionalRole.functionCode
bridg:Service.typeCode
urn:CTRRr3:Service.typeCode
bridg:Service.typeCode
urn:CTRv1.0:Service.typeCode
bridg:Service.typeCode
urn:caAERSv2.2:StudyCoordinatingCenter
bridg:ServiceDeliveryLocation.code
code
bridg:ServiceDeliveryLocation.code
false
bridg:ServiceDeliveryLocation.code
A coded value specifying the kind of service delivery location.
bridg:ServiceDeliveryLocation.code
incidental
bridg:ServiceDeliveryLocation.code
dedicated
bridg:ServiceDeliveryLocation.code
clinical
bridg:ServiceDeliveryLocation.code
non-clinical
bridg:ServiceDeliveryLocation.code
A service delivery location may be either an incidental service delivery location (a place at which services may be provided without prior designation or authorization) or a dedicated service delivery location (a place that is intended to house the provision of services). Dedicated service delivery locations can be further characterized as either clinical or non-clinical.
bridg:ServiceDeliveryLocation.code
urn:CTRv1.0:ServiceDeliveryLocation.code
in R_ServiceDeliveryLocation informational
bridg:ServiceDeliveryLocation.code
urn:ICSRr2:ServiceDeliveryLocation.code
bridg:ServiceDeliveryLocation.postalAddress
postalAddress
bridg:ServiceDeliveryLocation.postalAddress
false
bridg:ServiceDeliveryLocation.postalAddress
A contact point used to send physical forms of communication to the service delivery location.
bridg:ServiceDeliveryLocation.postalAddress
urn:CTRv1.0:ServiceDeliveryLocation.postalAddress
in R_ServiceDeliveryLocation informational
bridg:ServiceDeliveryLocation.postalAddress
urn:ICSRr2:ServiceDeliveryLocation.addr
bridg:ServiceDeliveryLocation.telecomAddress
telecomAddress
bridg:ServiceDeliveryLocation.telecomAddress
false
bridg:ServiceDeliveryLocation.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the service delivery location.
bridg:ServiceDeliveryLocation.telecomAddress
The set of digits that serves as the address for a telephone device. Included in the phone number are country, city, and area codes needed to uniquely address the telephone. A URL or e-mail would be similarly described.
bridg:ServiceDeliveryLocation.telecomAddress
urn:CTRv1.0:ServiceDeliveryLocation.telecomAddress
in R_ServiceDeliveryLocation informational
bridg:ServiceDeliveryLocation.telecomAddress
urn:ICSRr2:ServiceDeliveryLocation.telecom
bridg:Specimen.accessionNumberText
accessionNumberText
bridg:Specimen.accessionNumberText
false
bridg:Specimen.accessionNumberText
An alphanumeric identifier (not necessarily unique to the specimen) assigned by a receiving lab to specimens that are received together as a set.
bridg:Specimen.accessionNumberText
urn:CDASHv1.1:LB.LBREFID
bridg:Specimen.accessionNumberText
urn:CTRv1.0:Specimen.accessionNumberText
bridg:Specimen.accessionNumberText
urn:Lab:Specimen.accessionNumber
bridg:Specimen.accessionNumberText
urn:LabViewer2.2:Specimen.accessionNumber
bridg:Specimen.accessionNumberText
urn:NCI_CRF_Standard:CDE_2230047v4.0:_Specimen_Accession_Number
bridg:Specimen.accessionNumberText
urn:SDTM_IGv3.1.2:LB.LBREFID
bridg:Specimen.conditionCode
conditionCode
bridg:Specimen.conditionCode
true
bridg:Specimen.conditionCode
A coded value specifying one of a discreet list of values describing the condition of the specimen at time of receipt at the lab.
bridg:Specimen.conditionCode
Hemolyzed
bridg:Specimen.conditionCode
Icteric
bridg:Specimen.conditionCode
Lipemic
bridg:Specimen.conditionCode
Derived from PerformedObservationResult.value(ANY=>CD).code WHERE PerformedObservationResult > PerformedObservation > DefinedObservation.nameCode = "assess specimen condition"
bridg:Specimen.conditionCode
urn:CDASHv1.1:LB.LBSPCCND
bridg:Specimen.conditionCode
urn:CTRv1.0:Specimen.conditionCode
bridg:Specimen.conditionCode
urn:Lab:Specimen.condition
bridg:Specimen.conditionCode
urn:LabViewer2.2:Specimen.condition
bridg:Specimen.conditionCode
urn:NCI_CRF_Standard:CDE_2829883v1.0:_Laboratory_Specimen_Condition_Gross_Type
bridg:Specimen.conditionCode
urn:SDTM_IGv3.1.1:LB.LBSPCCND
bridg:Specimen.conditionCode
urn:SDTM_IGv3.1.2:LB.LBSPCCND
bridg:Specimen.conditionCode
urn:SDTM_IGv3.1.2:MB.MBSPCCND
bridg:Specimen.conditionCode
urn:SDTM_IGv3.1.2:PC.PCSPCCND
bridg:Specimen.typeCode
typeCode
bridg:Specimen.typeCode
false
bridg:Specimen.typeCode
A coded value specifying the kind of the specimen derived from other specimens.
bridg:Specimen.typeCode
specimen
bridg:Specimen.typeCode
aliquot
bridg:Specimen.typeCode
isolate
bridg:Specimen.typeCode
urn:CTRv1.0:Specimen.typeCode
in R_Specimen universal
bridg:Specimen.typeCode
urn:ICSRr2:Specimen.code
bridg:StatisticalAnalysisPlanVersion.description
description
bridg:StatisticalAnalysisPlanVersion.description
false
bridg:StatisticalAnalysisPlanVersion.description
The textual explanation of the statistical analysis plan version.
bridg:StatisticalAnalysisPlanVersion.description
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion.description
bridg:StatisticalAnalysisPlanVersion.identifier
identifier
bridg:StatisticalAnalysisPlanVersion.identifier
false
bridg:StatisticalAnalysisPlanVersion.identifier
A unique symbol that establishes the identity of a version of the statistical analysis plan.
bridg:StatisticalAnalysisPlanVersion.identifier
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion.versionIdentifier
bridg:StatisticalAnalysisPlanVersion.typeCode
typeCode
bridg:StatisticalAnalysisPlanVersion.typeCode
false
bridg:StatisticalAnalysisPlanVersion.typeCode
A coded value specifying them kind of statistical analysis plan version.
bridg:StatisticalAnalysisPlanVersion.typeCode
draft
bridg:StatisticalAnalysisPlanVersion.typeCode
approved
bridg:StatisticalAnalysisPlanVersion.typeCode
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion.versionTypeCode
bridg:StatisticalAnalysisPlanVersionModificationSummary.date
date
bridg:StatisticalAnalysisPlanVersionModificationSummary.date
false
bridg:StatisticalAnalysisPlanVersionModificationSummary.date
The date (and time) on which the modification took place.
bridg:StatisticalAnalysisPlanVersionModificationSummary.date
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary.date
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
reasonCode
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
false
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
A coded value specifying the motivation, cause, or rationale for the modification.
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
Request by FDA
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
New information available
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
Change in strategy
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
Error correction
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
Actual analysis differed from planned
bridg:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary.reasonCode
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
text
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
false
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
Textual or media-based summary of the changes.
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
Distribution assumptions for some analyses were not met
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
so additional analyses were performed to check robustness of results.
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
Another drug in the class has been approved so additional analyses of a new exploratory endpoint have been added.
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
Site was non-compliant so additional analyses are needed to handle this site's data.
bridg:StatisticalAnalysisPlanVersionModificationSummary.text
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary.text
bridg:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
timingDescription
bridg:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
false
bridg:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
Text description of when the modification occurred relative to the study.
bridg:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
Modification made prior to unblinding
bridg:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
Modification made prior to first subject's first visit
bridg:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary.timingDescription
bridg:StatisticalAnalysisPlanVersionStatus.code
code
bridg:StatisticalAnalysisPlanVersionStatus.code
false
bridg:StatisticalAnalysisPlanVersionStatus.code
A coded value specifying the phase in the lifecycle of the statistical analysis plan version.
bridg:StatisticalAnalysisPlanVersionStatus.code
active
bridg:StatisticalAnalysisPlanVersionStatus.code
inactive
bridg:StatisticalAnalysisPlanVersionStatus.code
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion.versionStatusCode
bridg:StatisticalAnalysisPlanVersionStatus.date
date
bridg:StatisticalAnalysisPlanVersionStatus.date
false
bridg:StatisticalAnalysisPlanVersionStatus.date
The date that the statistical analysis plan version entered the current status.
bridg:StatisticalAnalysisPlanVersionStatus.date
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion.versionDate
bridg:StratumGroup.description
description
bridg:StratumGroup.description
false
bridg:StratumGroup.description
The textual representation of the stratum group.
bridg:StratumGroup.description
Primary malignancy
bridg:StratumGroup.description
Weight loss severity
bridg:StratumGroup.description
Concurrent therapy
bridg:StratumGroup.description
Patient age (years)
bridg:StratumGroup.description
Gleason score
bridg:StratumGroup.description
Baseline PSA
bridg:StratumGroup.description
urn:CTRPv3.8:StratumGroup.description
bridg:StratumGroup.groupNumber
groupNumber
bridg:StratumGroup.groupNumber
false
bridg:StratumGroup.groupNumber
An integer that identifies the stratum group to study personnel, such as the statistician and registrars.
bridg:StratumGroup.groupNumber
Patient age (years)
bridg:StratumGroup.groupNumber
Stratum A
bridg:StratumGroup.groupNumber
Gender
bridg:StratumGroup.groupNumber
Two-year survival probability
bridg:StratumGroup.groupNumber
Disease Type
bridg:StratumGroup.groupNumber
Treatment Cohort
bridg:StratumGroup.groupNumber
This index is used to cross-reference the stratum group and set of arms during registration. It is provided to perform a lookup in the randomization book or statistical algorithm when performing randomization.
Text is captured using the originalText attribute of the INT.NONNEG data type.
bridg:StratumGroup.groupNumber
urn:C3PR:StratumGroup.stratumGroupNumber
bridg:StratumGroup.groupNumber
urn:C3PRv2.9:StratumGroup.stratumGroupNumber
bridg:StratumGroup.groupNumber
urn:CTRPv1.0:StratumGroup.groupNumberText
bridg:StratumGroup.groupNumber
urn:CTRPv3.8:StratumGroup.groupNumberText
bridg:StratumGroup.groupNumber
urn:CTRRr3:StratumGroup.groupNumber
bridg:StratumGroup.groupNumber
urn:CTRv1.0:StratumGroup.groupNumber
bridg:StudyActivity.studyFocusIndicator
studyFocusIndicator
bridg:StudyActivity.studyFocusIndicator
false
bridg:StudyActivity.studyFocusIndicator
Specifies whether the activity is a key investigational activity for a study.
bridg:StudyActivity.studyFocusIndicator
A study focused on investigating the effectiveness of a drug will flag the substance administration of the drug or a study focused on determining the average blood pressure of a certain population will flag the blood pressure observation.
bridg:StudyActivity.studyFocusIndicator
If a study has study agents, one or more of the study activities will presumably use the agent and have this indicator set to true.
bridg:StudyActivity.studyFocusIndicator
urn:CTRPv1.0:PlannedEligibilityCriterion.name
bridg:StudyActivity.studyFocusIndicator
urn:CTRR:Intervention_Name
s product name(s
bridg:StudyActivity.studyFocusIndicator
urn:CTRR:Comparator
bridg:StudyActivity.studyFocusIndicator
urn:CTRv1.0:StudyActivity.studyFocusIndicator
bridg:StudyAgent.blindedName
blindedName
bridg:StudyAgent.blindedName
false
bridg:StudyAgent.blindedName
A non-unique textual identifier of a study agent to be used by participants from whom the identity of the study agent is hidden. This name is assigned within the context of a study so that products which blinded participants should not be able to distinguish between/among have the same blinded name.
bridg:StudyAgent.blindedName
In a study for which the study agents are a drug product and a matching placebo
bridg:StudyAgent.blindedName
both the active product and the placebo might simply be called "Study Drug."
bridg:StudyAgent.blindedName
In a study with two different investigational products and their matching placebos
bridg:StudyAgent.blindedName
the blinded names might be "Bottle A" and "Bottle B" or "100 mg tablet" and "25 mg tablet."
bridg:StudyAgent.blindedName
urn:GSK_MDRv1.0:GForge__27182_-_Blinded_Description_for_Product_functioning_as_Study_Agent
bridg:StudyAgent.characteristicModifiedIndicator
characteristicModifiedIndicator
bridg:StudyAgent.characteristicModifiedIndicator
false
bridg:StudyAgent.characteristicModifiedIndicator
Specifies whether the agent's characteristic have been modified from those approved in the marketing authorization in a way that could affect its quality.
bridg:StudyAgent.characteristicModifiedIndicator
Modification may include a change in pharmaceutical form (e.g. over-encapsulation, colour, dilution, re-tabletting for blinding etc.) or removal from the primary packaging and repacking (e.g. removal from a blister and putting in a bottle).
bridg:StudyAgent.characteristicModifiedIndicator
urn:CTRRr3:StudyAgent.modifiedIndicator
bridg:StudyAgent.expandedAccessIndicator
expandedAccessIndicator
bridg:StudyAgent.expandedAccessIndicator
false
bridg:StudyAgent.expandedAccessIndicator
Specifies whether the product (drug or device) is available for patients who are not adequately treated by existing therapy, who do not meet the eligibility criteria for enrollment, or who are otherwise unable to participate in a controlled study. Expanded Access is a mechanism that provides non-protocol access to experimental treatments, including protocol exception, single-patient IND, treatment IND, compassionate use, emergency use, continued access and parallel track.
bridg:StudyAgent.expandedAccessIndicator
urn:CTGOV:Has_Expanded_Access
bridg:StudyAgent.expandedAccessIndicator
urn:CTGOV:Study_Type_-_Expanded_Access_and_Has_Expanded_Access?
bridg:StudyAgent.expandedAccessIndicator
urn:CTRPv1.0:StudyProtocol.expandedAccessIndicator
bridg:StudyAgent.expandedAccessIndicator
urn:CTRPv1.0:ObservationalStudyProtocol.expandedAccessIndicator
bridg:StudyAgent.expandedAccessIndicator
urn:CTRPv1.0:InterventionalStudyProtocol.expandedAccessIndicator
bridg:StudyAgent.expandedAccessIndicator
urn:CTRPv3.8:StudyIndIde.expandedAccessIndicator
bridg:StudyAgent.expandedAccessIndicator
urn:CTRR:Expanded_access_indicator
bridg:StudyAgent.expandedAccessIndicator
urn:CTRRr3:StudyAgent.expandedAccessIndicator
bridg:StudyAgent.firstInHumanIndicator
firstInHumanIndicator
bridg:StudyAgent.firstInHumanIndicator
false
bridg:StudyAgent.firstInHumanIndicator
Specifies whether this is the first time an active substance of the agent is to be administered to humans in a study.
bridg:StudyAgent.firstInHumanIndicator
urn:CTRRr3:StudyAgent.firstInHumanIndicator
bridg:StudyAgent.firstInHumanIndicator
urn:CTRRr3:Study.typeCode
bridg:StudyAgent.firstInHumanRiskFactorCode
firstInHumanRiskFactorCode
bridg:StudyAgent.firstInHumanRiskFactorCode
false
bridg:StudyAgent.firstInHumanRiskFactorCode
A coded value specifying the risk factors identified with administering the agent's active substance to humans for the first time in a study.
bridg:StudyAgent.firstInHumanRiskFactorCode
urn:CTRRr3:StudyAgent.firstInHumanRiskFactor
bridg:StudyAgent.functionCode
functionCode
bridg:StudyAgent.functionCode
false
bridg:StudyAgent.functionCode
A coded value specifying how this agent is used in the study.
bridg:StudyAgent.functionCode
lead agent
bridg:StudyAgent.functionCode
comparator agent
bridg:StudyAgent.functionCode
placebo
bridg:StudyAgent.functionCode
active control
bridg:StudyAgent.functionCode
This is important to know in multi-agent studies.
bridg:StudyAgent.functionCode
urn:CTOM:StudyAgent.investigationalIndicator
bridg:StudyAgent.functionCode
urn:CTR_Rr2:IMP_Category
bridg:StudyAgent.functionCode
urn:CTRPv1.0:StudyProduct.leadProductIndicator
bridg:StudyAgent.functionCode
urn:CTRR:Comparator_Description
bridg:StudyAgent.functionCode
urn:CTRRr3:StudyAgent.functionCode
bridg:StudyAgent.functionCode
urn:CTRv1.0:StudyAgent.functionCode
bridg:StudyAgent.functionCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_COMPTRT
bridg:StudyAgent.functionCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_TRT
bridg:StudyAgent.pediatricFormulationIndicator
pediatricFormulationIndicator
bridg:StudyAgent.pediatricFormulationIndicator
false
bridg:StudyAgent.pediatricFormulationIndicator
Specifies whether the pharmaceutical form of the agent is intended for pediatric usage.
bridg:StudyAgent.pediatricFormulationIndicator
A value of true may indicate that the agent is dissolvable
bridg:StudyAgent.pediatricFormulationIndicator
smaller
bridg:StudyAgent.pediatricFormulationIndicator
or grape flavored to be easily ingested by the pediatric population.
bridg:StudyAgent.pediatricFormulationIndicator
urn:CTRRr3:DefinedActivity.subcategoryCode
bridg:StudyAgent.pediatricFormulationIndicator
urn:CTRRr3:DefinedActivity.categoryCode
bridg:StudyAgent.statusCode
statusCode
bridg:StudyAgent.statusCode
false
bridg:StudyAgent.statusCode
A coded value specifying the phase in the lifecycle of the agent's association to a study.
bridg:StudyAgent.statusCode
pending
bridg:StudyAgent.statusCode
active
bridg:StudyAgent.statusCode
complete
bridg:StudyAgent.statusCode
cancelled
bridg:StudyAgent.statusCode
urn:CTOM:StudyAgent.statusCode
bridg:StudyAgent.statusCode
urn:CTRPv1.0:StudyProduct.statusCode
bridg:StudyAgent.statusCode
urn:CTRv1.0:StudyAgent.statusCode
bridg:StudyAgent.statusDate
statusDate
bridg:StudyAgent.statusDate
false
bridg:StudyAgent.statusDate
The date (and time) on which the status is assigned to the study agent.
bridg:StudyAgent.statusDate
urn:CTOM:StudyAgent.statusDate
bridg:StudyAgent.statusDate
urn:CTRPv1.0:StudyProduct.statusDateRange
bridg:StudyAgent.statusDate
urn:CTRv1.0:StudyAgent.statusDate
bridg:StudyAgent.substitutionAllowedIndicator
substitutionAllowedIndicator
bridg:StudyAgent.substitutionAllowedIndicator
false
bridg:StudyAgent.substitutionAllowedIndicator
Specifies whether this agent as identified by its active substance is permitted to be substituted by a local brand.
bridg:StudyAgent.substitutionAllowedIndicator
The study protocol may specify the use of Paracetamol which could be substituted locally in the United States with any brand containing acetaminophen
bridg:StudyAgent.substitutionAllowedIndicator
including Tylenol and Panadol.
bridg:StudyAgent.substitutionAllowedIndicator
urn:CTRRr3:StudyAgent.substitutionAllowedCode
bridg:StudyCondition.code
code
bridg:StudyCondition.code
false
bridg:StudyCondition.code
A coded value specifying the condition that is the focus of the study.
bridg:StudyCondition.code
In a study to examine risk factors for Lupus
bridg:StudyCondition.code
might have as an inclusion criterion "healthy volunteer"
bridg:StudyCondition.code
but the target condition code would be a Lupus SNOMED code.
bridg:StudyCondition.code
urn:C3PRv2.9:DiseaseTerm.ctepTerm
bridg:StudyCondition.code
urn:C3PRv2.9:DiseaseTerm.medraCode
bridg:StudyCondition.code
urn:C3PRv2.9:DiseaseTerm.term
bridg:StudyCondition.code
urn:C3PRv2.9:DiseaseTerm
bridg:StudyCondition.code
urn:CTOM:Protocol.diseaseCode
bridg:StudyCondition.code
urn:CTR_Rr2:MedDRA_Code
bridg:StudyCondition.code
urn:CTR_Rr2:Medical_condition
bridg:StudyCondition.code
urn:CTR_Rr2:Medical_condition_in_lay_language
bridg:StudyCondition.code
urn:CTR_Rr2:MedDRA_Level
bridg:StudyCondition.code
urn:CTR_Rr2:MedDRA_Version
bridg:StudyCondition.code
urn:CTR_Rr2:MedDRA_Term
bridg:StudyCondition.code
urn:CTR_Rr2:MedDRA_EUTCT_ID
bridg:StudyCondition.code
urn:CTRPv1.0:InterventionalStudyProtocol.diseaseCode
bridg:StudyCondition.code
urn:CTRPv1.0:ObservationalStudyProtocol.diseaseCode
bridg:StudyCondition.code
urn:CTRPv1.0:StudyProtocol.diseaseCode
bridg:StudyCondition.code
urn:CTRPv3.8:StudyDisease.diseaseCode
bridg:StudyCondition.code
urn:CTRRr3:Study.diseaseCode
bridg:StudyCondition.code
urn:CTRv1.0:StudyCondition.code
bridg:StudyCondition.code
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_INDIC
bridg:StudyCondition.code
urn:caAERSv2.2:DiseaseTerm.ctepTerm
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.whoArtCode
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.jartCode
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.version_id
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.meddraCode___MeddraStudyDisease
bridg:StudyCondition.code
urn:caAERSv2.2:Condition.name
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.icd10Code
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.hartsCode
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.meddraTerm
bridg:StudyCondition.code
urn:caAERSv2.2:DiseaseTerm.term
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.costartSymbol
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.icd9CmCode
bridg:StudyCondition.code
urn:caAERSv2.2:DiseaseTerm.medraCode
bridg:StudyCondition.code
urn:caAERSv2.2:AbstractMeddraDomain.icd9Code
bridg:StudyCondition.code
urn:caAERSv2.2:MeddraVersion.name___MeddraStudyDisease
bridg:StudyCondition.leadIndicator
leadIndicator
bridg:StudyCondition.leadIndicator
false
bridg:StudyCondition.leadIndicator
Specifies whether this is the primary condition of a study.
bridg:StudyCondition.leadIndicator
urn:C3PRv2.9:StudyDisease.leadDisease
bridg:StudyCondition.leadIndicator
urn:CTRPv3.8:StudyDisease.leadDiseaseIndicator
bridg:StudyCondition.leadIndicator
urn:CTRv1.0:StudyCondition.leadIndicator
bridg:StudyCondition.leadIndicator
urn:caAERSv2.2:AbstractStudyDisease.leadDisease
bridg:StudyExecution.effectiveDateRange
effectiveDateRange
bridg:StudyExecution.effectiveDateRange
true
bridg:StudyExecution.effectiveDateRange
Specifies the period of time over which the study was executed
bridg:StudyExecution.effectiveDateRange
May specify the start and/or end or duration. This can be derived by looking at the StudyOverallStatus where low.value corresponds to the activation date and high.value corresponds to the completion date.
bridg:StudyExecution.effectiveDateRange
urn:CTRv1.0:StudyExecution.effectiveDateRange
bridg:StudyExecution.enrolledStudySubjectNumber
enrolledStudySubjectNumber
bridg:StudyExecution.enrolledStudySubjectNumber
true
bridg:StudyExecution.enrolledStudySubjectNumber
An integer specifying the quantity of study subjects enrolled in the study at the current time.
bridg:StudyExecution.enrolledStudySubjectNumber
This can be derived by counting the number of enrolled subjects.
bridg:StudyExecution.enrolledStudySubjectNumber
urn:CTRv1.0:StudyRecruitmentStatus.enrolledSubjectNumber
bridg:StudyInvestigator.identifier
identifier
bridg:StudyInvestigator.identifier
false
bridg:StudyInvestigator.identifier
A unique symbol that establishes identity of the study investigator.
bridg:StudyInvestigator.identifier
urn:C3PR:Investigator.nciIdentifier
bridg:StudyInvestigator.identifier
urn:CDASHv1.1:DM.INVID
bridg:StudyInvestigator.identifier
urn:CTRPv1.0:StudyInvestigator.id
bridg:StudyInvestigator.identifier
urn:CTRv1.0:StudyInvestigator.identifier
bridg:StudyInvestigator.identifier
urn:HL7SP:Investigator.id
bridg:StudyInvestigator.identifier
urn:SDTM_IGv3.1.1:DM.INVID
bridg:StudyInvestigator.identifier
urn:SDTM_IGv3.1.2:DM.INVID
bridg:StudyInvestigator.signatureText
signatureText
bridg:StudyInvestigator.signatureText
false
bridg:StudyInvestigator.signatureText
The signed name of the investigator who is responsible for completing a form or report for a clinical study.
bridg:StudyInvestigator.signatureText
A textual or multimedia depiction of the signature by which the participant endorses his or her participation in the activity as a specified role and that he or she agrees to assume the associated accountability.
bridg:StudyInvestigator.signatureText
urn:C3PR:StudyInvestigator.signatureText
bridg:StudyInvestigator.signatureText
urn:C3PR:StudyInvestigator.signatureIndicator
bridg:StudyInvestigator.signatureText
urn:CTOM:StudyInvestigator.signatureIndicator
bridg:StudyInvestigator.signatureText
urn:CTOM:StudyInvestigator.signatureText
bridg:StudyInvestigator.signatureText
urn:CTRPv1.0:StudyInvestigator.signatureText
bridg:StudyInvestigator.signatureText
urn:CTRv1.0:StudyInvestigator.signatureText
bridg:StudyInvestigator.signatureText
urn:NCI_CRF_Standard:CDE_58320v5.0:_Investigator_Signature_Text
bridg:StudyInvestigator.signatureText
urn:caAERSv2.2:StudyInvestigator.signatureText
bridg:StudyLegalSponsor.primaryIndicator
primaryIndicator
bridg:StudyLegalSponsor.primaryIndicator
false
bridg:StudyLegalSponsor.primaryIndicator
Specifies whether this is the main or principal study legal sponsor.
bridg:StudyLegalSponsor.primaryIndicator
urn:CTRR:Sponsor
bridg:StudyLegalSponsor.primaryIndicator
urn:CTRv1.0:StudyLegalSponsor.primaryIndicator
bridg:StudyLegalSponsor.primaryIndicator
urn:WHO:Secondary_Sponsor
bridg:StudyLegalSponsor.primaryIndicator
urn:WHO:Primary_Sponsor
bridg:StudyObjective.description
description
bridg:StudyObjective.description
false
bridg:StudyObjective.description
The textual representation of the study objective.
bridg:StudyObjective.description
The objective of the analysis is to evaluate the efficacy of study treatment versus placebo. The Alzheimer's Disease Assessment Scale - Cognitive Subscale
bridg:StudyObjective.description
total of 11 items [ADAS-Cog (11)] and the Video-referenced Clinician's Interview-based Impression of Change (CIBIC+) will serve as the primary efficacy instruments. Efficacy will be determined by testing for a statistically significant relationship between the change in both the ADAS-Cog (11) and CIBIC+ scores
bridg:StudyObjective.description
and drug dose (0
bridg:StudyObjective.description
low dose [54 mg]
bridg:StudyObjective.description
and high dose [81 mg]).
bridg:StudyObjective.description
The example above makes reference to content from more than just the StudyObjective class, rather also from classes closely related to it. However, in prose presentation, this is common practice. See BRIDG GForge Tracker #30649 and #31401.
bridg:StudyObjective.description
urn:CTR_Rr2:Trial_secondary_objective
bridg:StudyObjective.description
urn:CTR_Rr2:Trial_main_objective
bridg:StudyObjective.description
urn:CTRPv3.8:StudyObjective.outline
bridg:StudyObjective.description
urn:CTRRr3:StudyObjective.description
bridg:StudyObjective.description
urn:CTRv1.0:StudyObjective.description
bridg:StudyObjective.description
urn:HSDBv1.0:[Study].Primary_Purpose
bridg:StudyObjective.description
urn:HSDBv1.0:[Study].Primary_Purpose_'Other'_value_specification
bridg:StudyObjective.description
urn:SDTM_IGv3.1.1:TS.TSPARMCD
bridg:StudyObjective.description
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_OBJSEC
bridg:StudyObjective.description
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_OBJPRIM
bridg:StudyObjective.typeCode
typeCode
bridg:StudyObjective.typeCode
false
bridg:StudyObjective.typeCode
A coded value specifying the kind of study objective.
bridg:StudyObjective.typeCode
primary
bridg:StudyObjective.typeCode
secondary
bridg:StudyObjective.typeCode
tertiary
bridg:StudyObjective.typeCode
exploratory
bridg:StudyObjective.typeCode
The examples given are the only allowable concepts for this attribute.
bridg:StudyObjective.typeCode
urn:SDTM_IGv3.1.1:TS.TSPARMCD
bridg:StudyOutcomeMeasure.description
description
bridg:StudyOutcomeMeasure.description
false
bridg:StudyOutcomeMeasure.description
The textual summary of the study outcome measure used to clarify its meaning, method, or purpose.
bridg:StudyOutcomeMeasure.description
urn:CTRPv3.8:StudyOutcomeMeasure.descriptionText
bridg:StudyOutcomeMeasure.description
urn:CTRRr3:StudyOutcomeMeasure.description
bridg:StudyOutcomeMeasure.name
name
bridg:StudyOutcomeMeasure.name
false
bridg:StudyOutcomeMeasure.name
A non-unique textual identifier for the study outcome measure.
bridg:StudyOutcomeMeasure.name
all-cause mortality
bridg:StudyOutcomeMeasure.name
urn:CTGOV:Outcome_Measure
bridg:StudyOutcomeMeasure.name
urn:CTGOV:Secondary_Outcome_Measure
bridg:StudyOutcomeMeasure.name
urn:CTR_Rr2:Primary_end_points
bridg:StudyOutcomeMeasure.name
urn:CTR_Rr2:Secondary_end_point
bridg:StudyOutcomeMeasure.name
urn:CTRPv1.0:StudyOutcomeMeasure.name
bridg:StudyOutcomeMeasure.name
urn:CTRPv3.8:StudyObjective.name
bridg:StudyOutcomeMeasure.name
urn:CTRPv3.8:StudyOutcomeMeasure.name
bridg:StudyOutcomeMeasure.name
urn:CTRR:Outcomes
bridg:StudyOutcomeMeasure.name
urn:CTRRr3:StudyOutcomeMeasure.name
bridg:StudyOutcomeMeasure.name
urn:CTRv1.0:StudyOutcomeMeasure.name
bridg:StudyOutcomeMeasure.primaryIndicator
primaryIndicator
bridg:StudyOutcomeMeasure.primaryIndicator
false
bridg:StudyOutcomeMeasure.primaryIndicator
Specifies whether this is the main or principal study outcome measure.
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTGOV:Primary_Outcome_Measure
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTRPv1.0:StudyOutcomeMeasure.primaryIndicator
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTRPv3.8:StudyOutcomeMeasure.primaryIndicator
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTRR:Outcomes
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTRR:Primary_Outcome_Type
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTRRr3:StudyOutcomeMeasure.primaryIndicator
bridg:StudyOutcomeMeasure.primaryIndicator
urn:CTRv1.0:StudyOutcomeMeasure.primaryIndicator
bridg:StudyOutcomeMeasure.timeFrameText
timeFrameText
bridg:StudyOutcomeMeasure.timeFrameText
false
bridg:StudyOutcomeMeasure.timeFrameText
Time point(s) at which the study outcome measure is assessed
bridg:StudyOutcomeMeasure.timeFrameText
one year
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTGOV:Time_Frame
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTR_Rr2:Secondary_end_point_timepoint
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTR_Rr2:Primary_end_point_timepoint
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTRPv1.0:StudyOutcomeMeasure.timeframe
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTRPv3.8:StudyOutcomeMeasure.timeFrame
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTRR:Outcomes
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTRRr3:StudyOutcomeMeasure.timeFrameText
bridg:StudyOutcomeMeasure.timeFrameText
urn:CTRv1.0:StudyOutcomeMeasure.timeFrameText
bridg:StudyOutcomeMeasure.typeCode
typeCode
bridg:StudyOutcomeMeasure.typeCode
false
bridg:StudyOutcomeMeasure.typeCode
A coded value specifying the kind of study outcome measure.
bridg:StudyOutcomeMeasure.typeCode
n/a
bridg:StudyOutcomeMeasure.typeCode
safety
bridg:StudyOutcomeMeasure.typeCode
efficacy
bridg:StudyOutcomeMeasure.typeCode
bio-equivalence
bridg:StudyOutcomeMeasure.typeCode
bio-availability
bridg:StudyOutcomeMeasure.typeCode
pharmacokinetics
bridg:StudyOutcomeMeasure.typeCode
pharmacodynamics
bridg:StudyOutcomeMeasure.typeCode
urn:CTGOV:Safety_Issue?
bridg:StudyOutcomeMeasure.typeCode
urn:CTGOV:Study_Classification
bridg:StudyOutcomeMeasure.typeCode
urn:CTOM:Trial_scope_Pharmacokinetics
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Prophylaxis
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Diagnosis
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Other
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Therapy
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Efficacy
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Dose_response
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Bioequivalence
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Pharmacogenetic
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Pharmacodynamics
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Safety
bridg:StudyOutcomeMeasure.typeCode
urn:CTR_Rr2:Trial_scope_Other_specification
bridg:StudyOutcomeMeasure.typeCode
urn:CTRPv1.0:StudyOutcomeMeasure.typeCode
bridg:StudyOutcomeMeasure.typeCode
urn:CTRPv3.8:InterventionalStudyProtocol.studyClassificationCode
bridg:StudyOutcomeMeasure.typeCode
urn:CTRR:Primary_Outcome_Type
bridg:StudyOutcomeMeasure.typeCode
urn:CTRRr3:StudyOutcomeMeasure.typeCode
bridg:StudyOutcomeMeasure.typeCode
urn:CTRv1.0:StudyOutcomeMeasure.typeCode
bridg:StudyOutcomeMeasure.typeCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_TTYPE
bridg:StudyOverallStatus.anticipatedIndicator
anticipatedIndicator
bridg:StudyOverallStatus.anticipatedIndicator
false
bridg:StudyOverallStatus.anticipatedIndicator
Specifies whether the overall status of the study is an estimate.
bridg:StudyOverallStatus.anticipatedIndicator
BRIDG SCC has made the decision to add an anticipatedIndicator until we learn the business rules of how the overall study status could be derived.
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:InterventionalStudyProtocol.startDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:StudyProtocol.primaryCompletionDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:ObservationalStudyProtocol.primaryCompletionDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:ObservationalStudyProtocol.startDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:StudyProtocol.startDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:InterventionalStudyProtocol.primaryCompletionDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv1.0:StudyOverallStatus.anticipatedIndicator
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv3.8:StudyOverallStatus.statusTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv3.8:StudyProtocol.startDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRPv3.8:StudyProtocol.primaryCompletionDateTypeCode
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRR:Completion_date__estimated_or_actual
estimated or actual
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRR:Primary_Completion_Date
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRRr3:StudyOverallStatus.anticipatedIndicator
bridg:StudyOverallStatus.anticipatedIndicator
urn:CTRv1.0:StudyOverallStatus.anticipatedIndicator
bridg:StudyOverallStatus.anticipatedIndicator
urn:HSDBv1.0:[Study_status]_.Study_Start_Date_Type
bridg:StudyOverallStatus.anticipatedIndicator
urn:HSDBv1.0:[Study_status]_.Primary_Completion_Date_Type
bridg:StudyOverallStatus.code
code
bridg:StudyOverallStatus.code
false
bridg:StudyOverallStatus.code
A coded value specifying the phase in the lifecycle of the study as a whole.
bridg:StudyOverallStatus.code
In Review
bridg:StudyOverallStatus.code
Approved
bridg:StudyOverallStatus.code
Active
bridg:StudyOverallStatus.code
Closed to Accrual
bridg:StudyOverallStatus.code
Closed to Accrual and Intervention
bridg:StudyOverallStatus.code
Temporary Closed to Accrual
bridg:StudyOverallStatus.code
Temporary Closed to Accrual and Intervention
bridg:StudyOverallStatus.code
Disapproved
bridg:StudyOverallStatus.code
Withdrawn
bridg:StudyOverallStatus.code
Administratively complete.
bridg:StudyOverallStatus.code
Please refer to the Study Overall Status state transition diagram for further details.
The overall status of a study may overlap with the study site status and accrual status. This overlap needs to be clearly differentiated. (See tracker issue 29398). A proposed solution is to eliminate the study recruitmentl status codes and adopt the CTRP values for study status code.
bridg:StudyOverallStatus.code
urn:C3PRv2.9:Study.coordinatingCenterStudyStatus
bridg:StudyOverallStatus.code
urn:CTRPv1.0:StudyOverallStatus.statusCode
bridg:StudyOverallStatus.code
urn:CTRPv3.8:StudyOverallStatus.statusCode
bridg:StudyOverallStatus.code
urn:CTRR:Trial_Status
bridg:StudyOverallStatus.code
urn:CTRRr3:StudyOverallStatus.statusCode
bridg:StudyOverallStatus.code
urn:CTRv1.0:StudyOverallStatus.code
bridg:StudyOverallStatus.code
urn:HSDBv1.0:[Study_status]_.Current_Trial_Status
bridg:StudyOverallStatus.code
urn:caAERSv2.2:Study.status
bridg:StudyOverallStatus.comment
comment
bridg:StudyOverallStatus.comment
false
bridg:StudyOverallStatus.comment
Additional description of the overall status of the study.
bridg:StudyOverallStatus.comment
urn:CTRPv1.0:StudyOverallStatus.commentText
bridg:StudyOverallStatus.comment
urn:CTRPv3.8:StudyOverallStatus.commentText
bridg:StudyOverallStatus.comment
urn:CTRRr3:StudyOverallStatus.comment
bridg:StudyOverallStatus.comment
urn:CTRv1.0:StudyOverallStatus.comment
bridg:StudyOverallStatus.date
date
bridg:StudyOverallStatus.date
false
bridg:StudyOverallStatus.date
The date (and time) on which the overall status of the study is assigned.
bridg:StudyOverallStatus.date
urn:CTGOV:Actual_Study_Completion_Date
bridg:StudyOverallStatus.date
urn:CTGOV:Anticipated_Study_Completion_Date
bridg:StudyOverallStatus.date
urn:CTGOV:Actual_Primary_Completion_Date
bridg:StudyOverallStatus.date
urn:CTGOV:Study_Start_Date
bridg:StudyOverallStatus.date
urn:CTGOV:Anticipated_Primary_Completion_Date
bridg:StudyOverallStatus.date
urn:CTRPv1.0:InterventionalStudyProtocol.statusDate
bridg:StudyOverallStatus.date
urn:CTRPv1.0:StudyProtocol.primaryCompletionDate
bridg:StudyOverallStatus.date
urn:CTRPv1.0:ObservationalStudyProtocol.startDate
bridg:StudyOverallStatus.date
urn:CTRPv1.0:StudyProtocol.startDate
bridg:StudyOverallStatus.date
urn:CTRPv1.0:StudyOverallStatus.statusDate
bridg:StudyOverallStatus.date
urn:CTRPv1.0:InterventionalStudyProtocol.primaryCompletionDate
bridg:StudyOverallStatus.date
urn:CTRPv1.0:ObservationalStudyProtocol.primaryCompletionDate
bridg:StudyOverallStatus.date
urn:CTRPv3.8:StudyOverallStatus.statusDate
bridg:StudyOverallStatus.date
urn:CTRPv3.8:StudyProtocol.primaryCompletionDate
bridg:StudyOverallStatus.date
urn:CTRPv3.8:StudyProtocol.startDate
estimated or actual
bridg:StudyOverallStatus.date
urn:CTRR:Primary_Completion_Date
bridg:StudyOverallStatus.date
urn:CTRR:Completion_date__estimated_or_actual
bridg:StudyOverallStatus.date
urn:CTRRr3:StudyOverallStatus.statusDate
bridg:StudyOverallStatus.date
urn:CTRv1.0:StudyOverallStatus.date
bridg:StudyOverallStatus.date
urn:HSDBv1.0:[Study_status]_.Current_Trial_Status_Date
bridg:StudyOverallStatus.date
urn:HSDBv1.0:[Study_status]_.temporary_closure_start_date
bridg:StudyOverallStatus.date
urn:HSDBv1.0:[Study_status]_.Study_Start_Date
bridg:StudyOverallStatus.date
urn:HSDBv1.0:[Study_status]_.Primary_Completion_Date
bridg:StudyOverallStatus.studyStoppedReasonCode
studyStoppedReasonCode
bridg:StudyOverallStatus.studyStoppedReasonCode
false
bridg:StudyOverallStatus.studyStoppedReasonCode
A coded value specifying why the study has been halted or terminated (for suspended, terminated or withdrawn studies).
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:CTGOV:Why_Study_Stopped
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:CTRPv1.0:StudyOverallStatus.studyStoppedReasonCode
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:CTRPv3.8:StudyOverallStatus.studyStoppedReasonCode
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:CTRRr3:StudyOverallStatus.studyStoppedReasonCode
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:CTRv1.0:StudyOverallStatus.studyStoppedReasonCode
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:HSDBv1.0:[Study_status]_.temporary_closure_status
bridg:StudyOverallStatus.studyStoppedReasonCode
urn:HSDBv1.0:[Study_status]_.Why_Study_Stopped?
bridg:StudyPersonnel.effectiveDateRange
effectiveDateRange
bridg:StudyPersonnel.effectiveDateRange
false
bridg:StudyPersonnel.effectiveDateRange
The date and time span for when the study personnel is active.
bridg:StudyPersonnel.effectiveDateRange
urn:C3PR:StudyInvestigator.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:C3PRv2.9:StudyInvestigator.statusDate
bridg:StudyPersonnel.effectiveDateRange
urn:C3PRv2.9:StudyPersonnel.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:C3PRv2.9:StudyInvestigator.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:C3PRv2.9:StudyPersonnel.statusDate
bridg:StudyPersonnel.effectiveDateRange
urn:CTOM:StudyInvestigator.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:CTRPv1.0:StudyInvestigator.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:CTRPv1.0:StudyInvestigator.statusDateRange
bridg:StudyPersonnel.effectiveDateRange
urn:CTRPv1.0:StudyContact.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:CTRPv1.0:StudyContact.statusDateRange
bridg:StudyPersonnel.effectiveDateRange
urn:CTRPv3.8:FunctionalRole.statusDateRange
bridg:StudyPersonnel.effectiveDateRange
urn:CTRv1.0:StudyPersonnel.effectiveDateRange
bridg:StudyPersonnel.effectiveDateRange
urn:HL7SP:Investigator.statusCode
bridg:StudyPersonnel.effectiveDateRange
urn:caAERSv2.2:StudyInvestigator.startDate
bridg:StudyPersonnel.effectiveDateRange
urn:caAERSv2.2:StudyInvestigator.endDate
bridg:StudyPersonnel.postalAddress
postalAddress
bridg:StudyPersonnel.postalAddress
false
bridg:StudyPersonnel.postalAddress
A contact point used to send physical forms of communication to the study personnel.
bridg:StudyPersonnel.postalAddress
urn:CTGOV:Responsible_Party_-_Contact_Information
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Further_information_contact_Town/City
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Contact_point_for_further_information_on_the_trial_Street_Address
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Investigator_Street_Address
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Investigator_Town/City
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Investigator_Post_Code
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Further_information_contact_Country
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Investigator_Country
bridg:StudyPersonnel.postalAddress
urn:CTR_Rr2:Further_information_contact_Post_Code
bridg:StudyPersonnel.postalAddress
urn:CTRPv1.0:StudyInvestigator.postalAddress
bridg:StudyPersonnel.postalAddress
urn:CTRPv1.0:StudyContact.postalAddress
bridg:StudyPersonnel.postalAddress
urn:CTRPv3.8:StudyContact.postalAddress
bridg:StudyPersonnel.postalAddress
urn:CTRR:Responsible_Contact_Person
bridg:StudyPersonnel.postalAddress
urn:CTRRr3:StudyColleague.postalAddress
bridg:StudyPersonnel.postalAddress
urn:CTRv1.0:StudyPersonnel.postalAddress
bridg:StudyPersonnel.postalAddress
urn:HSDBv1.0:[Principal_Investigator]_.Zip/Postal_code
bridg:StudyPersonnel.postalAddress
urn:HSDBv1.0:[Principal_Investigator]_.Street_Address
bridg:StudyPersonnel.postalAddress
urn:HSDBv1.0:[Principal_Investigator]_.State/Province
bridg:StudyPersonnel.postalAddress
urn:HSDBv1.0:[Principal_Investigator]_.Country
bridg:StudyPersonnel.postalAddress
urn:HSDBv1.0:[Principal_Investigator]_.City
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Scientific_Queries_-_zip
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Public_Queries_-_country
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Public_Queries_-_zip
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Scientific_Queries_-_address
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Public_Queries_-_city
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Scientific_Queries_-_country
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Scientific_Queries_-_city
bridg:StudyPersonnel.postalAddress
urn:WHO:Contact_for_Public_Queries_-_address
bridg:StudyPersonnel.primaryIndicator
primaryIndicator
bridg:StudyPersonnel.primaryIndicator
false
bridg:StudyPersonnel.primaryIndicator
Specifies whether this is the main or principal study personnel.
bridg:StudyPersonnel.primaryIndicator
roleCode and primaryIndicator are redundant attributes when roleCode = "Principal Investigator" and primaryIndicator ="true".
bridg:StudyPersonnel.primaryIndicator
urn:CTRPv1.0:StudyInvestigator.primaryIndicator
bridg:StudyPersonnel.primaryIndicator
urn:CTRPv1.0:StudyContact.primaryIndicator
bridg:StudyPersonnel.primaryIndicator
urn:CTRv1.0:StudyPersonnel.primaryIndicator
bridg:StudyPersonnel.roleCode
roleCode
bridg:StudyPersonnel.roleCode
false
bridg:StudyPersonnel.roleCode
A coded value specifying the type of responsibility of the study personnel.
bridg:StudyPersonnel.roleCode
Study Principal Investigator
bridg:StudyPersonnel.roleCode
Coordinating Investigator
bridg:StudyPersonnel.roleCode
Study Director
bridg:StudyPersonnel.roleCode
Study Chair
bridg:StudyPersonnel.roleCode
Public Queries
bridg:StudyPersonnel.roleCode
Scientific Queries
bridg:StudyPersonnel.roleCode
Scientific Leadership
bridg:StudyPersonnel.roleCode
Registrar
bridg:StudyPersonnel.roleCode
Study Coordinator.
bridg:StudyPersonnel.roleCode
roleCode and primaryIndicator are redundant attributes when roleCode = "Principal Investigator" and primaryIndicator ="true".
bridg:StudyPersonnel.roleCode
urn:C3PR:StudyPersonnel.roleCode
bridg:StudyPersonnel.roleCode
urn:C3PR:StudyInvestigator.roleCode
bridg:StudyPersonnel.roleCode
urn:C3PRv2.9:StudyPersonnel.roleCode
bridg:StudyPersonnel.roleCode
urn:C3PRv2.9:RoleBasedRecipient.role
bridg:StudyPersonnel.roleCode
urn:C3PRv2.9:StudyInvestigator.roleCode
bridg:StudyPersonnel.roleCode
urn:CTGOV:Overall_Study_Officials
bridg:StudyPersonnel.roleCode
urn:CTGOV:Central_Contact_Backup
bridg:StudyPersonnel.roleCode
urn:CTGOV:Central_Contact
bridg:StudyPersonnel.roleCode
urn:CTGOV:Overall_Study_Officials_-_Official's_Role
bridg:StudyPersonnel.roleCode
urn:CTOM:StudyInvestigator.responsibilityRoleCode
bridg:StudyPersonnel.roleCode
urn:CTR_Rr2:Further_information_contact_name
bridg:StudyPersonnel.roleCode
urn:CTRPv1.0:StudyContact.roleCode
bridg:StudyPersonnel.roleCode
urn:CTRPv1.0:StudyInvestigator.roleCode
bridg:StudyPersonnel.roleCode
urn:CTRPv3.8:StudyContact.roleCode
bridg:StudyPersonnel.roleCode
urn:CTRR:Responsible_Contact_Person
bridg:StudyPersonnel.roleCode
urn:CTRRr3:StudyColleague.roleCode
bridg:StudyPersonnel.roleCode
urn:CTRv1.0:StudyPersonnel.roleCode
bridg:StudyPersonnel.roleCode
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/performer.functionCode
bridg:StudyPersonnel.roleCode
urn:HL7SP:Investigator.code
bridg:StudyPersonnel.roleCode
urn:HSDBv1.0:[IND/IDE]_.Holder_Type
bridg:StudyPersonnel.roleCode
urn:WHO:Contact_for_Scientific_Queries_-_type
bridg:StudyPersonnel.roleCode
urn:WHO:Contact_for_Public_Queries_-_type
bridg:StudyPersonnel.roleCode
urn:WHO:Contact_for_Public_Queries
bridg:StudyPersonnel.roleCode
urn:WHO:Contact_for_Scientific_Queries
bridg:StudyPersonnel.roleCode
urn:caAERSv2.2:StudyInvestigator.roleCode
bridg:StudyPersonnel.roleCode
urn:caAERSv2.2:RoleBasedRecipient.role
bridg:StudyPersonnel.telecomAddress
telecomAddress
bridg:StudyPersonnel.telecomAddress
false
bridg:StudyPersonnel.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of the study personnel.
bridg:StudyPersonnel.telecomAddress
urn:CTGOV:Central_Contact_-_Ext
bridg:StudyPersonnel.telecomAddress
urn:CTGOV:Responsible_Party_-_Contact_Information
bridg:StudyPersonnel.telecomAddress
urn:CTGOV:Central_Contact_-_Email
bridg:StudyPersonnel.telecomAddress
urn:CTGOV:Central_Contact_-_Phone
bridg:StudyPersonnel.telecomAddress
urn:CTR_Rr2:Investigator_Telephone
bridg:StudyPersonnel.telecomAddress
urn:CTR_Rr2:Further_information_contact_E-mail
bridg:StudyPersonnel.telecomAddress
urn:CTR_Rr2:Further_information_contact_Telephone
bridg:StudyPersonnel.telecomAddress
urn:CTR_Rr2:Investigator_Email
bridg:StudyPersonnel.telecomAddress
urn:CTR_Rr2:Further_information_contact_Fax
bridg:StudyPersonnel.telecomAddress
urn:CTR_Rr2:Investigator_Fax
bridg:StudyPersonnel.telecomAddress
urn:CTRPv1.0:StudyInvestigator.telecomAddress
bridg:StudyPersonnel.telecomAddress
urn:CTRPv1.0:StudyContact.telecomAddress
bridg:StudyPersonnel.telecomAddress
urn:CTRPv3.8:StudyContact.telecomAddress
bridg:StudyPersonnel.telecomAddress
urn:CTRR:Responsible_Contact_Person
bridg:StudyPersonnel.telecomAddress
urn:CTRRr3:StudyColleague.telecomAddress
bridg:StudyPersonnel.telecomAddress
urn:CTRv1.0:StudyPersonnel.telecomAddress
bridg:StudyPersonnel.telecomAddress
urn:HSDBv1.0:[Principal_Investigator]_.TTY
bridg:StudyPersonnel.telecomAddress
urn:HSDBv1.0:[Principal_Investigator]_.URL
bridg:StudyPersonnel.telecomAddress
urn:HSDBv1.0:[Principal_Investigator]_.Phone
bridg:StudyPersonnel.telecomAddress
urn:HSDBv1.0:[Principal_Investigator]_.FAX
bridg:StudyPersonnel.telecomAddress
urn:HSDBv1.0:[Principal_Investigator]_.Email_Address
bridg:StudyPersonnel.telecomAddress
urn:WHO:Contact_for_Scientific_Queries_-_telephone
bridg:StudyPersonnel.telecomAddress
urn:WHO:Contact_for_Public_Queries_-_telephone
bridg:StudyPersonnel.telecomAddress
urn:WHO:Contact_for_Public_Queries_-_email
bridg:StudyPersonnel.telecomAddress
urn:WHO:Contact_for_Scientific_Queries_-_email
bridg:StudyPersonnel.telecomAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:StudyProtocolDocumentVersion.publicDescription
publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
false
bridg:StudyProtocolDocumentVersion.publicDescription
The textual summary of a document intended for the general population.
bridg:StudyProtocolDocumentVersion.publicDescription
urn:C3PR:Study.precisText
bridg:StudyProtocolDocumentVersion.publicDescription
urn:C3PRv2.9:StudyVersion.descriptionText
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTGOV:Brief_Summary
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTOM:Protocol.precisText
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTOM:Protocol.descriptionText
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRPv1.0:StudyProtocol.publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRPv1.0:InterventionalStudyProtocol.publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRPv1.0:ObservationalStudyProtocol.publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRPv3.8:StudyProtocol.publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRR:Study_synopsis
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRRr3:StudyProtocolDocument.publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRRr3:Study.briefSummary
bridg:StudyProtocolDocumentVersion.publicDescription
urn:CTRv1.0:StudyProtocolDocumentVersion.publicDescription
bridg:StudyProtocolDocumentVersion.publicDescription
urn:FDA_HL7_SD_SD_DSTU2012:StudyProtocol.text
bridg:StudyProtocolDocumentVersion.publicDescription
urn:HSDBv1.0:[Study].Study_Public_Description
bridg:StudyProtocolDocumentVersion.publicDescription
urn:LabViewer2.2:Study.precisText
bridg:StudyProtocolDocumentVersion.publicDescription
urn:caAERSv2.2:Study.descriptionText
bridg:StudyProtocolDocumentVersion.publicTitle
publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
false
bridg:StudyProtocolDocumentVersion.publicTitle
The title of the document intended for the general population.
bridg:StudyProtocolDocumentVersion.publicTitle
urn:AE:Study.name
bridg:StudyProtocolDocumentVersion.publicTitle
urn:C3PR:Study.shortTitleText
bridg:StudyProtocolDocumentVersion.publicTitle
urn:C3PRv2.9:StudyVersion.shortTitleText
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTGOV:Brief_Title
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTOM:Protocol.shortTitleText
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTR_Rr2:Title_of_the_trial_for_lay_people
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRPv1.0:StudyProtocol.publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRPv1.0:ObservationalStudyProtocol.publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRPv1.0:InterventionalStudyProtocol.publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRPv3.8:StudyProtocol.publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRR:Protocol_Short_Title
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRRr3:StudyProtocolDocument.publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:CTRv1.0:StudyProtocolDocumentVersion.publicTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:HSDBv1.0:[Study].Study_Short_Title
bridg:StudyProtocolDocumentVersion.publicTitle
urn:LabViewer2.2:Study.shortTitle
bridg:StudyProtocolDocumentVersion.publicTitle
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_TITLE
bridg:StudyProtocolDocumentVersion.publicTitle
urn:WHO:Public_Title
bridg:StudyProtocolDocumentVersion.publicTitle
urn:caAERSv2.2:Study.shortTitleText
bridg:StudyProtocolDocumentVersion.scientificDescription
scientificDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
false
bridg:StudyProtocolDocumentVersion.scientificDescription
The textual summary of a document that includes extended scientific or technical information.
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:C3PR:Study.descriptionText
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:C3PRv2.9:StudyVersion.precisText
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTGOV:Detailed_Description
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTRPv1.0:InterventionalStudyProtocol.scientificDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTRPv1.0:ObservationalStudyProtocol.scientificDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTRPv1.0:StudyProtocol.scientificDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTRPv3.8:StudyProtocol.scientificDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTRRr3:Study.detailedDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:CTRv1.0:StudyProtocolDocumentVersion.scientificDescription
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:HSDBv1.0:[Study].Study_Scientific_Description
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:PSCv2.6:Study.longTitle
bridg:StudyProtocolDocumentVersion.scientificDescription
urn:caAERSv2.2:Study.precisText
bridg:StudyProtocolVersion.accrualReportingMethodCode
accrualReportingMethodCode
bridg:StudyProtocolVersion.accrualReportingMethodCode
false
bridg:StudyProtocolVersion.accrualReportingMethodCode
A coded value specifying the technique that is used for reporting study subject accrual data to the study sponsor.
bridg:StudyProtocolVersion.accrualReportingMethodCode
complete
bridg:StudyProtocolVersion.accrualReportingMethodCode
abbreviated
bridg:StudyProtocolVersion.accrualReportingMethodCode
urn:CTRPv1.0:InterventionalStudyProtocol.accrualReportingMethodCode
bridg:StudyProtocolVersion.accrualReportingMethodCode
urn:CTRPv1.0:StudyProtocol.accrualReportingMethodCode
bridg:StudyProtocolVersion.accrualReportingMethodCode
urn:CTRPv1.0:ObservationalStudyProtocol.accrualReportingMethodCode
bridg:StudyProtocolVersion.accrualReportingMethodCode
urn:CTRPv3.8:StudyProtocol.accrualReportingMethodCode
bridg:StudyProtocolVersion.accrualReportingMethodCode
urn:CTRv1.0:StudyProtocolVersion.accrualReportingMethodCode
bridg:StudyProtocolVersion.accrualReportingMethodCode
urn:Statistics_v1.0:StudyProtocolVersion.accrualReportingMethodCode
bridg:StudyProtocolVersion.acronym
acronym
bridg:StudyProtocolVersion.acronym
false
bridg:StudyProtocolVersion.acronym
The non-unique initials or abbreviated name used for identification of the study.
bridg:StudyProtocolVersion.acronym
WHI for Women's Health Initiative
bridg:StudyProtocolVersion.acronym
urn:CTGOV:Acronym
bridg:StudyProtocolVersion.acronym
urn:CTR_Rr2:Abbreviated_title_of_trial
bridg:StudyProtocolVersion.acronym
urn:CTRPv1.0:StudyProtocol.acronym
bridg:StudyProtocolVersion.acronym
urn:CTRPv1.0:InterventionalStudyProtocol.acronym
bridg:StudyProtocolVersion.acronym
urn:CTRPv1.0:ObservationalStudyProtocol.acronym
bridg:StudyProtocolVersion.acronym
urn:CTRPv3.8:StudyProtocol.acronym
bridg:StudyProtocolVersion.acronym
urn:CTRR:Acronym
bridg:StudyProtocolVersion.acronym
urn:CTRRr3:Study.acronym
bridg:StudyProtocolVersion.acronym
urn:CTRv1.0:StudyProtocolVersion.acronym
bridg:StudyProtocolVersion.acronym
urn:HSDBv1.0:[Study].Study_Acronym
bridg:StudyProtocolVersion.acronym
urn:Statistics_v1.0:StudyProtocolVersion.acronym
bridg:StudyProtocolVersion.acronym
urn:WHO:Acronym
bridg:StudyProtocolVersion.adaptiveDesignIndicator
adaptiveDesignIndicator
bridg:StudyProtocolVersion.adaptiveDesignIndicator
false
bridg:StudyProtocolVersion.adaptiveDesignIndicator
Specifies whether the design of the study is expected to evolve during the execution of the study.
bridg:StudyProtocolVersion.adaptiveDesignIndicator
Adaptive Study Indicator
bridg:StudyProtocolVersion.adaptiveDesignIndicator
urn:CTRv1.0:StudyProtocolVersion.adaptiveDesignIndicator
bridg:StudyProtocolVersion.aeCodingSystem
aeCodingSystem
bridg:StudyProtocolVersion.aeCodingSystem
false
bridg:StudyProtocolVersion.aeCodingSystem
The coding system used for recording adverse events for a study.
bridg:StudyProtocolVersion.aeCodingSystem
urn:CTRPv1.0:InterventionalStudyProtocol.AECodingSystem
bridg:StudyProtocolVersion.aeCodingSystem
urn:CTRPv1.0:ObservationalStudyProtocol.AECodingSystem
bridg:StudyProtocolVersion.aeCodingSystem
urn:CTRPv1.0:StudyProtocol.AEcodingSystem
bridg:StudyProtocolVersion.aeCodingSystem
urn:CTRv1.0:StudyProtocolVersion.aeCodingSystem
bridg:StudyProtocolVersion.aeCodingSystem
urn:Statistics_v1.0:StudyProtocolVersion.aeCodingSystem
bridg:StudyProtocolVersion.aeCodingSystem
urn:caAERSv2.2:AETerminology
bridg:StudyProtocolVersion.amendmentGracePeriod
amendmentGracePeriod
bridg:StudyProtocolVersion.amendmentGracePeriod
false
bridg:StudyProtocolVersion.amendmentGracePeriod
The period of time during which sites can continue to accrue on an existing study version before they are required to switch to the new study version.
bridg:StudyProtocolVersion.amendmentGracePeriod
90 days
bridg:StudyProtocolVersion.amendmentGracePeriod
urn:C3PRv2.9:StudyVersion.gracePeriod
bridg:StudyProtocolVersion.amendmentGracePeriod
urn:CTRv1.0:StudyProtocolVersion.amendmentGracePeriod
bridg:StudyProtocolVersion.amendmentGracePeriod
urn:Statistics_v1.0:StudyProtocolVersion.amendmentGracePeriod
bridg:StudyProtocolVersion.companionCode
companionCode
bridg:StudyProtocolVersion.companionCode
false
bridg:StudyProtocolVersion.companionCode
A coded value specifying the type of ancillary study.
bridg:StudyProtocolVersion.companionCode
Embedded
bridg:StudyProtocolVersion.companionCode
Non-Stand-Alone Companion: This study is part of a master study and cannot be executed separately from it nor in association with another master study. The documentation for this kind of companion study is embedded in the protocol of the master study.
bridg:StudyProtocolVersion.companionCode
Non-Embedded
bridg:StudyProtocolVersion.companionCode
Non-Stand-Alone Companion: This study is documented separately from a master study
bridg:StudyProtocolVersion.companionCode
but must be performed as part of a master study or as part of several master studies.
bridg:StudyProtocolVersion.companionCode
Non-Embedded
bridg:StudyProtocolVersion.companionCode
Stand-Alone Companion: This study is a separately documented study that can be performed on its own or as a companion to one or more master studies.
bridg:StudyProtocolVersion.companionCode
Non-Companion/Independent: This study is documented and executed on its own and does not support co-execution with a master study. This kind of study may be a master study with companion studies of its own.
bridg:StudyProtocolVersion.companionCode
Changes to example codes will require revisiting the RIM-based BRIDG Model.
bridg:StudyProtocolVersion.companionCode
urn:C3PRv2.9:Study.standaloneIndicator
bridg:StudyProtocolVersion.companionCode
urn:C3PRv2.9:Study.companionIndicator
bridg:StudyProtocolVersion.companionCode
urn:CTRv1.0:StudyProtocolVersion.companionCode
bridg:StudyProtocolVersion.companionCode
urn:Statistics_v1.0:StudyProtocolVersion.companionCode
bridg:StudyProtocolVersion.conditionCodingSystem
conditionCodingSystem
bridg:StudyProtocolVersion.conditionCodingSystem
false
bridg:StudyProtocolVersion.conditionCodingSystem
The coding system used for recording conditions that are the focus of a study.
bridg:StudyProtocolVersion.conditionCodingSystem
urn:CTRv1.0:StudyProtocolVersion.conditionCodingSystem
bridg:StudyProtocolVersion.conditionCodingSystem
urn:Statistics_v1.0:StudyProtocolVersion.conditionCodingSystem
bridg:StudyProtocolVersion.conditionCodingSystem
urn:caAERSv2.2:DiseaseTerminology.diseaseCodeTerm
bridg:StudyProtocolVersion.delayedRegistryPostingIndicator
delayedRegistryPostingIndicator
bridg:StudyProtocolVersion.delayedRegistryPostingIndicator
false
bridg:StudyProtocolVersion.delayedRegistryPostingIndicator
Specifies whether there is to be a delay in the public disclosure of the study, as permitted by relevant local legislation or regulation.
bridg:StudyProtocolVersion.delayedRegistryPostingIndicator
The study includes a device NOT previously approved or cleared by the US FDA for any use, as specified in US Public Law 110-85, Title VIII, Section 801. Select Yes/No. If "Yes" is selected, full posting of the trial information on ClinicalTrials.gov will be delayed until after the device has been approved or cleared. At that time, it is the registrant's responsibility to change this selection to "No" and release the record for full publication.
bridg:StudyProtocolVersion.delayedRegistryPostingIndicator
urn:CTRPv3.8:StudyProtocol.delayedpostingIndicator
bridg:StudyProtocolVersion.delayedRegistryPostingIndicator
urn:CTRRr3:Study.delayedProtocolPostingIndicator
bridg:StudyProtocolVersion.designConfigurationCode
designConfigurationCode
bridg:StudyProtocolVersion.designConfigurationCode
false
bridg:StudyProtocolVersion.designConfigurationCode
A coded value specifying how subject or experimental unit exposures to treatment strategies (which may include controls such as no treatment) will be identified, for retrospective studies, or planned, for prospective studies, in order to characterize treatment effects and compare effects of different treatment strategies in a clinical or pre-clinical study. The configuration will specify whether a subject or experimental unit received or is to receive only one exposure or multiple exposures, and, if multiple exposures, whether those exposures were/are to be simultaneous or in series.
bridg:StudyProtocolVersion.designConfigurationCode
Parallel Group Design
bridg:StudyProtocolVersion.designConfigurationCode
Crossover Design
bridg:StudyProtocolVersion.designConfigurationCode
Factorial Designs
bridg:StudyProtocolVersion.designConfigurationCode
Cohort
bridg:StudyProtocolVersion.designConfigurationCode
Case-control
bridg:StudyProtocolVersion.designConfigurationCode
Case-only
bridg:StudyProtocolVersion.designConfigurationCode
Case-crossover
bridg:StudyProtocolVersion.designConfigurationCode
Ecologic or Community Studies
bridg:StudyProtocolVersion.designConfigurationCode
Family-based
bridg:StudyProtocolVersion.designConfigurationCode
The configuration usually requires randomization to one or more treatment arms, each arm being allocated a different (or no) treatment.
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTGOV:Intervention_Model
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTGOV:Study_Design
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTGOV:Observational_Study_Model
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRPv1.0:ObservationalStudyProtocol.studyModelCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRPv1.0:InterventionalStudyProtocol.designConfigurationCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRPv3.8:InterventionalStudyProtocol.designConfigurationCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRR:Description_of_study_design
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRR:Configuration
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRRr3:ObservationalStudy.studyModelCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRRr3:Study.designConfigurationCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:CTRv1.0:StudyProtocolVersion.designConfigurationCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:Statistics_v1.0:StudyProtocolVersion.designConfigurationCode
bridg:StudyProtocolVersion.designConfigurationCode
urn:WHO:Study_Type_Study_Design_Assignment
bridg:StudyProtocolVersion.mandatoryIndicator
mandatoryIndicator
bridg:StudyProtocolVersion.mandatoryIndicator
false
bridg:StudyProtocolVersion.mandatoryIndicator
Specifies whether the modifications contained in the study protocol version must be applied to all sites and subjects or study subjects that want to continue participating in the study.
bridg:StudyProtocolVersion.mandatoryIndicator
urn:CTRv1.0:StudyProtocolVersion.mandatoryIndicator
bridg:StudyProtocolVersion.mandatoryIndicator
urn:PSCv2.6:Amendment.mandatory
bridg:StudyProtocolVersion.mandatoryIndicator
urn:Statistics_v1.0:StudyProtocolVersion.mandatoryIndicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
multiInstitutionIndicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
false
bridg:StudyProtocolVersion.multiInstitutionIndicator
Specifies whether a study is designed to be conducted at more than one site concurrently.
bridg:StudyProtocolVersion.multiInstitutionIndicator
This could be conceived as derivable, but since it needs to be defined before study sites are associated with a study, it is needed here.
Derived when StudyProtocolVersion.participatingOrganizationTypeCode = "Multi Center".
Traditionally, the domain concept for this attribute is called "Multi-Institution" indicator, but the intent is to identify whether there will be multiple sites which will have separate IRB approvals, personnel training, regulatory affairs, consistent use of procedures, etc. So if a given institution has multiple sites associated with it and does IRB approval at the institution level, but has more than one site involved in the study, even if all the sites are part of the same institution, it is still multiInstitutionIndicator = "true".
bridg:StudyProtocolVersion.multiInstitutionIndicator
urn:C3PR:Study.multiInstitutionIndicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
urn:CTOM:Protocol.multiInstitutionIndicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
urn:CTRR:Multi_Institution_Indicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
urn:CTRv1.0:StudyProtocolVersion.multiInstitutionIndicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
urn:Statistics_v1.0:StudyProtocolVersion.multiInstitutionIndicator
bridg:StudyProtocolVersion.multiInstitutionIndicator
urn:caAERSv2.2:Study.multiInstitutionIndicator
bridg:StudyProtocolVersion.participatingLocationCode
participatingLocationCode
bridg:StudyProtocolVersion.participatingLocationCode
false
bridg:StudyProtocolVersion.participatingLocationCode
A coded value specifying the locations from which participants will be, are intended to be, or have been recruited for the study.
bridg:StudyProtocolVersion.participatingLocationCode
participating countries
bridg:StudyProtocolVersion.participatingLocationCode
participating states
bridg:StudyProtocolVersion.participatingLocationCode
urn:CTRR:Countries_of_Recruitment
bridg:StudyProtocolVersion.participatingLocationCode
urn:CTRRr3:Study.participatingCountryCode
bridg:StudyProtocolVersion.participatingLocationCode
urn:CTRv1.0:StudyProtocolVersion.participatingCountryCode
bridg:StudyProtocolVersion.participatingLocationCode
urn:HSDBv1.0:[Study].location_of_study
bridg:StudyProtocolVersion.participatingLocationCode
urn:Statistics_v1.0:StudyProtocolVersion.participatingCountryCode
bridg:StudyProtocolVersion.participatingLocationCode
urn:WHO:Countries_of_Recruitment
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
participatingOrganizationTypeCode
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
false
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
A coded value specifying the kind of organizations planned to participate as study sites for this study.
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Cancer Center
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Clinical Center
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Consortium
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Group
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Intergroup
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Multi-Center
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Network
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
Single Institution
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
urn:CTRPv1.0:InterventionalStudyProtocol.participatingOrganizationTypeCode
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
urn:CTRPv1.0:ObservationalStudyProtocol.participatingOrganizationTypeCode
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
urn:CTRPv1.0:StudyProtocol.participatingOrganizationTypeCode
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
urn:CTRv1.0:StudyProtocolVersion.participatingOrganizationTypeCode
bridg:StudyProtocolVersion.participatingOrganizationTypeCode
urn:Statistics_v1.0:StudyProtocolVersion.participatingOrganizationTypeCode
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
periodicTargetAccrualNumber
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
false
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
A ratio representing the number of study subjects to be accrued per a specified amount of time.
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
For monthly target accrual
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
a given study may have a target accrual of 100 per 1 month meaning the numerator of the ratio is the integer 100 and the denominator is a PQ where the value is 1 and the unit is month.
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
urn:CTRPv1.0:InterventionalStudyProtocol.monthlyTargetAccrualNumber
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
urn:CTRPv1.0:ObservationalStudyProtocol.monthlyTargetAccrualNumber
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
urn:CTRPv1.0:StudyProtocol.monthlyTargetAccrualNumber
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
urn:CTRPv3.8:StudyProtocol.monthlyTargetAccrualNumber
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
urn:CTRv1.0:StudyProtocolVersion.periodicTargetAccrualNumber
bridg:StudyProtocolVersion.periodicTargetAccrualNumber
urn:Statistics_v1.0:StudyProtocolVersion.periodicTargetAccrualNumber
bridg:StudyProtocolVersion.phaseCode
phaseCode
bridg:StudyProtocolVersion.phaseCode
false
bridg:StudyProtocolVersion.phaseCode
A coded value specifying a stage in the progression of a therapy from initial experimental use in humans in clinical trials to post-market evaluation.
bridg:StudyProtocolVersion.phaseCode
I
bridg:StudyProtocolVersion.phaseCode
I/II
bridg:StudyProtocolVersion.phaseCode
II
bridg:StudyProtocolVersion.phaseCode
III
bridg:StudyProtocolVersion.phaseCode
N/A
bridg:StudyProtocolVersion.phaseCode
Studies are generally categorized into four (sometimes five) phases described separately herein. An investigational medicine or product may be evaluated in two or more phases simultaneously in different studies, and some studies may overlap two different phases. Phase 1: The initial introduction of an investigational new drug into humans. Phase 1 studies are typically closely monitored and may be conducted in patients or normal volunteer subjects. Phase 2: Controlled clinical studies conducted to evaluate the effectiveness of the drug for a particular indication or indications in patients with the disease or condition under study and to determine the common short-term side effects and risks associated with the drug. Phase 3: Studies are expanded controlled and uncontrolled. They are performed after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather the additional information about effectiveness and safety that is needed to evaluate the overall benefit-risk relationship of the drug and to provide an adequate basis for physician labeling. Phase 3b: Phase 3b studies are a sub category of phase 3 near the time of approval to elicit additional findings. Phase 4: Concurrent with marketing approval, Food and Drug Administration (FDA) may seek agreement from the sponsor to conduct certain post-marketing (phase 4) studies to delineate additional information about the drug's risks, benefits, and optimal use. Phase 5: Post-marketing surveillance is sometimes referred to as Phase 5.
bridg:StudyProtocolVersion.phaseCode
urn:C3PR:Study.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:C3PRv2.9:Study.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:CTGOV:Study_Design_Study_Phase
bridg:StudyProtocolVersion.phaseCode
urn:CTOM:Protocol.phaseCode
Phase III
bridg:StudyProtocolVersion.phaseCode
urn:CTR_Rr2:Trial_type_Therapeutic_Confirmatory
Phase I
bridg:StudyProtocolVersion.phaseCode
urn:CTR_Rr2:Trial_type_Human_pharmacology
Phase II
bridg:StudyProtocolVersion.phaseCode
urn:CTR_Rr2:Trial_type_Therapeutic_Exploratory
Phase IV
bridg:StudyProtocolVersion.phaseCode
urn:CTR_Rr2:Trial_type_Therapeutic_Use
bridg:StudyProtocolVersion.phaseCode
urn:CTRPv1.0:ObservationalStudyProtocol.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:CTRPv1.0:InterventionalStudyProtocol.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:CTRPv1.0:StudyProtocol.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:CTRPv3.8:StudyProtocol.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:CTRR:Clinical_Trial_Phase
bridg:StudyProtocolVersion.phaseCode
urn:CTRRr3:Study.typeCode
bridg:StudyProtocolVersion.phaseCode
urn:CTRRr3:Study.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:CTRv1.0:StudyProtocolVersion.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:HSDBv1.0:[Study].Phase
bridg:StudyProtocolVersion.phaseCode
urn:LabViewer2.2:Study.phase
bridg:StudyProtocolVersion.phaseCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_TPHASE
bridg:StudyProtocolVersion.phaseCode
urn:Statistics_v1.0:StudyProtocolVersion.phaseCode
bridg:StudyProtocolVersion.phaseCode
urn:WHO:Study_Type.Phase
bridg:StudyProtocolVersion.phaseCode
urn:caAERSv2.2:Study.phaseCode
bridg:StudyProtocolVersion.plannedDuration
plannedDuration
bridg:StudyProtocolVersion.plannedDuration
false
bridg:StudyProtocolVersion.plannedDuration
The intended period of time for the study.
bridg:StudyProtocolVersion.plannedDuration
urn:CTR_Rr2:PlannedActivity.plannedDuration
bridg:StudyProtocolVersion.plannedDuration
urn:CTRv1.0:StudyProtocolVersion.plannedDuration
bridg:StudyProtocolVersion.plannedDuration
urn:HSDBv1.0:[Study].Study_duration
bridg:StudyProtocolVersion.plannedDuration
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_LENGTH
bridg:StudyProtocolVersion.plannedDuration
urn:Statistics_v1.0:StudyProtocolVersion.plannedDuration
bridg:StudyProtocolVersion.plannedSiteNumberRange
plannedSiteNumberRange
bridg:StudyProtocolVersion.plannedSiteNumberRange
false
bridg:StudyProtocolVersion.plannedSiteNumberRange
An integer falling within minimum and maximum bounds that specifies how many study sites are expected to participate in the conduction of the study.
bridg:StudyProtocolVersion.plannedSiteNumberRange
Relevant before specific sites have been selected. Can be derived once sites have been selected.
bridg:StudyProtocolVersion.plannedSiteNumberRange
urn:CTRv1.0:StudyProtocolVersion.plannedSiteNumber
bridg:StudyProtocolVersion.plannedStudySubjectExperience
plannedStudySubjectExperience
bridg:StudyProtocolVersion.plannedStudySubjectExperience
false
bridg:StudyProtocolVersion.plannedStudySubjectExperience
A description of what the study subject can expect to experience over the course of the study, including the sequence and duration of activities.
bridg:StudyProtocolVersion.plannedStudySubjectExperience
The description
bridg:StudyProtocolVersion.plannedStudySubjectExperience
sequence and duration of study epochs
bridg:StudyProtocolVersion.plannedStudySubjectExperience
including pre-randomization and post-treatment epochs
bridg:StudyProtocolVersion.plannedStudySubjectExperience
therapy withdrawal epochs
bridg:StudyProtocolVersion.plannedStudySubjectExperience
and single- and double-blind treatment epochs.
bridg:StudyProtocolVersion.plannedStudySubjectExperience
urn:CTRR:Planned_Subject_Participation_Experience
bridg:StudyProtocolVersion.plannedStudySubjectExperience
urn:CTRRr3:Study.plannedStudySubjectExperience
bridg:StudyProtocolVersion.plannedStudySubjectExperience
urn:CTRv1.0:StudyProtocolVersion.plannedStudySubjectExperience
ICH
bridg:StudyProtocolVersion.plannedStudySubjectExperience
urn:PRM:Planned_Subject_Participation_Experience
bridg:StudyProtocolVersion.plannedStudySubjectExperience
urn:Statistics_v1.0:StudyProtocolVersion.plannedStudySubjectExperience
bridg:StudyProtocolVersion.populationDescription
populationDescription
bridg:StudyProtocolVersion.populationDescription
false
bridg:StudyProtocolVersion.populationDescription
The textual representation of the subject characteristics, including inclusion and exclusion criteria and describes the population for which the study may be generalized.
bridg:StudyProtocolVersion.populationDescription
This would include all subgroups as well.
bridg:StudyProtocolVersion.populationDescription
urn:CTGOV:Study_Population_Description
bridg:StudyProtocolVersion.populationDescription
urn:CTR_Rr2:Population_healthy_volunteers
bridg:StudyProtocolVersion.populationDescription
urn:CTRPv1.0:ObservationalStudyProtocol.studyPopulationDescription
bridg:StudyProtocolVersion.populationDescription
urn:CTRPv1.0:ObservationalStudyProtocol.populationDescription
bridg:StudyProtocolVersion.populationDescription
urn:CTRPv1.0:InterventionalStudyProtocol.populationDescription
bridg:StudyProtocolVersion.populationDescription
urn:CTRPv1.0:StudyProtocol.populationDescription
bridg:StudyProtocolVersion.populationDescription
urn:CTRR:Target_study_population_description
bridg:StudyProtocolVersion.populationDescription
urn:CTRRr3:Study.populationDescription
bridg:StudyProtocolVersion.populationDescription
urn:CTRv1.0:StudyProtocolVersion.populationDescription
bridg:StudyProtocolVersion.populationDescription
urn:Statistics_v1.0:StudyProtocolVersion.populationDescription
s or Problem(s Studied
bridg:StudyProtocolVersion.populationDescription
urn:WHO:Health_Condition
bridg:StudyProtocolVersion.primaryPurposeTypeCode
primaryPurposeTypeCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
false
bridg:StudyProtocolVersion.primaryPurposeTypeCode
A coded value specifying the type of study based upon the intent of the study's activities. A classification of the intent of the study.
bridg:StudyProtocolVersion.primaryPurposeTypeCode
Treatment studies test new treatments
bridg:StudyProtocolVersion.primaryPurposeTypeCode
new combinations of drugs
bridg:StudyProtocolVersion.primaryPurposeTypeCode
or new approaches to surgery or radiation therapy.
bridg:StudyProtocolVersion.primaryPurposeTypeCode
Prevention studies look for better ways to prevent disease in people who have never had the disease or to prevent a disease from returning. These approaches may include medicines
bridg:StudyProtocolVersion.primaryPurposeTypeCode
vitamins
bridg:StudyProtocolVersion.primaryPurposeTypeCode
vaccines
bridg:StudyProtocolVersion.primaryPurposeTypeCode
minerals
bridg:StudyProtocolVersion.primaryPurposeTypeCode
or lifestyle changes.
bridg:StudyProtocolVersion.primaryPurposeTypeCode
Diagnostic studies are conducted to find better tests or procedures for diagnosing a particular disease or condition.
bridg:StudyProtocolVersion.primaryPurposeTypeCode
Screening studies test the best way to detect certain diseases or health conditions.
bridg:StudyProtocolVersion.primaryPurposeTypeCode
Quality of Life studies (or Supportive Care studies) explore ways to improve comfort and the quality of life for individuals with a chronic illness.
bridg:StudyProtocolVersion.primaryPurposeTypeCode
StudyProtocolVersion.purposeStatement, StudyProtocolVersion.primaryPurposeTypeCode and StudyObjective may sound similar in meaning but are distinct concepts in BRIDG. StudyProtocolVersion.purposeStatement, which is an broad explanation of why a study is being conducted (e.g. determine efficacy of a drug or procedure), differs from StudyProtocolVersion.primaryPurposeTypeCode which is a classification of the purpose or intent of the study (e.g. Prevention, Treatment, Quality of Life), and that differs from StudyObjective, which describes in a specific and measurable way what the study hopes to accomplish (e.g. extend life of subjects at least 3 years, reduce frequency of symptoms).
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:C3PR:Study.type
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:C3PRv2.9:Study.type
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTGOV:Intervention_Type
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTGOV:Study_Design_Primary_Purpose
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTOM:Protocol.intentCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTR_Rr2:Trial_type_Bioequivalence_Study
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTR_Rr2:Trial_type_Other_specification
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTR_Rr2:Trial_type_First_administration_to_humans
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTR_Rr2:Trial_type_Other
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRPv1.0:InterventionalStudyProtocol.primaryPurposeCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRPv1.0:ObservationalStudyProtocol.primaryPurposeCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRPv1.0:StudyProtocol.primaryPurposeCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRPv3.8:StudyProtocol.primaryPurposeCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRPv3.8:StudyProtocol.primaryPurposeOtherText
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRR:Primary_Purpose
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRR:Intervention_Type
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRRr3:Study.primaryPurposeCode
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:CTRv1.0:StudyProtocolVersion.primaryPurposeCode
in IndividualCaseSafetyReport
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:ICSRr2:ResearchStudy.code
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_TINDTP
bridg:StudyProtocolVersion.primaryPurposeTypeCode
urn:Statistics_v1.0:StudyProtocolVersion.primaryPurposeCode
bridg:StudyProtocolVersion.purposeStatement
purposeStatement
bridg:StudyProtocolVersion.purposeStatement
false
bridg:StudyProtocolVersion.purposeStatement
A statement describing the overall intent of the study. This field describes the contribution of this study to product development, treatment strategies, prevention approaches, diagnostic techniques, or patient quality of life, i.e., what knowledge is being contributed from the conduct of this study.
bridg:StudyProtocolVersion.purposeStatement
test the efficacy of a particular cancer treatment
bridg:StudyProtocolVersion.purposeStatement
StudyProtocolVersion.purposeStatement, StudyProtocolVersion.primaryPurposeTypeCode and StudyObjective may sound similar in meaning but are distinct concepts in BRIDG. StudyProtocolVersion.purposeStatement, which is an broad explanation of why a study is being conducted (e.g. determine efficacy of a drug or procedure), differs from StudyProtocolVersion.primaryPurposeTypeCode which is a classification of the purpose or intent of the study (e.g. Prevention, Treatment, Quality of Life), and that differs from StudyObjective, which describes in a specific and measurable way what the study hopes to accomplish (e.g. extend life of subjects at least 3 years, reduce frequency of symptoms).
bridg:StudyProtocolVersion.purposeStatement
urn:CTRR:Trial_Purpose_Summary
bridg:StudyProtocolVersion.purposeStatement
urn:CTRRr3:Study.purposeStatement
bridg:StudyProtocolVersion.purposeStatement
urn:CTRv1.0:StudyProtocolVersion.purposeStatement
bridg:StudyProtocolVersion.purposeStatement
urn:PRM:Trial_Purpose_Summary
bridg:StudyProtocolVersion.purposeStatement
urn:Statistics_v1.0:StudyProtocolVersion.purposeStatement
bridg:StudyProtocolVersion.responsiblePartyCode
responsiblePartyCode
bridg:StudyProtocolVersion.responsiblePartyCode
false
bridg:StudyProtocolVersion.responsiblePartyCode
A coded value specifying the type of entity who is legally responsible for the execution of the study.
bridg:StudyProtocolVersion.responsiblePartyCode
PI
bridg:StudyProtocolVersion.responsiblePartyCode
sponsor
bridg:StudyProtocolVersion.responsiblePartyCode
urn:CTGOV:Responsible_Party
bridg:StudyProtocolVersion.responsiblePartyCode
urn:CTRPv1.0:InterventionalStudyProtocol.responsiblePartyCode
bridg:StudyProtocolVersion.responsiblePartyCode
urn:CTRPv1.0:ObservationalStudyProtocol.responsiblePartyCode
bridg:StudyProtocolVersion.responsiblePartyCode
urn:CTRPv1.0:StudyProtocol.responsiblePartyCode
bridg:StudyProtocolVersion.responsiblePartyCode
urn:CTRRr3:StudyColleague.responsiblePartyIndicator
bridg:StudyProtocolVersion.responsiblePartyCode
urn:CTRv1.0:StudyProtocolVersion.responsiblePartyCode
bridg:StudyProtocolVersion.responsiblePartyCode
urn:Statistics_v1.0:StudyProtocolVersion.responsiblePartyCode
bridg:StudyProtocolVersion.studySchematic
studySchematic
bridg:StudyProtocolVersion.studySchematic
false
bridg:StudyProtocolVersion.studySchematic
Diagram which outlines all study epochs, timing of randomization and duration of treatments.
bridg:StudyProtocolVersion.studySchematic
urn:CTRPv1.0:InterventionalStudyProtocol.studySchematic
bridg:StudyProtocolVersion.studySchematic
urn:CTRPv1.0:StudyProtocol.studySchematic
bridg:StudyProtocolVersion.studySchematic
urn:CTRPv1.0:ObservationalStudyProtocol.studySchematic
bridg:StudyProtocolVersion.studySchematic
urn:CTRR:Study_schematic/flow_chart
bridg:StudyProtocolVersion.studySchematic
urn:CTRRr3:Study.studySchematic
bridg:StudyProtocolVersion.studySchematic
urn:CTRv1.0:StudyProtocolVersion.studySchematic
bridg:StudyProtocolVersion.studySchematic
urn:Statistics_v1.0:StudyProtocolVersion.studySchematic
bridg:StudyProtocolVersion.studySubjectTypeCode
studySubjectTypeCode
bridg:StudyProtocolVersion.studySubjectTypeCode
false
bridg:StudyProtocolVersion.studySubjectTypeCode
A coded value specifying the kind of study subject involved in the study or investigation.
bridg:StudyProtocolVersion.studySubjectTypeCode
human
bridg:StudyProtocolVersion.studySubjectTypeCode
rat
bridg:StudyProtocolVersion.studySubjectTypeCode
mouse
bridg:StudyProtocolVersion.studySubjectTypeCode
x-ray machine
bridg:StudyProtocolVersion.studySubjectTypeCode
This attribute is explicitly not meant to represent parts of study subjects that may be studied, such as a human eye, or groups of study subjects such as a herd of cows. It is meant to represent the whole individual that is registered as a study subject.
bridg:StudyProtocolVersion.studySubjectTypeCode
urn:CTRv1.0:StudyProtocolVersion.studySubjectTypeCode
bridg:StudyProtocolVersion.studySubjectTypeCode
urn:HL7SP:StudyParticipation_RMIM
bridg:StudyProtocolVersion.studySubjectTypeCode
urn:Statistics_v1.0:StudyProtocolVersion.studySubjectTypeCode
bridg:StudyProtocolVersion.targetAccrualNumberRange
targetAccrualNumberRange
bridg:StudyProtocolVersion.targetAccrualNumberRange
false
bridg:StudyProtocolVersion.targetAccrualNumberRange
An integer falling within minimum and maximum bounds that specifies how many study subjects are to be accrued for the study.
bridg:StudyProtocolVersion.targetAccrualNumberRange
A typical target accrual number (always assumed to be a minimum target) would be targetAccrualNumberRange.IVL<INT>.low, a maximum target accrual would be targetAccrualNumberRange.IVL<INT>.high.
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:C3PR:Study.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:C3PRv2.9:Study.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTGOV:Enrollment
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTOM:Protocol.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTR_Rr2:Population_planned_numbers_in_whole_trial
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv1.0:StudyProtocol.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv1.0:ObservationalStudyProtocol.targetAnatomicSiteCode.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv1.0:StudyProtocol.maximumTargetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv1.0:InterventionalStudyProtocol.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv1.0:InterventionalStudyProtocol.maximumTargetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv1.0:ObservationalStudyProtocol.maximumTargetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv3.8:StudyProtocol.maximumTargetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRPv3.8:StudyProtocol.targetAccrualNumber
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRR:Targeted_Accrual
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRRr3:Study.targetAccrualNumberRange
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:CTRv1.0:StudyProtocolVersion.targetAccrualNumberRange
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:HSDBv1.0:[Study].Targeted_Accrual
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:SDTM_IGv3.1.2:TS.TSVAL_where_TSPARMCD_PLANSUB
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:Statistics_v1.0:StudyProtocolVersion.targetAccrualNumberRange
bridg:StudyProtocolVersion.targetAccrualNumberRange
urn:WHO:Target_Sample_Size
bridg:StudyProtocolVersion.targetAnatomicSiteCode
targetAnatomicSiteCode
bridg:StudyProtocolVersion.targetAnatomicSiteCode
false
bridg:StudyProtocolVersion.targetAnatomicSiteCode
A coded value specifying the anatomic location that is the focus of a study.
bridg:StudyProtocolVersion.targetAnatomicSiteCode
breast
bridg:StudyProtocolVersion.targetAnatomicSiteCode
ovary
bridg:StudyProtocolVersion.targetAnatomicSiteCode
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:StudyProtocolVersion.targetAnatomicSiteCode
urn:CTRPv1.0:InterventionalStudyProtocol.targetAnatomicSiteCode
bridg:StudyProtocolVersion.targetAnatomicSiteCode
urn:CTRPv1.0:ObservationalStudyProtocol.targetAnatomicSiteCode
bridg:StudyProtocolVersion.targetAnatomicSiteCode
urn:CTRPv1.0:StudyProtocol.targetAnatomicSiteCode
bridg:StudyProtocolVersion.targetAnatomicSiteCode
urn:CTRPv3.8:StudyProtocol.targetAnatomicSiteCode
bridg:StudyProtocolVersion.targetAnatomicSiteCode
urn:CTRv1.0:StudyProtocolVersion.targetAnatomicSiteCode
bridg:StudyProtocolVersion.targetAnatomicSiteCode
urn:Statistics_v1.0:StudyProtocolVersion.targetAnatomicSiteCode
bridg:StudyProtocolVersion.therapeuticAreaCode
therapeuticAreaCode
bridg:StudyProtocolVersion.therapeuticAreaCode
false
bridg:StudyProtocolVersion.therapeuticAreaCode
A coded value specifying the field of knowledge that focuses on research and development of treatments for diseases and pathologic findings, as well as prevention of conditions that negatively impact the health of an individual.
bridg:StudyProtocolVersion.therapeuticAreaCode
eye disease
bridg:StudyProtocolVersion.therapeuticAreaCode
nervous system disease
bridg:StudyProtocolVersion.therapeuticAreaCode
urn:CTRPv3.8:StudyProtocol.programCodeText
bridg:StudyProtocolVersion.therapeuticAreaCode
urn:CTRRr3:Study.therapeuticAreaCode
bridg:StudyRecruitmentStatus.code
code
bridg:StudyRecruitmentStatus.code
false
bridg:StudyRecruitmentStatus.code
A coded value specifying the phase in the lifecycle of recruitment for the study.
bridg:StudyRecruitmentStatus.code
Not yet recruiting; recruiting; enrolling by invitation; active
bridg:StudyRecruitmentStatus.code
not recruiting; completed; suspended; terminated; withdrawn.
bridg:StudyRecruitmentStatus.code
The recruitment status of a study may overlap with the study site status and accrual status. This overlap needs to be clearly differentiated. (See tracker issue 29398). A proposed solution is to eliminate the study recruitment status codes and adopt the CTRP values for study status code.
bridg:StudyRecruitmentStatus.code
urn:CTGOV:Overall_Recruitment_Status
bridg:StudyRecruitmentStatus.code
urn:CTGOV:Recruitment_Status
bridg:StudyRecruitmentStatus.code
urn:CTRPv1.0:StudyRecruitmentStatus.statusCode
bridg:StudyRecruitmentStatus.code
urn:CTRPv3.8:StudyRecruitmentStatus.statusCode
bridg:StudyRecruitmentStatus.code
urn:CTRR:Recruitment_Status
bridg:StudyRecruitmentStatus.code
urn:CTRRr3:StudyRecruitmentStatus.statusCode
bridg:StudyRecruitmentStatus.code
urn:CTRv1.0:StudyRecruitmentStatus.code
bridg:StudyRecruitmentStatus.code
urn:WHO:Recruitment_Status
bridg:StudyRecruitmentStatus.date
date
bridg:StudyRecruitmentStatus.date
false
bridg:StudyRecruitmentStatus.date
The date (and time) on which the recruitment status is assigned.
bridg:StudyRecruitmentStatus.date
urn:CTRPv1.0:StudyRecruitmentStatus.statusDate
bridg:StudyRecruitmentStatus.date
urn:CTRPv3.8:StudyRecruitmentStatus.statusDate
bridg:StudyRecruitmentStatus.date
urn:CTRv1.0:StudyRecruitmentStatus.date
bridg:StudyReference.citationDescription
citationDescription
bridg:StudyReference.citationDescription
false
bridg:StudyReference.citationDescription
A bibliographical reference in a format acceptable to the publisher of the reference material.
bridg:StudyReference.citationDescription
Studies performed in the United States may be required to conform to the National Library of Medicine's MEDLINE format.
bridg:StudyReference.citationDescription
urn:CTGOV:Citation
bridg:StudyReference.citationDescription
urn:CTRR:Published_Results_Citation
bridg:StudyReference.citationDescription
urn:CTRRr3:StudyReference.citationDescription
bridg:StudyReference.citationDescription
urn:CTRv1.0:StudyReference.citationDescription
bridg:StudyReference.linkPageDescription
linkPageDescription
bridg:StudyReference.linkPageDescription
false
bridg:StudyReference.linkPageDescription
The textual representation of the linked page.
bridg:StudyReference.linkPageDescription
If the page being linked is the protocol's home page on the sponsor's Web site
bridg:StudyReference.linkPageDescription
the description might be "This is a link to the study sponsor's web site".
bridg:StudyReference.linkPageDescription
urn:CTGOV:Links_Description
bridg:StudyReference.linkPageDescription
urn:CTRRr3:StudyReference.linkPageDescription
bridg:StudyReference.linkPageDescription
urn:CTRv1.0:StudyReference.linkPageDescription
bridg:StudyReference.publicationIdentifier
publicationIdentifier
bridg:StudyReference.publicationIdentifier
false
bridg:StudyReference.publicationIdentifier
A unique symbol that establishes identity of a publication related to the study protocol background.
bridg:StudyReference.publicationIdentifier
10987815 is the unique PubMed Identifier (PMID) for the citation in MEDLINE.
bridg:StudyReference.publicationIdentifier
urn:CTGOV:MEDLINE_Identifier
bridg:StudyReference.publicationIdentifier
urn:CTRR:Published_Results_Identifier
bridg:StudyReference.publicationIdentifier
urn:CTRRr3:StudyReference.publicationIdentifier
bridg:StudyReference.publicationIdentifier
urn:CTRv1.0:StudyReference.publicationIdentifier
bridg:StudyReference.publicationName
publicationName
bridg:StudyReference.publicationName
false
bridg:StudyReference.publicationName
A non-unique textual identifier specifying the human-readable name of the publication.
bridg:StudyReference.publicationName
MEDLINE is the source for PMID 10987815
bridg:StudyReference.publicationName
urn:CTRR:Published_Results_Title
bridg:StudyReference.publicationName
urn:CTRRr3:StudyReference.publicationName
bridg:StudyReference.publicationName
urn:CTRv1.0:StudyReference.publicationName
bridg:StudyReference.publicationName
urn:PRM:PublishedResults.title
bridg:StudyReference.uniformResourceLocator
uniformResourceLocator
bridg:StudyReference.uniformResourceLocator
false
bridg:StudyReference.uniformResourceLocator
A complete reference to a website (including http://) that is directly relevant to the study.
bridg:StudyReference.uniformResourceLocator
http://www.alzheimers.org/
bridg:StudyReference.uniformResourceLocator
urn:CTGOV:Links_URL
bridg:StudyReference.uniformResourceLocator
urn:CTRRr3:StudyReference.universalResourceLocator
bridg:StudyReference.uniformResourceLocator
urn:CTRv1.0:StudyReference.uniformResourceLocator
bridg:StudyRegistry.acronym
acronym
bridg:StudyRegistry.acronym
false
bridg:StudyRegistry.acronym
The non-unique initials or abbreviated name used for identification of the registry.
bridg:StudyRegistry.acronym
NTR (Netherlands National Trial Register)
bridg:StudyRegistry.acronym
urn:CTRR:Registry
bridg:StudyRegistry.acronym
urn:CTRRr3:StudyRegistry.acronym
bridg:StudyRegistry.acronym
urn:CTRv1.0:StudyRegistry.acronym
bridg:StudyRegistry.acronym
urn:WHO:Primary_Registry
bridg:StudyRegistry.name
name
bridg:StudyRegistry.name
false
bridg:StudyRegistry.name
A non-unique textual identifier for the registry.
bridg:StudyRegistry.name
ClinicalTrials.gov
bridg:StudyRegistry.name
urn:CTRR:Registry
bridg:StudyRegistry.name
urn:CTRRr3:StudyRegistry.name
bridg:StudyRegistry.name
urn:CTRv1.0:StudyRegistry.name
bridg:StudyRegistry.name
urn:WHO:Primary_Registry
bridg:StudyResource.effectiveDateRange
effectiveDateRange
bridg:StudyResource.effectiveDateRange
false
bridg:StudyResource.effectiveDateRange
The date and time span for when the study resource is active.
bridg:StudyResource.effectiveDateRange
urn:CTRPv1.0:StudyResourcing.activeIndicator
bridg:StudyResource.effectiveDateRange
urn:CTRPv3.8:StudyResourcing.activeIndicator
bridg:StudyResource.effectiveDateRange
urn:CTRv1.0:StudyResource.effectiveDateRange
bridg:StudyResource.effectiveDateRange
urn:HL7SP:Service_Provider.effectiveTime
bridg:StudyResource.inactiveComment
inactiveComment
bridg:StudyResource.inactiveComment
false
bridg:StudyResource.inactiveComment
Additional description why the resource is no longer active.
bridg:StudyResource.inactiveComment
urn:CTRPv1.0:StudyResourcing.inactiveCommentText
bridg:StudyResource.inactiveComment
urn:CTRPv3.8:StudyResourcing.inactiveCommentText
bridg:StudyResource.primaryIndicator
primaryIndicator
bridg:StudyResource.primaryIndicator
false
bridg:StudyResource.primaryIndicator
Specifies whether this is the main or principal study resource.
bridg:StudyResource.primaryIndicator
This distinguishes between an organization that is the primary funder vs. a funder who provides less money for a study.
bridg:StudyResource.primaryIndicator
urn:CTRPv1.0:StudyResourceProvider.primaryIndicator
bridg:StudyResource.primaryIndicator
urn:CTRv1.0:StudyResource.primaryIndicator
bridg:StudySite.accrualStatusCode
accrualStatusCode
bridg:StudySite.accrualStatusCode
false
bridg:StudySite.accrualStatusCode
A coded value specifying the phase in the lifecycle of a participating site relative to the enrollment of additional experimental units in the given study.
bridg:StudySite.accrualStatusCode
Open to accrual
bridg:StudySite.accrualStatusCode
Closed to accrual
bridg:StudySite.accrualStatusCode
Temporarily closed to accrual
bridg:StudySite.accrualStatusCode
Pending accrual
bridg:StudySite.accrualStatusCode
Please refer to the Study Site Accrual Status state transition diagram for further details.
The accrual status of a study site may overlap with the overall status of the study and study site status. This overlap needs to be clearly differentiated. (See tracker issue 29398). A proposed solution is to eliminate the study site accrual status codes and adopt the CTRP values for study site status code.
bridg:StudySite.accrualStatusCode
urn:CTRv1.0:StudySite.accrualStatusCode
bridg:StudySite.accrualStatusDate
accrualStatusDate
bridg:StudySite.accrualStatusDate
false
bridg:StudySite.accrualStatusDate
The date (and time) on which the accrual status is established.
bridg:StudySite.accrualStatusDate
urn:CTRv1.0:StudySite.accrualStatusDate
bridg:StudySite.dateRange
dateRange
bridg:StudySite.dateRange
false
bridg:StudySite.dateRange
The date and time span specifying when the site's participation in the study begins and ends.
bridg:StudySite.dateRange
urn:C3PR:StudySite.endDate
bridg:StudySite.dateRange
urn:C3PR:StudySite.startDate
bridg:StudySite.dateRange
urn:CTGOV:StudySite.startDate
bridg:StudySite.dateRange
urn:CTOM:StudySite.stopDate
bridg:StudySite.dateRange
urn:CTRPv1.0:StudyParticipation.dateRange
bridg:StudySite.dateRange
urn:CTRv1.0:StudySite.dateRange
bridg:StudySite.identifier
identifier
bridg:StudySite.identifier
false
bridg:StudySite.identifier
A unique symbol that establishes identity of the study site.
bridg:StudySite.identifier
urn:CDASHv1.1:DM.SITEID
bridg:StudySite.identifier
urn:CTRPv3.8:StudySite.localStudyProtocolIdentifier
bridg:StudySite.identifier
urn:CTRv1.0:StudySite.identifier
bridg:StudySite.identifier
urn:HL7SP:StudySite.id
bridg:StudySite.identifier
urn:SDTM_IGv3.1.1:DM.SITEID
bridg:StudySite.identifier
urn:SDTM_IGv3.1.2:DM.SITEID
bridg:StudySite.leadIndicator
leadIndicator
bridg:StudySite.leadIndicator
false
bridg:StudySite.leadIndicator
Specifies whether this is the principal administrative organization responsible for the study.
bridg:StudySite.leadIndicator
Exception: A multi-site study with no single assigned coordination center; in this case, every participating organization can be named as lead organization.
bridg:StudySite.leadIndicator
urn:C3PR:StudySite.roleCode
bridg:StudySite.leadIndicator
urn:CTOM:StudySite.roleCode
bridg:StudySite.leadIndicator
urn:CTRv1.0:StudySite.leadIndicator
bridg:StudySite.plannedDuration
plannedDuration
bridg:StudySite.plannedDuration
false
bridg:StudySite.plannedDuration
The intended period of time for the study site's participation in the study.
bridg:StudySite.plannedDuration
urn:CTR_Rr2:Estimated_trial_duration_worldwide_months
bridg:StudySite.plannedDuration
urn:CTR_Rr2:Estimated_trial_duration_worldwide_years
bridg:StudySite.plannedDuration
urn:CTR_Rr2:Estimated_trial_duration_in_MS_days
bridg:StudySite.plannedDuration
urn:CTR_Rr2:Estimated_trial_duration_in_MS_years
bridg:StudySite.plannedDuration
urn:CTR_Rr2:Estimated_trial_duration_worldwide_days
bridg:StudySite.plannedDuration
urn:CTR_Rr2:Estimated_trial_duration_in_MS_months
bridg:StudySite.plannedDuration
urn:CTRRr3:Study.duration
bridg:StudySite.plannedDuration
urn:CTRv1.0:StudySite.plannedDuration
bridg:StudySite.statusCode
statusCode
bridg:StudySite.statusCode
false
bridg:StudySite.statusCode
A coded value specifying the phase in the lifecycle of the study site.
bridg:StudySite.statusCode
pending
bridg:StudySite.statusCode
active
bridg:StudySite.statusCode
complete
bridg:StudySite.statusCode
cancelled
bridg:StudySite.statusCode
In Review
bridg:StudySite.statusCode
Approved
bridg:StudySite.statusCode
Active
bridg:StudySite.statusCode
Closed to Accrual
bridg:StudySite.statusCode
Closed to Accrual and Intervention
bridg:StudySite.statusCode
Temporary Closed to Accrual
bridg:StudySite.statusCode
Temporary Closed to Accrual and Intervention
bridg:StudySite.statusCode
Disapproved
bridg:StudySite.statusCode
Withdrawn
bridg:StudySite.statusCode
Administratively complete.
bridg:StudySite.statusCode
The status of a study site may overlap with the study site accrual status and overall status of the study. This overlap needs to be clearly differentiated. (See tracker issue 29398). A proposed solution is to eliminate the study site accrual status codes and adopt the CTRP values for study site status code.
bridg:StudySite.statusCode
urn:C3PRv2.9:SiteStatusHistory.siteStudyStatus
bridg:StudySite.statusCode
urn:CTOM:StudySite.statusCode
bridg:StudySite.statusCode
urn:CTRPv1.0:StudyParticipation.statusCode
bridg:StudySite.statusCode
urn:CTRPv3.8:StudySiteOverallStatus.statusCode
bridg:StudySite.statusCode
urn:CTRPv3.8:FunctionalRole.statusCode
StudySiteOverallStatus
bridg:StudySite.statusCode
urn:CTRPv3.8:StudySite.
bridg:StudySite.statusCode
urn:CTRv1.0:StudySite.statusCode
bridg:StudySite.statusCode
urn:caAERSv2.2:StudySite.statusCode
bridg:StudySite.statusDate
statusDate
bridg:StudySite.statusDate
false
bridg:StudySite.statusDate
The date (and time) on which the status is assigned to the study site.
bridg:StudySite.statusDate
urn:C3PRv2.9:SiteStatusHistory.startDate
bridg:StudySite.statusDate
urn:CTOM:StudySite.irbApprovalDate
bridg:StudySite.statusDate
urn:CTRPv1.0:StudyParticipation.statusDateRange
bridg:StudySite.statusDate
urn:CTRPv3.8:StudySite.accrualDateRange
bridg:StudySite.statusDate
urn:CTRPv3.8:FunctionalRole.statusDateRange
bridg:StudySite.statusDate
urn:CTRPv3.8:StudySiteOverallStatus.statusDate
bridg:StudySite.statusDate
urn:CTRv1.0:StudySite.statusDate
bridg:StudySite.targetAccrualNumberRange
targetAccrualNumberRange
bridg:StudySite.targetAccrualNumberRange
false
bridg:StudySite.targetAccrualNumberRange
An integer falling within minimum and maximum bounds that specifies how many experimental units are needed for enrollment at this site.
bridg:StudySite.targetAccrualNumberRange
urn:C3PR:StudySite.targetAccrualNumber
bridg:StudySite.targetAccrualNumberRange
urn:C3PRv2.9:StudySite.targetAccrualNumber
bridg:StudySite.targetAccrualNumberRange
urn:CTOM:StudySite.targetAccrualNumber
bridg:StudySite.targetAccrualNumberRange
urn:CTR_Rr2:Population_planned_numbers_in_EEA
bridg:StudySite.targetAccrualNumberRange
urn:CTR_Rr2:Population_planned_numbers_in_MS
bridg:StudySite.targetAccrualNumberRange
urn:CTRPv1.0:StudyParticipation.targetAccrualNumber
bridg:StudySite.targetAccrualNumberRange
urn:CTRPv3.8:StudySite.targetAccrualNumber
bridg:StudySite.targetAccrualNumberRange
urn:CTRRr3:StudySite.targetAccrualNumberRange
bridg:StudySite.targetAccrualNumberRange
urn:CTRv1.0:StudySite.targetAccrualNumberRange
bridg:StudySiteInvestigator.identifier
identifier
bridg:StudySiteInvestigator.identifier
false
bridg:StudySiteInvestigator.identifier
A unique symbol that establishes identity of the study site investigator.
bridg:StudySiteInvestigator.identifier
Open issue: Need to know if this is actually an identifier specifically assigned to an investigator specific to a particular study and site.
bridg:StudySiteInvestigator.identifier
urn:CTRv1.0:StudySiteInvestigator.identifier
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
reviewBoardApprovalNumberText
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
false
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
A character string that is assigned by the review board upon approval of the protocol.
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:CTGOV:Board_Approval_Number
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:CTRPv3.8:StudySite.reviewBoardApprovalNumber
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:CTRR:IRB_Approval_Number
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:CTRv1.0:StudySiteOversightStatus.reviewBoardApprovalNumberText
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:HCTv1.0:MD_Anderson_Specific_Content:_Protocol_.IRB_number
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:HCTv1.0:MD_Anderson_Specific_Content:_Protocol_.IBC_number
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:HCTv1.0:MD_Anderson_Specific_Content:_Protocol_.NIH-OBA_Number
bridg:StudySiteOversightStatus.reviewBoardApprovalNumberText
urn:HSDBv1.0:[IRB].IRB_number
bridg:StudySiteOversightStatus.reviewBoardProcessCode
reviewBoardProcessCode
bridg:StudySiteOversightStatus.reviewBoardProcessCode
false
bridg:StudySiteOversightStatus.reviewBoardProcessCode
A coded value specifying the phase in the lifecycle of the review board process.
bridg:StudySiteOversightStatus.reviewBoardProcessCode
request not submitted; submitted
bridg:StudySiteOversightStatus.reviewBoardProcessCode
pending; submitted
bridg:StudySiteOversightStatus.reviewBoardProcessCode
approved; submitted
bridg:StudySiteOversightStatus.reviewBoardProcessCode
exempt; submitted
bridg:StudySiteOversightStatus.reviewBoardProcessCode
denied; submission not required
bridg:StudySiteOversightStatus.reviewBoardProcessCode
Please refer to the Review Board Process Status state transition diagram for further details.
bridg:StudySiteOversightStatus.reviewBoardProcessCode
urn:CTGOV:Board_Approval_Status
bridg:StudySiteOversightStatus.reviewBoardProcessCode
urn:CTRPv3.8:StudySite.reviewBoardApprovalStatusCode
bridg:StudySiteOversightStatus.reviewBoardProcessCode
urn:CTRR:IRB_Review/Approval_Status
bridg:StudySiteOversightStatus.reviewBoardProcessCode
urn:CTRv1.0:StudySiteOversightStatus.reviewBoardProcessCode
bridg:StudySiteOversightStatus.reviewBoardProcessCode
urn:HSDBv1.0:[IRB].IRB_review_type
bridg:StudySiteOversightStatus.reviewBoardProcessDate
reviewBoardProcessDate
bridg:StudySiteOversightStatus.reviewBoardProcessDate
false
bridg:StudySiteOversightStatus.reviewBoardProcessDate
The date (and time) on which the Institutional Review Board (IRB) determined the status of this study protocol for execution at this site.
bridg:StudySiteOversightStatus.reviewBoardProcessDate
Review Board Approval Date
bridg:StudySiteOversightStatus.reviewBoardProcessDate
urn:C3PR:StudySite.irbApprovalDate
bridg:StudySiteOversightStatus.reviewBoardProcessDate
urn:C3PRv2.9:StudySiteStudyVersion.irbApprovalDate
bridg:StudySiteOversightStatus.reviewBoardProcessDate
urn:CTOM:StudySite.irbApprovalDate
bridg:StudySiteOversightStatus.reviewBoardProcessDate
urn:CTRv1.0:StudySiteOversightStatus.reviewBoardProcessDate
bridg:StudySiteOversightStatus.reviewBoardProcessDate
urn:HSDBv1.0:[IRB].IRB_approval_date
bridg:StudySiteOversightStatus.reviewBoardProcessDate
urn:PSCv2.6:AmendmentApproval.date
bridg:StudySitePersonnel.effectiveDateRange
effectiveDateRange
bridg:StudySitePersonnel.effectiveDateRange
false
bridg:StudySitePersonnel.effectiveDateRange
The date and time span for when the study site personnel is active.
bridg:StudySitePersonnel.effectiveDateRange
urn:C3PR:HealthcareSiteInvestigator.statusDate
bridg:StudySitePersonnel.effectiveDateRange
urn:C3PR:HealthcareSiteInvestigator.statusCode
bridg:StudySitePersonnel.effectiveDateRange
urn:C3PRv2.9:StudyInvestigator.statusDate
bridg:StudySitePersonnel.effectiveDateRange
urn:C3PRv2.9:StudyInvestigator.statusCode
bridg:StudySitePersonnel.effectiveDateRange
urn:C3PRv2.9:StudyPersonnel.statusDate
bridg:StudySitePersonnel.effectiveDateRange
urn:C3PRv2.9:StudyPersonnel.statusCode
bridg:StudySitePersonnel.effectiveDateRange
urn:CTRPv1.0:StudySiteInvestigator.statusDateRange
bridg:StudySitePersonnel.effectiveDateRange
urn:CTRPv1.0:StudySiteInvestigator.statusCode
bridg:StudySitePersonnel.effectiveDateRange
urn:CTRPv1.0:StudyParticipationContact.statusDateRange
bridg:StudySitePersonnel.effectiveDateRange
urn:CTRPv1.0:StudyParticipationContact.statusCode
bridg:StudySitePersonnel.effectiveDateRange
urn:CTRPv3.8:FunctionalRole.statusDateRange
bridg:StudySitePersonnel.effectiveDateRange
urn:CTRv1.0:StudySitePersonnel.effectiveDateRange
bridg:StudySitePersonnel.effectiveDateRange
urn:caAERSv2.2:StudyPersonnel.startDate
bridg:StudySitePersonnel.effectiveDateRange
urn:caAERSv2.2:StudyPersonnel.endDate
bridg:StudySitePersonnel.postalAddress
postalAddress
bridg:StudySitePersonnel.postalAddress
false
bridg:StudySitePersonnel.postalAddress
A contact point used to send physical forms of communication to the study site personnel.
bridg:StudySitePersonnel.postalAddress
urn:CTRPv1.0:StudySiteInvestigator.postalAddress
bridg:StudySitePersonnel.postalAddress
urn:CTRPv1.0:StudyParticipationContact.postalAddress
bridg:StudySitePersonnel.postalAddress
urn:CTRPv3.8:StudySiteContact.postalAddress
bridg:StudySitePersonnel.postalAddress
urn:CTRRr3:StudySiteContact.postalAddress
bridg:StudySitePersonnel.postalAddress
urn:CTRv1.0:StudySitePersonnel.postalAddress
bridg:StudySitePersonnel.postalAddress
urn:caAERSv2.2:Address.state___SiteResearchStaff
bridg:StudySitePersonnel.postalAddress
urn:caAERSv2.2:Address.street___SiteResearchStaff
bridg:StudySitePersonnel.postalAddress
urn:caAERSv2.2:Address.country___SiteResearchStaff
bridg:StudySitePersonnel.postalAddress
urn:caAERSv2.2:Address.city___SiteResearchStaff
bridg:StudySitePersonnel.postalAddress
urn:caAERSv2.2:Address.zip___SiteResearchStaff
bridg:StudySitePersonnel.primaryIndicator
primaryIndicator
bridg:StudySitePersonnel.primaryIndicator
false
bridg:StudySitePersonnel.primaryIndicator
Specifies whether this is the main or principal study site personnel.
bridg:StudySitePersonnel.primaryIndicator
roleCode and primaryIndicator are redundant attributes when roleCode = "Principal Site Investigator" and primaryIndicator ="true".
bridg:StudySitePersonnel.primaryIndicator
urn:CTRPv1.0:StudySiteInvestigator.primaryIndicator
bridg:StudySitePersonnel.primaryIndicator
urn:CTRPv1.0:StudyParticipationContact.primaryIndicator
bridg:StudySitePersonnel.primaryIndicator
urn:CTRPv3.8:StudySiteContact.primaryIndicator
bridg:StudySitePersonnel.primaryIndicator
urn:CTRv1.0:StudySitePersonnel.primaryIndicator
bridg:StudySitePersonnel.roleCode
roleCode
bridg:StudySitePersonnel.roleCode
false
bridg:StudySitePersonnel.roleCode
The coded value specifying a type of responsibility of the study site personnel.
bridg:StudySitePersonnel.roleCode
Principal Investigator
bridg:StudySitePersonnel.roleCode
Sub Investigator
bridg:StudySitePersonnel.roleCode
Facility
bridg:StudySitePersonnel.roleCode
roleCode and primaryIndicator are redundant attributes when roleCode = "Principal Site Investigator" and primaryIndicator ="true".
bridg:StudySitePersonnel.roleCode
urn:C3PRv2.9:StudyInvestigator.roleCode
bridg:StudySitePersonnel.roleCode
urn:C3PRv2.9:RoleBasedRecipient.role
bridg:StudySitePersonnel.roleCode
urn:C3PRv2.9:StudyPersonnel.roleCode
bridg:StudySitePersonnel.roleCode
urn:CTGOV:Facility_Contact_Backup
bridg:StudySitePersonnel.roleCode
urn:CTRPv1.0:StudyParticipationContact.roleCode
bridg:StudySitePersonnel.roleCode
urn:CTRPv1.0:StudySiteInvestigator.roleCode
bridg:StudySitePersonnel.roleCode
urn:CTRPv3.8:StudySiteContact.roleCode
bridg:StudySitePersonnel.roleCode
urn:CTRR:Site_Representative/_Investigator
bridg:StudySitePersonnel.roleCode
urn:CTRv1.0:StudySitePersonnel.roleCode
bridg:StudySitePersonnel.roleCode
urn:caAERSv2.2:StudyPersonnel.roleCode
bridg:StudySitePersonnel.roleCode
urn:caAERSv2.2:RoleBasedRecipient.role
bridg:StudySitePersonnel.telecomAddress
telecomAddress
bridg:StudySitePersonnel.telecomAddress
false
bridg:StudySitePersonnel.telecomAddress
A sequence of digits or characters used to identify a particular telephone, fax, or email of a study site personnel.
bridg:StudySitePersonnel.telecomAddress
urn:CTGOV:Facility_Contact_-_Ext
bridg:StudySitePersonnel.telecomAddress
urn:CTGOV:Facility_Contact_-_Phone
bridg:StudySitePersonnel.telecomAddress
urn:CTGOV:Facility_Contact_-_Email
bridg:StudySitePersonnel.telecomAddress
urn:CTRPv1.0:StudyParticipationContact.telecomAddress
bridg:StudySitePersonnel.telecomAddress
urn:CTRPv1.0:StudySiteInvestigator.telecomAddress
bridg:StudySitePersonnel.telecomAddress
urn:CTRPv3.8:StudySiteContact.telecomAddress
bridg:StudySitePersonnel.telecomAddress
urn:CTRv1.0:StudySitePersonnel.telecomAddress
bridg:StudySitePersonnel.telecomAddress
urn:HCTv1.0:CDE_2517550:UML_DEFAULT_CD.Person_Email_Address
bridg:StudySitePersonnel.telecomAddress
urn:NCI_CRF_Standard:CDE_2661003v1.0:_Clinical_Research_Associate_Person_Telephone_Number
bridg:StudySitePersonnel.telecomAddress
urn:NCI_CRF_Standard:CDE_2661012v3.0:_Clinical_Research_Associate_Person_Fax_Number
bridg:StudySitePersonnel.telecomAddress
urn:caAERSv2.2:ContactMechanismBasedRecipient.address
bridg:StudySiteProtocolVersionRelationship.effectiveDateRange
effectiveDateRange
bridg:StudySiteProtocolVersionRelationship.effectiveDateRange
false
bridg:StudySiteProtocolVersionRelationship.effectiveDateRange
The date and time span specifying when the relationship between a study site and protocol version begins and ends.
bridg:StudySiteProtocolVersionRelationship.effectiveDateRange
urn:C3PRv2.9:StudySiteStudyVersion.endDate
bridg:StudySiteProtocolVersionRelationship.effectiveDateRange
urn:C3PRv2.9:StudySiteStudyVersion.startDate
bridg:StudySiteProtocolVersionRelationship.effectiveDateRange
urn:CTRv1.0:StudySiteProtocolVersionRelationship.effectiveDateRange
bridg:StudySiteRecruitmentStatus.code
code
bridg:StudySiteRecruitmentStatus.code
false
bridg:StudySiteRecruitmentStatus.code
A coded value specifying the phase in the lifecycle of recruitment for the study site.
bridg:StudySiteRecruitmentStatus.code
Not yet recruiting; recruiting; enrolling by invitation; active
bridg:StudySiteRecruitmentStatus.code
not recruiting; completed; suspended; terminated; withdrawn.
bridg:StudySiteRecruitmentStatus.code
The recruitment status of a study may overlap with the study site status and accrual status. This overlap needs to be clearly differentiated. (See tracker issue 29398).
bridg:StudySiteRecruitmentStatus.code
urn:C3PRv2.9:SiteStatusHistory.siteStudyStatus
bridg:StudySiteRecruitmentStatus.code
urn:CTRPv1.0:StudySiteAccrualStatus.statusCode
bridg:StudySiteRecruitmentStatus.code
urn:CTRPv3.8:StudySiteAccrualStatus.statusCode
bridg:StudySiteRecruitmentStatus.code
urn:CTRv1.0:StudySiteRecruitmentStatus.code
bridg:StudySiteRecruitmentStatus.date
date
bridg:StudySiteRecruitmentStatus.date
false
bridg:StudySiteRecruitmentStatus.date
The date (and time) on which the study site recruitment status is assigned.
bridg:StudySiteRecruitmentStatus.date
urn:C3PRv2.9:SiteStatusHistory.startDate
bridg:StudySiteRecruitmentStatus.date
urn:CTRPv1.0:StudySiteAccrualStatus.statusCode
bridg:StudySiteRecruitmentStatus.date
urn:CTRPv3.8:StudySiteAccrualStatus.statusDate
bridg:StudySiteRecruitmentStatus.date
urn:CTRv1.0:StudySiteRecruitmentStatus.date
bridg:StudySubject.confidentialityIndicator
confidentialityIndicator
bridg:StudySubject.confidentialityIndicator
false
bridg:StudySubject.confidentialityIndicator
Specifies whether the study subject, or their legally acceptable representative, has not authorized the use and disclosure of their protected health information (i.e., the study subject's data is private and confidential).
bridg:StudySubject.confidentialityIndicator
urn:CTOM:Participant.confidentialityIndicator
bridg:StudySubject.confidentialityIndicator
urn:CTRv1.0:StudySubject.confidentialityIndicator
bridg:StudySubject.paymentMethodCode
paymentMethodCode
bridg:StudySubject.paymentMethodCode
false
bridg:StudySubject.paymentMethodCode
A coded value specifying the primary payer/insurance carrier information at the time of treatment on a study.
bridg:StudySubject.paymentMethodCode
Private Insurance
bridg:StudySubject.paymentMethodCode
Medicare
bridg:StudySubject.paymentMethodCode
Medicare And Private Insurance
bridg:StudySubject.paymentMethodCode
Medicaid
bridg:StudySubject.paymentMethodCode
urn:C3PRv2.9:StudySubject.paymentMethod
bridg:StudySubject.paymentMethodCode
urn:CTOM:Participant.paymentMethodCode
bridg:StudySubject.paymentMethodCode
urn:CTRPv3.8:StudySubject.paymentMethodCode
bridg:StudySubject.paymentMethodCode
urn:CTRv1.0:StudySubject.paymentMethodCode
bridg:StudySubject.paymentMethodCode
urn:NCI_CRF_Standard:CDE_2865130v1.0:_Person_Healthcare_Payer_Type
bridg:StudySubject.statusCode
statusCode
bridg:StudySubject.statusCode
false
bridg:StudySubject.statusCode
A coded value specifying the phase in the lifecycle of the study subject.
bridg:StudySubject.statusCode
candidate
bridg:StudySubject.statusCode
eligible
bridg:StudySubject.statusCode
follow-up
bridg:StudySubject.statusCode
ineligible
bridg:StudySubject.statusCode
not registered
bridg:StudySubject.statusCode
off-study
bridg:StudySubject.statusCode
on-study
bridg:StudySubject.statusCode
pending on-study
bridg:StudySubject.statusCode
potential candidate
bridg:StudySubject.statusCode
screening
bridg:StudySubject.statusCode
withdrawn
bridg:StudySubject.statusCode
Please refer to the Study Subject Status state transition diagram for further details.
bridg:StudySubject.statusCode
urn:C3PR:StudySubject.state
bridg:StudySubject.statusCode
urn:C3PR:StudySubject.status
bridg:StudySubject.statusCode
urn:C3PRv2.9:StudySubject.regWorkflowStatus
bridg:StudySubject.statusCode
urn:CTRPv3.8:FunctionalRole.statusCode
bridg:StudySubject.statusCode
urn:CTRv1.0:StudySubject.statusCode
bridg:StudySubject.statusDate
statusDate
bridg:StudySubject.statusDate
false
bridg:StudySubject.statusDate
The date (and time) on which the status is assigned to the study subject.
bridg:StudySubject.statusDate
urn:C3PR:StudySubject.statusDateRange
bridg:StudySubject.statusDate
urn:C3PR:StudyPersonnel.endDate
bridg:StudySubject.statusDate
urn:C3PR:StudyPersonnel.startDate
bridg:StudySubject.statusDate
urn:CTRPv3.8:FunctionalRole.statusDateRange
bridg:StudySubject.statusDate
urn:CTRv1.0:StudySubject.statusDate
bridg:StudySubjectProtocolVersionRelationship.effectiveDateRange
effectiveDateRange
bridg:StudySubjectProtocolVersionRelationship.effectiveDateRange
false
bridg:StudySubjectProtocolVersionRelationship.effectiveDateRange
The date and time span specifying when the relationship between a study subject and protocol version begins and ends.
bridg:StudySubjectProtocolVersionRelationship.effectiveDateRange
urn:C3PRv2.9:StudySubjectStudyVersion
bridg:StudySubjectProtocolVersionRelationship.effectiveDateRange
urn:CTRv1.0:StudySubjectProtocolVersionRelationship.effectiveDateRange
bridg:SubjectIdentifier.effectiveDateRange
effectiveDateRange
bridg:SubjectIdentifier.effectiveDateRange
false
bridg:SubjectIdentifier.effectiveDateRange
The date (and time) span for when the subject identifier is active.
bridg:SubjectIdentifier.effectiveDateRange
urn:CTRPv1.0:IdentifiedBiologicEntity.statusCode
bridg:SubjectIdentifier.effectiveDateRange
urn:CTRPv1.0:IdentifiedBiologicEntity.statusDateRange
bridg:SubjectIdentifier.effectiveDateRange
urn:CTRv1.0:SubjectIdentifier.effectiveDateRange
bridg:SubjectIdentifier.identifier
identifier
bridg:SubjectIdentifier.identifier
false
bridg:SubjectIdentifier.identifier
A unique symbol that establishes identity of the subject.
bridg:SubjectIdentifier.identifier
study subject number 7 on a specific study
bridg:SubjectIdentifier.identifier
urn:C3PR:StudySubject.identifier
bridg:SubjectIdentifier.identifier
urn:C3PR:Identifier.value
bridg:SubjectIdentifier.identifier
urn:C3PRv2.9:Identifier.value
bridg:SubjectIdentifier.identifier
urn:CDASHv1.1:DM.USUBJID
bridg:SubjectIdentifier.identifier
urn:CDASHv1.1:DM.SUBJID
bridg:SubjectIdentifier.identifier
urn:CTOM:HealthcareSiteParticipant.participantIdentifier
bridg:SubjectIdentifier.identifier
urn:CTOM:StudyParticipantAssignment.studyParticipantIdentifier
bridg:SubjectIdentifier.identifier
urn:CTRPv3.8:StudySubject.assignedIdentifier
bridg:SubjectIdentifier.identifier
urn:CTRv1.0:SubjectIdentifier.identifier
bridg:SubjectIdentifier.identifier
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy//subject/researchSubject.id
bridg:SubjectIdentifier.identifier
urn:HCTv1.0:CDE_2729085:Specimen_Characteristics.Research_sample_donor_ID:
bridg:SubjectIdentifier.identifier
urn:HCTv1.0:CDE_2856315:Anatomic_Structure__System__or_Substance.NMDP_donor_ID:
bridg:SubjectIdentifier.identifier
urn:HCTv1.0:CDE_3118479:Medical_Records_and_Forms.CRID_processing_result:
bridg:SubjectIdentifier.identifier
urn:HCTv1.0:CDE_2889049:Anatomic_Structure__System__or_Substance.Non-NMDP_unrelated_donor_/_cord_blood_unit_ID:
in IndividualCaseSafetyReport
bridg:SubjectIdentifier.identifier
urn:ICSRr2:PrimaryRole.id
bridg:SubjectIdentifier.identifier
urn:Lab:SubjectAssignment.studySubjectIdentifier
bridg:SubjectIdentifier.identifier
urn:LabViewer2.2:Identifier.displayable
bridg:SubjectIdentifier.identifier
urn:LabViewer2.2:Identifier.extension
bridg:SubjectIdentifier.identifier
urn:LabViewer2.2:Identifier.root
bridg:SubjectIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2465308v1.0:_Patient_Multiple_Clinical_Trials_Cooperative_Group_Identifier_Number
bridg:SubjectIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2746468v1.0:_Healthcare_Facility_Participant_Identifier
bridg:SubjectIdentifier.identifier
urn:NCI_CRF_Standard:CDE_2003301v3.0:_Patient_Identifier
bridg:SubjectIdentifier.identifier
urn:PSC:StudyParticipantAssignment.studyParticipantIdentifier
bridg:SubjectIdentifier.identifier
urn:PSCv2.6:StudySubjectAssignment.studySubjectIdentifier
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:DS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:DV.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:DM.SUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:DM.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:AE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:IE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:SU.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:CO.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:MH.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:DA.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:QS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:CM.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:EX.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:LB.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:PE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:SV.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:SE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:EG.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:VS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.1:SC.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:MH.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:DS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:PC.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:DM.SUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:CE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:SU.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:QS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:EX.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:DM.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:DV.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:IE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:MB.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:FA.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:PP.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:PE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:SE.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:MS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:VS.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:SV.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:CO.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:DA.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:LB.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:SC.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:EG.USUBJID
bridg:SubjectIdentifier.identifier
urn:SDTM_IGv3.1.2:CM.USUBJID
bridg:SubjectIdentifier.identifier
urn:caAERSv2.2:StudyParticipantAssignment.studySubjectIdentifier
bridg:SubjectIdentifier.identifier
urn:caAERSv2.2:Identifier.value___Participant
bridg:SubjectIdentifier.primaryIndicator
primaryIndicator
bridg:SubjectIdentifier.primaryIndicator
false
bridg:SubjectIdentifier.primaryIndicator
Specifies whether this is the main or principal subject identifier.
bridg:SubjectIdentifier.primaryIndicator
urn:C3PRv2.9:Identifier.primaryIndicator
bridg:SubjectIdentifier.primaryIndicator
urn:CTRv1.0:SubjectIdentifier.primaryIndicator
bridg:SubjectIdentifier.primaryIndicator
urn:caAERSv2.2:Identifier.isPrimary__Participant
bridg:SubjectIdentifier.typeCode
typeCode
bridg:SubjectIdentifier.typeCode
false
bridg:SubjectIdentifier.typeCode
A coded value specifying the kind of subject identifier.
bridg:SubjectIdentifier.typeCode
study level subject identifier
bridg:SubjectIdentifier.typeCode
study site level subject identifier
bridg:SubjectIdentifier.typeCode
cross study identifier
bridg:SubjectIdentifier.typeCode
urn:AE:PersonIdentifier.identifierType
bridg:SubjectIdentifier.typeCode
urn:C3PR:Identifier.type
bridg:SubjectIdentifier.typeCode
urn:C3PRv2.9:Identifier.typeInternal
bridg:SubjectIdentifier.typeCode
urn:C3PRv2.9:OrganizationAssignedIdentifier
bridg:SubjectIdentifier.typeCode
urn:CTRPv1.0:IdentifiedBiologicEntity.typeCode
bridg:SubjectIdentifier.typeCode
urn:CTRv1.0:SubjectIdentifier.typeCode
bridg:SubjectIdentifier.typeCode
urn:caAERSv2.2:Identifier.type
bridg:SubjectIdentifier.typeCode
urn:caAERSv2.2:Identifier.type___Participant
bridg:Submission.receiptDate
receiptDate
bridg:Submission.receiptDate
true
bridg:Submission.receiptDate
The date (and time) on which the first submission unit is received by the regulatory authority.
bridg:Submission.receiptDate
Derived from the transmission of the first SubmissionUnit to a RegulatoryAuthority. The first transmission is a new SubmissionUnit, Submission and RegulatoryApplication. The first submission of a SubmissionUnit starts a regulatory clock and that is how Submission.receiptDate is derived. Subsequent SubmissionUnits are considered either amendments or supplements to the Submission and/or RegulatoryApplication and the dates for those SubmissionUnits are for tracking purposes and do not set the regulatory time clock.
bridg:Submission.receiptDate
urn:CTR_Rr2:IEC_Submission_Date
bridg:Submission.receiptDate
urn:CTR_Rr2:NCA_Submission_Date
bridg:Submission.receiptDate
urn:CTRRr3:Submission.receiptDate
bridg:Submission.receiptDate
urn:CTRv1.0:Submission.receiptDate
bridg:Submission.receiptDate
urn:RPS1:Submission.receiptDate
bridg:Submission.statusCode
statusCode
bridg:Submission.statusCode
false
bridg:Submission.statusCode
A coded value specifying the phase in the lifecycle of the submission.
bridg:Submission.statusCode
active
bridg:Submission.statusCode
withdrawn
bridg:Submission.statusCode
Please refer to the Submission Status state transition diagram for further details.
bridg:Submission.statusCode
urn:CTR_Rr2:IEC_Opinion_Status
bridg:Submission.statusCode
urn:CTR_Rr2:GMP_MP_Auth_pending
bridg:Submission.statusCode
urn:CTRv1.0:Submission.statusCode
in R_Product
bridg:Submission.statusCode
urn:ICSRr2:Approval.statusCode
bridg:Submission.statusCode
urn:RPS1:Submission.status
bridg:Submission.statusDate
statusDate
bridg:Submission.statusDate
false
bridg:Submission.statusDate
The date (and time) on which the status is assigned to the submission.
bridg:Submission.statusDate
urn:CTRv1.0:Submission.statusDate
bridg:Submission.statusDate
urn:RPS1:Submission.status
bridg:Submission.typeCode
typeCode
bridg:Submission.typeCode
false
bridg:Submission.typeCode
A coded value specifying the kind of submission.
bridg:Submission.typeCode
original
bridg:Submission.typeCode
supplement
bridg:Submission.typeCode
annual report
bridg:Submission.typeCode
urn:CTRRr3:Submission.typeCode
bridg:Submission.typeCode
urn:CTRv1.0:Submission.typeCode
bridg:Submission.typeCode
urn:RPS1:Submission.type
bridg:SubmissionUnit.effectiveDateRange
effectiveDateRange
bridg:SubmissionUnit.effectiveDateRange
false
bridg:SubmissionUnit.effectiveDateRange
The date and time span for when the submission unit is active.
bridg:SubmissionUnit.effectiveDateRange
urn:CTRv1.0:SubmissionUnit.effectiveDateRange
bridg:SubmissionUnit.effectiveDateRange
urn:RPS1:SubmissionUnit.status
bridg:SubmissionUnit.effectiveDateRange
urn:RPS1:ReviewableUnit.status
bridg:SubmissionUnit.receiptDate
receiptDate
bridg:SubmissionUnit.receiptDate
false
bridg:SubmissionUnit.receiptDate
The date (and time) on which the submission unit is received by the regulatory authority.
bridg:SubmissionUnit.receiptDate
Typically, this date will start a review clock, if applicable. The combination of the typeCode and where the SubmissionUnit was received will determine the deadline for the SubmissionUnit to be reviewed.
bridg:SubmissionUnit.receiptDate
urn:CTRv1.0:SubmissionUnit.receiptDate
bridg:SubmissionUnit.receiptDate
urn:RPS1:SubmissionUnit.receiptDate
bridg:SubmissionUnit.typeCode
typeCode
bridg:SubmissionUnit.typeCode
false
bridg:SubmissionUnit.typeCode
A coded value specifying the kind of submission unit.
bridg:SubmissionUnit.typeCode
original
bridg:SubmissionUnit.typeCode
amendment
bridg:SubmissionUnit.typeCode
supplement
bridg:SubmissionUnit.typeCode
Typically each submission unit type would cause a different regulatory request.
bridg:SubmissionUnit.typeCode
urn:CTRv1.0:SubmissionUnit.typeCode
bridg:SubmissionUnit.typeCode
urn:RPS1:SubmissionUnit.type
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
donorTypeCode
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
false
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
A coded value specifying the kind of donor that is used.
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
Syngeneic
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
HLA-identical sibling
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
HLA-matched other relative
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
HLA-mismatched relative
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
Unrelated donor
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
urn:HCTv1.0:CDE_2730901:Therapy_Doses.What_source_was_used_for_the_hematopoietic_stem_cell_transplantation?
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
urn:HCTv1.0:CDE_2889035:Anatomic_Structure__System__or_Substance.What_kind_of_non-NMDP_donor_type_is_it?
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
urn:HCTv1.0:CDE_2730905:Therapy_Doses.Was_a_particular_hematopoietic_stem_cell_source_used?
HSCT : Part 1 of 4.If there has been more than one hematopoietic stem cell transplantation, what was the type of the most recent previous hematopoietic stem cell transplantation?
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
urn:HCTv1.0:CDE_2675073:Hematopoietic_Stem_Cell_Transplant
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
urn:HCTv1.0:CDE_2897753:Anatomic_Structure__System__or_Substance.Specify_tissue_donor_type:
bridg:SubstanceExtractionAdministrationRelationship.donorTypeCode
urn:HCTv1.0:CDE_2675075:DONOR'.What_type_of_donor_was_used_for_this_hematopoietic_stem_cell_transplant?
bridg:SubstanceExtractionAdministrationRelationship.relationCode
relationCode
bridg:SubstanceExtractionAdministrationRelationship.relationCode
false
bridg:SubstanceExtractionAdministrationRelationship.relationCode
A coded value specifying the self-relationship of the source to the target.
bridg:SubstanceExtractionAdministrationRelationship.relationCode
Autologous (self)
bridg:SubstanceExtractionAdministrationRelationship.relationCode
Allogeneic-related
bridg:SubstanceExtractionAdministrationRelationship.relationCode
Allogeneic Unrelated
bridg:SubstanceExtractionAdministrationRelationship.relationCode
This is not a familial relationship.
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:CDE_2771526:Therapies.What_was_the_HSC_source?
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:CDE_2761889:DONOR'.Autologous_HSCT?
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Allogeneic
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:MD_Anderson_Specific_Content:_Product.Autologous_product
were the prior HSC source(s?
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:CDE_2957396:Therapy_Doses.What_was
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:CDE_2815342:Therapies.What_is_the_subsequent_HSCT_transplant_type?
bridg:SubstanceExtractionAdministrationRelationship.relationCode
urn:HCTv1.0:CDE_2957417:Techniques.What_was_the_HSC_source_for_the_last_HSCT?
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
reasonCode
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
false
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
A coded value specifying the motivation, cause, or rationale for the supplemental statistical analysis plan.
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
Additional analyses during clinical study report preparation
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
Response to regulatory request
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
Hypothesis generation
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
This coded concept is extensible, but the examples above cover a large proportion of possible values.
bridg:SupplementalStatisticalAnalysisPlanVersion.reasonCode
urn:Statistics_v1.0:SupplementalStatisticalAnalysisPlanVersion.reasonCode
bridg:SystemOfRecord.name
name
bridg:SystemOfRecord.name
false
bridg:SystemOfRecord.name
A non-unique textual identifier for the system that assigned the identifier.
bridg:SystemOfRecord.name
urn:C3PRv2.9:SystemAssignedIdentifier.systemName
bridg:SystemOfRecord.name
urn:CTRv1.0:SystemOfRecord.name
bridg:SystemOfRecord.name
urn:caAERSv2.2:SystemAssignedIdentifier.systemName
bridg:TargetAnatomicSite.code
code
bridg:TargetAnatomicSite.code
false
bridg:TargetAnatomicSite.code
A coded value specifying the anatomic location that is the focus of an observation result.
bridg:TargetAnatomicSite.code
arm for skin rash.
bridg:TargetAnatomicSite.code
brain stem or spinal cord for a lesion
bridg:TargetAnatomicSite.code
The target site of the result may be different than the target site of the activity (PerformedObservation) that generated it. For example, a chest x-ray (observation) has the target site of chest while the result might show an infiltration in the left lower lobe of the lung (target site of result), or a dermatological exam may check the skin across the whole body (target site of observation) while the result might identify a rash on the right leg (target site of result).
Sources that capture anatomic site and laterality separately should map both to this attribute. For implementation models based on BRIDG where site and laterality are captured separately, you may wish to capture both concepts as a post-coordinated code structure or as multiple code repetitions.
bridg:TargetAnatomicSite.code
urn:AE:AdverseEvent.bodyLocation
bridg:TargetAnatomicSite.code
urn:C3PRv2.9:ICD9DiseaseSite.name
bridg:TargetAnatomicSite.code
urn:C3PRv2.9:ICD9DiseaseSite.code
bridg:TargetAnatomicSite.code
urn:C3PRv2.9:ICD9DiseaseSite
bridg:TargetAnatomicSite.code
urn:C3PRv2.9:DiseaseHistory.otherPrimaryDiseaseSiteCode
bridg:TargetAnatomicSite.code
urn:CTOM:Diagnosis.primaryAnatomicSiteLateralityCode
bridg:TargetAnatomicSite.code
urn:CTOM:Diagnosis.primaryAnatomicSiteCodeSystem
bridg:TargetAnatomicSite.code
urn:CTOM:LesionDescription.anatomicSiteCode
bridg:TargetAnatomicSite.code
urn:CTOM:LesionDescription.anatomicSiteCodeSystem
bridg:TargetAnatomicSite.code
urn:CTOM:Diagnosis.primaryAnatomicSiteCode
bridg:TargetAnatomicSite.code
urn:CTRv1.0:PerformedObservationResult.targetAnatomicSiteCode
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2986153:Anatomic_Sites.Specify_site_of_extra-gonadal_germ_cell_tumor:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2739572:Disease__Disorder_or_Finding.Specify_other_extramedullary_diease_site
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_65154_/:Involvement_and_Extent_of_Disease.Site_of_Involvement
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2967296:Anatomic_Sites.Specify_other_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2739560:Disease__Disorder_or_Finding.Specify_extramedullary_diease_site_type:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2971708:Disease_Response.Which_site?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2793731:Anatomic_Sites.Specify_the_other_site_of_the_organ_involvement:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2969634:Involvement_and_Extent_of_Disease.Specify_other_metastasis_lymph_nodes:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2987033:Anatomic_Sites.What_was_the_site_of_the_extragonadal_germ_cell_metastases?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2787385:Anatomic_Sites.Specify_the_biopsy_site_used_to_indicate_the_diagnostic_evidence:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2970480:Lab_Results.Specify_other_tissue:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3020048:Disease__Disorder_or_Finding.Specify_location_of_the_central_nervous_system_abnormalities:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2969616:Lab_Results.What_biopsy_site_was_positive_for_neuroblastoma?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2986193:Anatomic_Sites.Specify_tumor_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2003987:Anatomic_Sites.Body_Site
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2962064:Anatomic_Sites.What_was_the_primary_CNS_tumor_site_?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2970615:Involvement_and_Extent_of_Disease.Specify_other_sites:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3133376:Involvement_and_Extent_of_Disease.What_is_the_disease_involvment_site_name?
s of disease progression / recurrence:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3031379:Anatomic_Sites.Specify_the_known_site
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3057312:Anatomic_Sites.On_what_eye_was_the_examination_performed?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2970440:Lab_Results.What_tissues_were_analyzed?
s of relapse/progression:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2978277:Anatomic_Sites.Specify_site
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2961431:Involvement_and_Extent_of_Disease.Specify_metastasis_anatomic_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3005935:Involvement_and_Extent_of_Disease.Specify_amyloidosis_other_system_response:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3124482:Anatomic_Sites.Specify_other_site:
s of active leukemia:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2760980:Disease__Disorder_or_Finding.Specify_site
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3009313:Anatomic_Sites.Specify_other_organ_system_assessed_for_status:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_61294//:Anatomic_Sites.Other_specify
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2974004:Disease_Response.Specify_other_site:_
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2761018:Disease__Disorder_or_Finding.Speficy_the_location_of_active_leukemia_in_the_patient:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2873907:Disease__Disorder_or_Finding.Second_infectious_disorder_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2760036:Diagnosis.Indicate_the_site_the_hemorrhage_occurred:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2767//P:Anatomic_Sites.Is_the_primary_site_or_tumor_bed_involved
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2873912:Disease__Disorder_or_Finding.Third_infectious_disorder_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3124480:Anatomic_Sites.Which_sites_of_neuroblastoma_were_involved?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2969604:Anatomic_Sites.What_was_the_location_of_the_breast_cancer?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2962066:Anatomic_Sites.Specify_other_primary_CNS_tumor_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2969639:Lab_Results.What_was_the_other_biopsy_site_positive_for_neuroblastoma?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2987074:Anatomic_Sites.Specify_other_site_extra-gonadal_metastases_present:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2967298:Diagnosis.What_was_the_site_of_metastasis?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2970680:Anatomic_Sites.What_was_the_site_of_disease_involvement?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3082348:Involvement_and_Extent_of_Disease.What_was_the_site_of_extranodal_involvement?
s of primary tumors(s:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3086004:Anatomic_Sites.Specify_the_site
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2969632:Anatomic_Sites.Which_sites_did_the_metastasis_lymph_nodes_present?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2787340:Anatomic_Sites.What_is_the_biopsy_site_used_to_indicate_the_diagnostic_evidence:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_3061535:Diagnosis.Specify_the_site_of_metastasis:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2793699:Anatomic_Sites.Specify_the_site_of_the_organ_involvement:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2952465:Anatomic_Sites.Extranodal_involvement_anatomic_site_specify:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2871915:Disease__Disorder_or_Finding.First_infectious_disorder_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2760031:Diagnosis.What_is_the_hemorrhage_site?
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2934832:Anatomic_Sites.Select_the_infection_organism_site:
bridg:TargetAnatomicSite.code
urn:HCTv1.0:CDE_2970368:Lab_Results.Specify_the_tissue_analyzed:
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.1:AE.AELOC
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.1:PE.PELOC
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.1:EX.EXLOC
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.1:VS.VSLOC
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.2:FA.FALOC
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.2:PE.PELOC
bridg:TargetAnatomicSite.code
urn:SDTM_IGv3.1.2:AE.AELOC
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:MetastaticDiseaseSite___DiseaseHistory
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:MetastaticDiseaseSite.otherSite___DiseaseHistory
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:StudyParticipantDiseaseHistory.otherPrimaryDiseaseSite
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:MetastaticDiseaseSite
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:DiseaseHistory.otherPrimaryDiseaseSite
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:AnatomicSite.name___StudyParticipationDiseaseHistory
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:MetastaticDiseaseSite.otherSite___StudyParticipantDiseaseHistory
bridg:TargetAnatomicSite.code
urn:caAERSv2.2:AnatomicSite.name___DiseaseHistory
bridg:TargetAnatomicSite.primaryIndicator
primaryIndicator
bridg:TargetAnatomicSite.primaryIndicator
false
bridg:TargetAnatomicSite.primaryIndicator
Specifies whether this is the main or principal site.
bridg:Activity.involvedExperimentalUnit
be participated in by
bridg:Activity.involvedExperimentalUnit
none
bridg:Activity.involvedExperimentalUnit
involvedExperimentalUnit
bridg:Activity.involvedExperimentalUnit
false
bridg:Activity.involvedExperimentalUnit
ExperimentalUnit
bridg:Activity.involvedExperimentalUnit
urn:CTRRr3:Activity.involved
ExperimentalUnit
bridg:Activity.involvedExperimentalUnit
urn:CTRv1.0:Activity.involved
bridg:ExperimentalUnit.involvingActivity
participate in
bridg:ExperimentalUnit.involvingActivity
none
bridg:ExperimentalUnit.involvingActivity
involvingActivity
bridg:Activity.involvedSubject
be participated in by
bridg:Activity.involvedSubject
none
bridg:Activity.involvedSubject
involvedSubject
bridg:Activity.involvedSubject
false
bridg:Activity.involvedSubject
Activity
bridg:Activity.involvedSubject
urn:CTRPv3.8:StudySubject.
Arm
bridg:Activity.involvedSubject
urn:CTRv1.0:StudySubject.intended
Subject
bridg:Activity.involvedSubject
urn:CTRv1.0:Activity.involved
bridg:Subject.involvingActivity
participate in
bridg:Subject.involvingActivity
none
bridg:Subject.involvingActivity
involvingActivity
bridg:AdministrativeMemberCRA.performingResearchStaff
is a function performed by
bridg:AdministrativeMemberCRA.performingResearchStaff
none
bridg:AdministrativeMemberCRA.performingResearchStaff
performingResearchStaff
bridg:AdministrativeMemberCRA.performingResearchStaff
false
bridg:AdministrativeMemberCRA.performingResearchStaff
bridg:ResearchStaff.performedAdministrativeMemberCRA
function as
bridg:ResearchStaff.performedAdministrativeMemberCRA
none
bridg:ResearchStaff.performedAdministrativeMemberCRA
performedAdministrativeMemberCRA
bridg:AdministrativeMemberCRA.staffedCooperativeGroupMember
staffs
bridg:AdministrativeMemberCRA.staffedCooperativeGroupMember
none
bridg:AdministrativeMemberCRA.staffedCooperativeGroupMember
staffedCooperativeGroupMember
bridg:AdministrativeMemberCRA.staffedCooperativeGroupMember
false
bridg:AdministrativeMemberCRA.staffedCooperativeGroupMember
bridg:CooperativeGroupMember.staffingAdministrativeMemberCRA
is staffed by
bridg:CooperativeGroupMember.staffingAdministrativeMemberCRA
none
bridg:CooperativeGroupMember.staffingAdministrativeMemberCRA
staffingAdministrativeMemberCRA
bridg:AdministrativeMemberPI.performingResearchStaff
is a function performed by
bridg:AdministrativeMemberPI.performingResearchStaff
none
bridg:AdministrativeMemberPI.performingResearchStaff
performingResearchStaff
bridg:AdministrativeMemberPI.performingResearchStaff
false
bridg:AdministrativeMemberPI.performingResearchStaff
bridg:ResearchStaff.performedAdministrativeMemberPI
function as
bridg:ResearchStaff.performedAdministrativeMemberPI
none
bridg:ResearchStaff.performedAdministrativeMemberPI
performedAdministrativeMemberPI
bridg:AdministrativeMemberPI.staffedCooperativeGroupMember
staffs
bridg:AdministrativeMemberPI.staffedCooperativeGroupMember
none
bridg:AdministrativeMemberPI.staffedCooperativeGroupMember
staffedCooperativeGroupMember
bridg:AdministrativeMemberPI.staffedCooperativeGroupMember
false
bridg:AdministrativeMemberPI.staffedCooperativeGroupMember
bridg:CooperativeGroupMember.staffingAdministrativeMemberPI
is staffed by
bridg:CooperativeGroupMember.staffingAdministrativeMemberPI
none
bridg:CooperativeGroupMember.staffingAdministrativeMemberPI
staffingAdministrativeMemberPI
bridg:AdverseEventOutcomeAssessment.triggeringAdverseEvent
is triggered by
bridg:AdverseEventOutcomeAssessment.triggeringAdverseEvent
none
bridg:AdverseEventOutcomeAssessment.triggeringAdverseEvent
triggeringAdverseEvent
bridg:AdverseEventOutcomeAssessment.triggeringAdverseEvent
false
bridg:AdverseEventOutcomeAssessment.triggeringAdverseEvent
AdverseEvent
bridg:AdverseEventOutcomeAssessment.triggeringAdverseEvent
urn:CTRv1.0:AdverseEventOutcomeAssessment.triggering
bridg:AdverseEvent.triggeredAdverseEventOutcomeAssessment
trigger
bridg:AdverseEvent.triggeredAdverseEventOutcomeAssessment
none
bridg:AdverseEvent.triggeredAdverseEventOutcomeAssessment
triggeredAdverseEventOutcomeAssessment
bridg:AdverseEventSeriousness.describedAdverseEvent
describes
bridg:AdverseEventSeriousness.describedAdverseEvent
none
bridg:AdverseEventSeriousness.describedAdverseEvent
describedAdverseEvent
bridg:AdverseEventSeriousness.describedAdverseEvent
false
bridg:AdverseEventSeriousness.describedAdverseEvent
AdverseEvent
bridg:AdverseEventSeriousness.describedAdverseEvent
urn:CTRv1.0:AdverseEventSeriousness.described
bridg:AdverseEvent.describingAdverseEventSeriousness
be described by
bridg:AdverseEvent.describingAdverseEventSeriousness
none
bridg:AdverseEvent.describingAdverseEventSeriousness
describingAdverseEventSeriousness
bridg:Arm.containedPlannedActivity
contains
bridg:Arm.containedPlannedActivity
none
bridg:Arm.containedPlannedActivity
containedPlannedActivity
bridg:Arm.containedPlannedActivity
false
bridg:Arm.containedPlannedActivity
ArmIntervention
bridg:Arm.containedPlannedActivity
urn:CTRPv3.8:PlannedActivity.
ArmIntervention
bridg:Arm.containedPlannedActivity
urn:CTRPv3.8:Arm.
Arm
bridg:Arm.containedPlannedActivity
urn:CTRRr3:PlannedActivity.containing
Arm
bridg:Arm.containedPlannedActivity
urn:CTRv1.0:PlannedActivity.containing
bridg:PlannedActivity.containingArm
occur in
bridg:PlannedActivity.containingArm
none
bridg:PlannedActivity.containingArm
containingArm
bridg:Arm.subdividedStudyProtocolVersion
is a division of
bridg:Arm.subdividedStudyProtocolVersion
none
bridg:Arm.subdividedStudyProtocolVersion
subdividedStudyProtocolVersion
bridg:Arm.subdividedStudyProtocolVersion
false
bridg:Arm.subdividedStudyProtocolVersion
bridg:Arm.subdividedStudyProtocolVersion
urn:CTRPv1.0:ObservationalStudyProtocol.groupNumber
Arm
bridg:Arm.subdividedStudyProtocolVersion
urn:CTRPv3.8:StudyProtocol.
Study
bridg:Arm.subdividedStudyProtocolVersion
urn:CTRRr3:Arm.subdivided
StudyProtocolVersion
bridg:Arm.subdividedStudyProtocolVersion
urn:CTRv1.0:Arm.subdivided
bridg:StudyProtocolVersion.subdividingArm
be divided into
bridg:StudyProtocolVersion.subdividingArm
none
bridg:StudyProtocolVersion.subdividingArm
subdividingArm
bridg:AssessedActivityRelationship.assessedPerformedActivity
has as subject
bridg:AssessedActivityRelationship.assessedPerformedActivity
none
bridg:AssessedActivityRelationship.assessedPerformedActivity
assessedPerformedActivity
bridg:AssessedActivityRelationship.assessedPerformedActivity
false
bridg:AssessedActivityRelationship.assessedPerformedActivity
bridg:PerformedActivity.assessingAssessedActivityRelationship
be the subject of
bridg:PerformedActivity.assessingAssessedActivityRelationship
none
bridg:PerformedActivity.assessingAssessedActivityRelationship
assessingAssessedActivityRelationship
bridg:AssessedActivityRelationship.assessingPerformedObservation
is the subject of
bridg:AssessedActivityRelationship.assessingPerformedObservation
none
bridg:AssessedActivityRelationship.assessingPerformedObservation
assessingPerformedObservation
bridg:AssessedActivityRelationship.assessingPerformedObservation
false
bridg:AssessedActivityRelationship.assessingPerformedObservation
bridg:PerformedObservation.assessedAssessedActivityRelationship
have as subject
bridg:PerformedObservation.assessedAssessedActivityRelationship
none
bridg:PerformedObservation.assessedAssessedActivityRelationship
assessedAssessedActivityRelationship
bridg:AssessedResultRelationship.assessedPerformedObservationResult
has as subject
bridg:AssessedResultRelationship.assessedPerformedObservationResult
none
bridg:AssessedResultRelationship.assessedPerformedObservationResult
assessedPerformedObservationResult
bridg:AssessedResultRelationship.assessedPerformedObservationResult
false
bridg:AssessedResultRelationship.assessedPerformedObservationResult
PerformedObservationResult
bridg:AssessedResultRelationship.assessedPerformedObservationResult
urn:CTRv1.0:AssessedResultRelationship.assessed
bridg:PerformedObservationResult.assessingAssessedResultRelationship
be the subject of
bridg:PerformedObservationResult.assessingAssessedResultRelationship
none
bridg:PerformedObservationResult.assessingAssessedResultRelationship
assessingAssessedResultRelationship
bridg:AssessedResultRelationship.assessingPerformedObservation
is the subject of
bridg:AssessedResultRelationship.assessingPerformedObservation
none
bridg:AssessedResultRelationship.assessingPerformedObservation
assessingPerformedObservation
bridg:AssessedResultRelationship.assessingPerformedObservation
false
bridg:AssessedResultRelationship.assessingPerformedObservation
PerformedObservation
bridg:AssessedResultRelationship.assessingPerformedObservation
urn:CTRv1.0:AssessedResultRelationship.assessing
bridg:PerformedObservation.assessedAssessedResultRelationship
have as subject
bridg:PerformedObservation.assessedAssessedResultRelationship
none
bridg:PerformedObservation.assessedAssessedResultRelationship
assessedAssessedResultRelationship
bridg:Assessor.performingAssociatedBiologicEntity
be a function performed by
bridg:Assessor.performingAssociatedBiologicEntity
none
bridg:Assessor.performingAssociatedBiologicEntity
performingAssociatedBiologicEntity
bridg:Assessor.performingAssociatedBiologicEntity
false
bridg:Assessor.performingAssociatedBiologicEntity
AssociatedBiologicEntity
bridg:Assessor.performingAssociatedBiologicEntity
urn:CTRv1.0:Assessor.performing
bridg:AssociatedBiologicEntity.performedAssessor
function as
bridg:AssociatedBiologicEntity.performedAssessor
none
bridg:AssociatedBiologicEntity.performedAssessor
performedAssessor
bridg:Assessor.performingDevice
be a function performed by
bridg:Assessor.performingDevice
none
bridg:Assessor.performingDevice
performingDevice
bridg:Assessor.performingDevice
false
bridg:Assessor.performingDevice
Device
bridg:Assessor.performingDevice
urn:CTRv1.0:Assessor.performing
bridg:Device.performedAssessor
function as
bridg:Device.performedAssessor
none
bridg:Device.performedAssessor
performedAssessor
bridg:Assessor.performingHealthcareProvider
be a function performed by
bridg:Assessor.performingHealthcareProvider
none
bridg:Assessor.performingHealthcareProvider
performingHealthcareProvider
bridg:Assessor.performingHealthcareProvider
false
bridg:Assessor.performingHealthcareProvider
HealthcareProvider
bridg:Assessor.performingHealthcareProvider
urn:CTRv1.0:Assessor.performing
bridg:HealthcareProvider.performedAssessor
function as
bridg:HealthcareProvider.performedAssessor
none
bridg:HealthcareProvider.performedAssessor
performedAssessor
bridg:Assessor.performingLaboratory
be a function performed by
bridg:Assessor.performingLaboratory
none
bridg:Assessor.performingLaboratory
performingLaboratory
bridg:Assessor.performingLaboratory
false
bridg:Assessor.performingLaboratory
bridg:Laboratory.performedAssessor
function as
bridg:Laboratory.performedAssessor
none
bridg:Laboratory.performedAssessor
performedAssessor
bridg:Assessor.performingOversightCommittee
be a function performed by
bridg:Assessor.performingOversightCommittee
none
bridg:Assessor.performingOversightCommittee
performingOversightCommittee
bridg:Assessor.performingOversightCommittee
false
bridg:Assessor.performingOversightCommittee
OversightCommittee
bridg:Assessor.performingOversightCommittee
urn:CTRv1.0:Assessor.performing
bridg:OversightCommittee.performedAssessor
function as
bridg:OversightCommittee.performedAssessor
none
bridg:OversightCommittee.performedAssessor
performedAssessor
bridg:Assessor.performingResearchStaff
be a function performed by
bridg:Assessor.performingResearchStaff
none
bridg:Assessor.performingResearchStaff
performingResearchStaff
bridg:Assessor.performingResearchStaff
false
bridg:Assessor.performingResearchStaff
ResearchStaff
bridg:Assessor.performingResearchStaff
urn:CTRv1.0:Assessor.performing
bridg:ResearchStaff.performedAssessor
function as
bridg:ResearchStaff.performedAssessor
none
bridg:ResearchStaff.performedAssessor
performedAssessor
bridg:Assessor.performingSubject
be a function performed by
bridg:Assessor.performingSubject
none
bridg:Assessor.performingSubject
performingSubject
bridg:Assessor.performingSubject
false
bridg:Assessor.performingSubject
Subject
bridg:Assessor.performingSubject
urn:CTRv1.0:Assessor.performing
bridg:Subject.performedAssessor
function as
bridg:Subject.performedAssessor
none
bridg:Subject.performedAssessor
performedAssessor
bridg:AssociatedBiologicEntity.performingBiologicEntity
is a function performed by
bridg:AssociatedBiologicEntity.performingBiologicEntity
none
bridg:AssociatedBiologicEntity.performingBiologicEntity
performingBiologicEntity
bridg:AssociatedBiologicEntity.performingBiologicEntity
false
bridg:AssociatedBiologicEntity.performingBiologicEntity
BiologicEntity
bridg:AssociatedBiologicEntity.performingBiologicEntity
urn:CTRv1.0:AssociatedBiologicEntity.performing
bridg:BiologicEntity.performedAssociatedBiologicEntity
function as
bridg:BiologicEntity.performedAssociatedBiologicEntity
none
bridg:BiologicEntity.performedAssociatedBiologicEntity
performedAssociatedBiologicEntity
bridg:AssociatedBiologicEntity.scopingBiologicEntity
is scoped by
bridg:AssociatedBiologicEntity.scopingBiologicEntity
none
bridg:AssociatedBiologicEntity.scopingBiologicEntity
scopingBiologicEntity
bridg:AssociatedBiologicEntity.scopingBiologicEntity
false
bridg:AssociatedBiologicEntity.scopingBiologicEntity
BiologicEntity
bridg:AssociatedBiologicEntity.scopingBiologicEntity
urn:CTRv1.0:AssociatedBiologicEntity.scoping
bridg:BiologicEntity.scopedAssociatedBiologicEntity
scope
bridg:BiologicEntity.scopedAssociatedBiologicEntity
none
bridg:BiologicEntity.scopedAssociatedBiologicEntity
scopedAssociatedBiologicEntity
bridg:BiologicEntityGroup.containingBiologicEntityGroup
contain
bridg:BiologicEntityGroup.containingBiologicEntityGroup
none
bridg:BiologicEntityGroup.containingBiologicEntityGroup
containingBiologicEntityGroup
bridg:BiologicEntityGroup.containingBiologicEntityGroup
false
bridg:BiologicEntityGroup.containingBiologicEntityGroup
Indicates that one biologic entity group is composed of other groups.
bridg:BiologicEntityGroup.containingBiologicEntityGroup
Allows scenarios such as barn with stalls with crates of chickens - different therapies or observations might be made at different levels of grouping.
DEFINITION:
Indicates that one biologic entity group is composed of other groups.
EXAMPLE(S):
OTHER NAME(S):
NOTE(S):
bridg:BiologicEntityGroup.containedBiologicEntityGroup
be contained in
bridg:BiologicEntityGroup.containedBiologicEntityGroup
none
bridg:BiologicEntityGroup.containedBiologicEntityGroup
containedBiologicEntityGroup
bridg:BiologicEntityGroup.groupedBiologicEntity
groups
bridg:BiologicEntityGroup.groupedBiologicEntity
shared
bridg:BiologicEntityGroup.groupedBiologicEntity
groupedBiologicEntity
bridg:BiologicEntityGroup.groupedBiologicEntity
false
bridg:BiologicEntityGroup.groupedBiologicEntity
BiologicEntity
bridg:BiologicEntityGroup.groupedBiologicEntity
urn:CTRv1.0:BiologicEntityGroup.grouped
bridg:BiologicEntity.groupingBiologicEntityGroup
be grouped by
bridg:BiologicEntity.groupingBiologicEntityGroup
none
bridg:BiologicEntity.groupingBiologicEntityGroup
groupingBiologicEntityGroup
bridg:BiologicEntityIdentifier.assigningOrganization
be assigned by
bridg:BiologicEntityIdentifier.assigningOrganization
none
bridg:BiologicEntityIdentifier.assigningOrganization
assigningOrganization
bridg:BiologicEntityIdentifier.assigningOrganization
false
bridg:BiologicEntityIdentifier.assigningOrganization
Organization
bridg:BiologicEntityIdentifier.assigningOrganization
urn:CTRRr3:BiologicEntityIdentifier.assigning
Organization
bridg:BiologicEntityIdentifier.assigningOrganization
urn:CTRv1.0:BiologicEntityIdentifier.assigning
bridg:Organization.assignedBiologicEntityIdentifier
assign
bridg:Organization.assignedBiologicEntityIdentifier
none
bridg:Organization.assignedBiologicEntityIdentifier
assignedBiologicEntityIdentifier
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
identifies
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
none
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
identifiedBiologicEntity
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
false
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
IdentifiedEntity
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
urn:CTRPv3.8:Person.
BiologicEntity
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
urn:CTRRr3:BiologicEntityIdentifier.identified
BiologicEntity
bridg:BiologicEntityIdentifier.identifiedBiologicEntity
urn:CTRv1.0:BiologicEntityIdentifier.identified
bridg:BiologicEntity.identifyingBiologicEntityIdentifier
be identified by
bridg:BiologicEntity.identifyingBiologicEntityIdentifier
none
bridg:BiologicEntity.identifyingBiologicEntityIdentifier
identifyingBiologicEntityIdentifier
bridg:BiologicEntityPart.containingBiologicEntity
is part of
bridg:BiologicEntityPart.containingBiologicEntity
none
bridg:BiologicEntityPart.containingBiologicEntity
containingBiologicEntity
bridg:BiologicEntityPart.containingBiologicEntity
false
bridg:BiologicEntityPart.containingBiologicEntity
BiologicEntity
bridg:BiologicEntityPart.containingBiologicEntity
urn:CTRRr3:BiologicEntityPart.containing
BiologicEntity
bridg:BiologicEntityPart.containingBiologicEntity
urn:CTRv1.0:BiologicEntityPart.containing
bridg:BiologicEntity.containedBiologicEntityPart
have
bridg:BiologicEntity.containedBiologicEntityPart
none
bridg:BiologicEntity.containedBiologicEntityPart
containedBiologicEntityPart
bridg:CausalAssessment.triggeringAdverseEvent
is triggered by
bridg:CausalAssessment.triggeringAdverseEvent
none
bridg:CausalAssessment.triggeringAdverseEvent
triggeringAdverseEvent
bridg:CausalAssessment.triggeringAdverseEvent
false
bridg:CausalAssessment.triggeringAdverseEvent
AdverseEvent
bridg:CausalAssessment.triggeringAdverseEvent
urn:CTRv1.0:CausalAssessment.triggering
bridg:AdverseEvent.triggeredCausalAssessment
trigger
bridg:AdverseEvent.triggeredCausalAssessment
none
bridg:AdverseEvent.triggeredCausalAssessment
triggeredCausalAssessment
bridg:CollectingLaboratory.performingLaboratory
is a function performed by
bridg:CollectingLaboratory.performingLaboratory
none
bridg:CollectingLaboratory.performingLaboratory
performingLaboratory
bridg:CollectingLaboratory.performingLaboratory
false
bridg:CollectingLaboratory.performingLaboratory
Laboratory
bridg:CollectingLaboratory.performingLaboratory
urn:CTRv1.0:CollectingLaboratory.performing
bridg:Laboratory.performedCollectingLaboratory
function as
bridg:Laboratory.performedCollectingLaboratory
none
bridg:Laboratory.performedCollectingLaboratory
performedCollectingLaboratory
bridg:CompanionStudyRelationship.accompaniedStudyProtocolVersion
is a companion of
bridg:CompanionStudyRelationship.accompaniedStudyProtocolVersion
none
bridg:CompanionStudyRelationship.accompaniedStudyProtocolVersion
accompaniedStudyProtocolVersion
bridg:CompanionStudyRelationship.accompaniedStudyProtocolVersion
false
bridg:CompanionStudyRelationship.accompaniedStudyProtocolVersion
StudyProtocolVersion
bridg:CompanionStudyRelationship.accompaniedStudyProtocolVersion
urn:CTRv1.0:CompanionStudyRelationship.accompanied
bridg:StudyProtocolVersion.accompanyingCompanionStudyRelationship
have as a companion
bridg:StudyProtocolVersion.accompanyingCompanionStudyRelationship
none
bridg:StudyProtocolVersion.accompanyingCompanionStudyRelationship
accompanyingCompanionStudyRelationship
bridg:CompanionStudyRelationship.accompanyingStudyProtocol
has as a companion
bridg:CompanionStudyRelationship.accompanyingStudyProtocol
none
bridg:CompanionStudyRelationship.accompanyingStudyProtocol
accompanyingStudyProtocol
bridg:CompanionStudyRelationship.accompanyingStudyProtocol
false
bridg:CompanionStudyRelationship.accompanyingStudyProtocol
StudyProtocol
bridg:CompanionStudyRelationship.accompanyingStudyProtocol
urn:CTRv1.0:CompanionStudyRelationship.accompanying
bridg:StudyProtocol.accompaniedCompanionStudyRelationship
be a companion of
bridg:StudyProtocol.accompaniedCompanionStudyRelationship
none
bridg:StudyProtocol.accompaniedCompanionStudyRelationship
accompaniedCompanionStudyRelationship
bridg:ConcomitantAgent.performingProduct
is a function performed by
bridg:ConcomitantAgent.performingProduct
none
bridg:ConcomitantAgent.performingProduct
performingProduct
bridg:ConcomitantAgent.performingProduct
false
bridg:ConcomitantAgent.performingProduct
Product
bridg:ConcomitantAgent.performingProduct
urn:CTRv1.0:ConcomitantAgent.performing
bridg:Product.performedConcomitantAgent
function as
bridg:Product.performedConcomitantAgent
none
bridg:Product.performedConcomitantAgent
performedConcomitantAgent
bridg:ConcomitantAgent.usingPerformedProcedure
is used during
bridg:ConcomitantAgent.usingPerformedProcedure
none
bridg:ConcomitantAgent.usingPerformedProcedure
usingPerformedProcedure
bridg:ConcomitantAgent.usingPerformedProcedure
false
bridg:ConcomitantAgent.usingPerformedProcedure
PerformedProcedure
bridg:ConcomitantAgent.usingPerformedProcedure
urn:CTRv1.0:ConcomitantAgent.using
bridg:PerformedProcedure.usedConcomitantAgent
use
bridg:PerformedProcedure.usedConcomitantAgent
none
bridg:PerformedProcedure.usedConcomitantAgent
usedConcomitantAgent
bridg:CooperativeGroup.credentialingOrganization
is credentialed by
bridg:CooperativeGroup.credentialingOrganization
none
bridg:CooperativeGroup.credentialingOrganization
credentialingOrganization
bridg:CooperativeGroup.credentialingOrganization
false
bridg:CooperativeGroup.credentialingOrganization
bridg:Organization.credentialedCooperativeGroup
credential
bridg:Organization.credentialedCooperativeGroup
none
bridg:Organization.credentialedCooperativeGroup
credentialedCooperativeGroup
bridg:CooperativeGroup.performingOrganization
is a function performed by
bridg:CooperativeGroup.performingOrganization
none
bridg:CooperativeGroup.performingOrganization
performingOrganization
bridg:CooperativeGroup.performingOrganization
false
bridg:CooperativeGroup.performingOrganization
bridg:Organization.performedCooperativeGroup
function as
bridg:Organization.performedCooperativeGroup
none
bridg:Organization.performedCooperativeGroup
performedCooperativeGroup
bridg:CooperativeGroupMember.groupingCooperativeGroup
is a member of
bridg:CooperativeGroupMember.groupingCooperativeGroup
none
bridg:CooperativeGroupMember.groupingCooperativeGroup
groupingCooperativeGroup
bridg:CooperativeGroupMember.groupingCooperativeGroup
false
bridg:CooperativeGroupMember.groupingCooperativeGroup
bridg:CooperativeGroup.groupedCooperativeGroupMember
have as a member
bridg:CooperativeGroup.groupedCooperativeGroupMember
none
bridg:CooperativeGroup.groupedCooperativeGroupMember
groupedCooperativeGroupMember
bridg:CooperativeGroupMember.performingOrganization
is a function performed by
bridg:CooperativeGroupMember.performingOrganization
none
bridg:CooperativeGroupMember.performingOrganization
performingOrganization
bridg:CooperativeGroupMember.performingOrganization
false
bridg:CooperativeGroupMember.performingOrganization
bridg:Organization.performedCooperativeGroupMember
function as
bridg:Organization.performedCooperativeGroupMember
none
bridg:Organization.performedCooperativeGroupMember
performedCooperativeGroupMember
bridg:DataMonitoringCommitteeCharterVersion.governedOversightCommittee
governs
bridg:DataMonitoringCommitteeCharterVersion.governedOversightCommittee
none
bridg:DataMonitoringCommitteeCharterVersion.governedOversightCommittee
governedOversightCommittee
bridg:DataMonitoringCommitteeCharterVersion.governedOversightCommittee
false
bridg:DataMonitoringCommitteeCharterVersion.governedOversightCommittee
bridg:OversightCommittee.governingDataMonitoringCommitteeCharterVersion
be governed by
bridg:OversightCommittee.governingDataMonitoringCommitteeCharterVersion
none
bridg:OversightCommittee.governingDataMonitoringCommitteeCharterVersion
governingDataMonitoringCommitteeCharterVersion
bridg:DataMonitoringCommitteeCharterVersion.influencedStatisticalAnalysisPlanVersion
influence
bridg:DataMonitoringCommitteeCharterVersion.influencedStatisticalAnalysisPlanVersion
none
bridg:DataMonitoringCommitteeCharterVersion.influencedStatisticalAnalysisPlanVersion
influencedStatisticalAnalysisPlanVersion
bridg:DataMonitoringCommitteeCharterVersion.influencedStatisticalAnalysisPlanVersion
false
bridg:DataMonitoringCommitteeCharterVersion.influencedStatisticalAnalysisPlanVersion
StatisticalAnalysisPlanVersion
bridg:DataMonitoringCommitteeCharterVersion.influencedStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:DataMonitoringCommitteeCharter.
bridg:StatisticalAnalysisPlanVersion.influencingDataMonitoringCommitteeCharterVersion
be influenced by
bridg:StatisticalAnalysisPlanVersion.influencingDataMonitoringCommitteeCharterVersion
none
bridg:StatisticalAnalysisPlanVersion.influencingDataMonitoringCommitteeCharterVersion
influencingDataMonitoringCommitteeCharterVersion
bridg:DefinedCompositionRelationship.componentDefinedActivity
is the parent of
bridg:DefinedCompositionRelationship.componentDefinedActivity
none
bridg:DefinedCompositionRelationship.componentDefinedActivity
componentDefinedActivity
bridg:DefinedCompositionRelationship.componentDefinedActivity
false
bridg:DefinedCompositionRelationship.componentDefinedActivity
DefinedActivity
bridg:DefinedCompositionRelationship.componentDefinedActivity
urn:CTRv1.0:DefinedCompositionRelationship.component
bridg:DefinedActivity.compositeDefinedCompositionRelationship
be the component of
bridg:DefinedActivity.compositeDefinedCompositionRelationship
none
bridg:DefinedActivity.compositeDefinedCompositionRelationship
compositeDefinedCompositionRelationship
bridg:DefinedCompositionRelationship.compositeDefinedActivity
is the component of
bridg:DefinedCompositionRelationship.compositeDefinedActivity
none
bridg:DefinedCompositionRelationship.compositeDefinedActivity
compositeDefinedActivity
bridg:DefinedCompositionRelationship.compositeDefinedActivity
false
bridg:DefinedCompositionRelationship.compositeDefinedActivity
DefinedActivity
bridg:DefinedCompositionRelationship.compositeDefinedActivity
urn:CTRv1.0:DefinedCompositionRelationship.composite
bridg:DefinedActivity.componentDefinedCompositionRelationship
be the parent of
bridg:DefinedActivity.componentDefinedCompositionRelationship
none
bridg:DefinedActivity.componentDefinedCompositionRelationship
componentDefinedCompositionRelationship
bridg:DefinedContingentOnRelationship.contingentDefinedActivity
is a condition for
bridg:DefinedContingentOnRelationship.contingentDefinedActivity
none
bridg:DefinedContingentOnRelationship.contingentDefinedActivity
contingentDefinedActivity
bridg:DefinedContingentOnRelationship.contingentDefinedActivity
false
bridg:DefinedContingentOnRelationship.contingentDefinedActivity
DefinedActivity
bridg:DefinedContingentOnRelationship.contingentDefinedActivity
urn:CTRv1.0:DefinedContingentOnRelationship.contingent
bridg:DefinedActivity.prerequisiteDefinedContingentOnRelationship
be contingent upon
bridg:DefinedActivity.prerequisiteDefinedContingentOnRelationship
none
bridg:DefinedActivity.prerequisiteDefinedContingentOnRelationship
prerequisiteDefinedContingentOnRelationship
bridg:DefinedContingentOnRelationship.prerequisiteDefinedActivity
be contingent upon
bridg:DefinedContingentOnRelationship.prerequisiteDefinedActivity
none
bridg:DefinedContingentOnRelationship.prerequisiteDefinedActivity
prerequisiteDefinedActivity
bridg:DefinedContingentOnRelationship.prerequisiteDefinedActivity
false
bridg:DefinedContingentOnRelationship.prerequisiteDefinedActivity
DefinedActivity
bridg:DefinedContingentOnRelationship.prerequisiteDefinedActivity
urn:CTRv1.0:DefinedContingentOnRelationship.prerequisite
bridg:DefinedActivity.contingentDefinedContingentOnRelationship
be a condition for
bridg:DefinedActivity.contingentDefinedContingentOnRelationship
none
bridg:DefinedActivity.contingentDefinedContingentOnRelationship
contingentDefinedContingentOnRelationship
bridg:DefinedContingentOnRelationship.prerequisiteDefinedCriterionGroup
be contingent upon
bridg:DefinedContingentOnRelationship.prerequisiteDefinedCriterionGroup
none
bridg:DefinedContingentOnRelationship.prerequisiteDefinedCriterionGroup
prerequisiteDefinedCriterionGroup
bridg:DefinedContingentOnRelationship.prerequisiteDefinedCriterionGroup
false
bridg:DefinedContingentOnRelationship.prerequisiteDefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedContingentOnRelationship.prerequisiteDefinedCriterionGroup
urn:CTRv1.0:DefinedContingentOnRelationship.prerequisite
bridg:DefinedCriterionGroup.contingentDefinedContingentOnRelationship
be a condition for
bridg:DefinedCriterionGroup.contingentDefinedContingentOnRelationship
none
bridg:DefinedCriterionGroup.contingentDefinedContingentOnRelationship
contingentDefinedContingentOnRelationship
bridg:DefinedContingentOnRelationship.prerequisiteDefinedObservationResult
be contingent upon
bridg:DefinedContingentOnRelationship.prerequisiteDefinedObservationResult
none
bridg:DefinedContingentOnRelationship.prerequisiteDefinedObservationResult
prerequisiteDefinedObservationResult
bridg:DefinedContingentOnRelationship.prerequisiteDefinedObservationResult
false
bridg:DefinedContingentOnRelationship.prerequisiteDefinedObservationResult
DefinedObservationResult
bridg:DefinedContingentOnRelationship.prerequisiteDefinedObservationResult
urn:CTRv1.0:DefinedContingentOnRelationship.prerequisite
bridg:DefinedObservationResult.contingentDefinedContingentOnRelationship
be a condition for
bridg:DefinedObservationResult.contingentDefinedContingentOnRelationship
none
bridg:DefinedObservationResult.contingentDefinedContingentOnRelationship
contingentDefinedContingentOnRelationship
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedActivity
be the parent of
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedActivity
none
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedActivity
componentDefinedActivity
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedActivity
false
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedActivity
DefinedActivity
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedActivity
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship.component
bridg:DefinedActivity.compositeDefinedCriterionGroupCompositionRelationship
be the component of
bridg:DefinedActivity.compositeDefinedCriterionGroupCompositionRelationship
none
bridg:DefinedActivity.compositeDefinedCriterionGroupCompositionRelationship
compositeDefinedCriterionGroupCompositionRelationship
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedCriterionGroup
be the parent of
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedCriterionGroup
none
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedCriterionGroup
componentDefinedCriterionGroup
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedCriterionGroup
false
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedCriterionGroup
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship.component
bridg:DefinedCriterionGroup.compositeDefinedCriterionGroupCompositionRelationship
be the component of
bridg:DefinedCriterionGroup.compositeDefinedCriterionGroupCompositionRelationship
none
bridg:DefinedCriterionGroup.compositeDefinedCriterionGroupCompositionRelationship
compositeDefinedCriterionGroupCompositionRelationship
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedObservationResult
be the parent of
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedObservationResult
none
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedObservationResult
componentDefinedObservationResult
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedObservationResult
false
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedObservationResult
DefinedObservationResult
bridg:DefinedCriterionGroupCompositionRelationship.componentDefinedObservationResult
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship.component
bridg:DefinedObservationResult.compositeDefinedCriterionGroupCompositionRelationship
be the component of
bridg:DefinedObservationResult.compositeDefinedCriterionGroupCompositionRelationship
none
bridg:DefinedObservationResult.compositeDefinedCriterionGroupCompositionRelationship
compositeDefinedCriterionGroupCompositionRelationship
bridg:DefinedCriterionGroupCompositionRelationship.compositeDefinedCriterionGroup
is the component of
bridg:DefinedCriterionGroupCompositionRelationship.compositeDefinedCriterionGroup
none
bridg:DefinedCriterionGroupCompositionRelationship.compositeDefinedCriterionGroup
compositeDefinedCriterionGroup
bridg:DefinedCriterionGroupCompositionRelationship.compositeDefinedCriterionGroup
false
bridg:DefinedCriterionGroupCompositionRelationship.compositeDefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedCriterionGroupCompositionRelationship.compositeDefinedCriterionGroup
urn:CTRv1.0:DefinedCriterionGroupCompositionRelationship.composite
bridg:DefinedCriterionGroup.componentDefinedCriterionGroupCompositionRelationship
be the parent of
bridg:DefinedCriterionGroup.componentDefinedCriterionGroupCompositionRelationship
none
bridg:DefinedCriterionGroup.componentDefinedCriterionGroupCompositionRelationship
componentDefinedCriterionGroupCompositionRelationship
bridg:DefinedCriterionGroupOptionRelationship.choiceDefinedCriterionGroup
is an option that can satisfy
bridg:DefinedCriterionGroupOptionRelationship.choiceDefinedCriterionGroup
none
bridg:DefinedCriterionGroupOptionRelationship.choiceDefinedCriterionGroup
choiceDefinedCriterionGroup
bridg:DefinedCriterionGroupOptionRelationship.choiceDefinedCriterionGroup
false
bridg:DefinedCriterionGroupOptionRelationship.choiceDefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedCriterionGroupOptionRelationship.choiceDefinedCriterionGroup
urn:CTRv1.0:DefinedCriterionGroupOptionRelationship.choice
bridg:DefinedCriterionGroup.optionDefinedCriterionGroupOptionRelationship
be a choice that has as option
bridg:DefinedCriterionGroup.optionDefinedCriterionGroupOptionRelationship
none
bridg:DefinedCriterionGroup.optionDefinedCriterionGroupOptionRelationship
optionDefinedCriterionGroupOptionRelationship
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedActivity
be a choice that has as option
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedActivity
none
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedActivity
optionDefinedActivity
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedActivity
false
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedActivity
DefinedActivity
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedActivity
urn:CTRv1.0:DefinedCriterionGroupOptionRelationship.option
bridg:DefinedActivity.choiceDefinedCriterionGroupOptionRelationship
be an option that can satisfy
bridg:DefinedActivity.choiceDefinedCriterionGroupOptionRelationship
none
bridg:DefinedActivity.choiceDefinedCriterionGroupOptionRelationship
choiceDefinedCriterionGroupOptionRelationship
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedCriterionGroup
be a choice that has as option
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedCriterionGroup
none
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedCriterionGroup
optionDefinedCriterionGroup
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedCriterionGroup
false
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedCriterionGroup
urn:CTRv1.0:DefinedCriterionGroupOptionRelationship.option
bridg:DefinedCriterionGroup.choiceDefinedCriterionGroupOptionRelationship
be an option that can satisfy
bridg:DefinedCriterionGroup.choiceDefinedCriterionGroupOptionRelationship
none
bridg:DefinedCriterionGroup.choiceDefinedCriterionGroupOptionRelationship
choiceDefinedCriterionGroupOptionRelationship
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedObservationResult
be a choice that has as option
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedObservationResult
none
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedObservationResult
optionDefinedObservationResult
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedObservationResult
false
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedObservationResult
DefinedObservationResult
bridg:DefinedCriterionGroupOptionRelationship.optionDefinedObservationResult
urn:CTRv1.0:DefinedCriterionGroupOptionRelationship.option
bridg:DefinedObservationResult.choiceDefinedCriterionGroupOptionRelationship
be an option that can satisfy
bridg:DefinedObservationResult.choiceDefinedCriterionGroupOptionRelationship
none
bridg:DefinedObservationResult.choiceDefinedCriterionGroupOptionRelationship
choiceDefinedCriterionGroupOptionRelationship
bridg:DefinedExpressionVariableRelationship.referencedDefinedObservation
is a reference to
bridg:DefinedExpressionVariableRelationship.referencedDefinedObservation
none
bridg:DefinedExpressionVariableRelationship.referencedDefinedObservation
referencedDefinedObservation
bridg:DefinedExpressionVariableRelationship.referencedDefinedObservation
false
bridg:DefinedExpressionVariableRelationship.referencedDefinedObservation
DefinedObservation
bridg:DefinedExpressionVariableRelationship.referencedDefinedObservation
urn:CTRv1.0:DefinedExpressionVariableRelationship.referenced
bridg:DefinedObservation.referencingDefinedExpressionVariableRelationship
be referenced by
bridg:DefinedObservation.referencingDefinedExpressionVariableRelationship
none
bridg:DefinedObservation.referencingDefinedExpressionVariableRelationship
referencingDefinedExpressionVariableRelationship
bridg:DefinedExpressionVariableRelationship.usingDefinedSubstanceAdministration
is used in
bridg:DefinedExpressionVariableRelationship.usingDefinedSubstanceAdministration
none
bridg:DefinedExpressionVariableRelationship.usingDefinedSubstanceAdministration
usingDefinedSubstanceAdministration
bridg:DefinedExpressionVariableRelationship.usingDefinedSubstanceAdministration
false
bridg:DefinedExpressionVariableRelationship.usingDefinedSubstanceAdministration
DefinedSubstanceAdministration
bridg:DefinedExpressionVariableRelationship.usingDefinedSubstanceAdministration
urn:CTRv1.0:DefinedExpressionVariableRelationship.using
bridg:DefinedSubstanceAdministration.usedDefinedExpressionVariableRelationship
use
bridg:DefinedSubstanceAdministration.usedDefinedExpressionVariableRelationship
none
bridg:DefinedSubstanceAdministration.usedDefinedExpressionVariableRelationship
usedDefinedExpressionVariableRelationship
bridg:DefinedMaterialStorage.storedSpecimen
stores
bridg:DefinedMaterialStorage.storedSpecimen
none
bridg:DefinedMaterialStorage.storedSpecimen
storedSpecimen
bridg:DefinedMaterialStorage.storedSpecimen
false
bridg:DefinedMaterialStorage.storedSpecimen
bridg:Specimen.storingDefinedSpecimenStorage
be stored during
bridg:Specimen.storingDefinedSpecimenStorage
none
bridg:Specimen.storingDefinedSpecimenStorage
storingDefinedSpecimenStorage
bridg:DefinedNotification.attachedDocumentVersion
have as an attachment
bridg:DefinedNotification.attachedDocumentVersion
none
bridg:DefinedNotification.attachedDocumentVersion
attachedDocumentVersion
bridg:DefinedNotification.attachedDocumentVersion
false
bridg:DefinedNotification.attachedDocumentVersion
bridg:DocumentVersion.attachingDefinedNotification
be an attachment on
bridg:DocumentVersion.attachingDefinedNotification
none
bridg:DocumentVersion.attachingDefinedNotification
attachingDefinedNotification
bridg:DefinedObservation.focusingDefinedActivity
have as focal context
bridg:DefinedObservation.focusingDefinedActivity
none
bridg:DefinedObservation.focusingDefinedActivity
focusingDefinedActivity
bridg:DefinedObservation.focusingDefinedActivity
false
bridg:DefinedObservation.focusingDefinedActivity
bridg:DefinedActivity.focusedDefinedObservation
be the focal context for
bridg:DefinedActivity.focusedDefinedObservation
none
bridg:DefinedActivity.focusedDefinedObservation
focusedDefinedObservation
bridg:DefinedObservation.focusingDefinedCriterionGroup
have as focal context
bridg:DefinedObservation.focusingDefinedCriterionGroup
none
bridg:DefinedObservation.focusingDefinedCriterionGroup
focusingDefinedCriterionGroup
bridg:DefinedObservation.focusingDefinedCriterionGroup
false
bridg:DefinedObservation.focusingDefinedCriterionGroup
bridg:DefinedObservation.focusingDefinedCriterionGroup
Was there a liver chemistry event for the lab samples collected at this visit?
bridg:DefinedObservation.focusingDefinedCriterionGroup
DEFINITION:
EXAMPLE(S):
OTHER NAME(S):
NOTE(S):
bridg:DefinedCriterionGroup.focusedDefinedObservation
be the focal context for
bridg:DefinedCriterionGroup.focusedDefinedObservation
none
bridg:DefinedCriterionGroup.focusedDefinedObservation
focusedDefinedObservation
bridg:DefinedObservation.focusingDefinedObservationResult
have as focal context
bridg:DefinedObservation.focusingDefinedObservationResult
none
bridg:DefinedObservation.focusingDefinedObservationResult
focusingDefinedObservationResult
bridg:DefinedObservation.focusingDefinedObservationResult
false
bridg:DefinedObservation.focusingDefinedObservationResult
DefinedObservationResult
bridg:DefinedObservation.focusingDefinedObservationResult
urn:CTRv1.0:DefinedObservation.focusing
bridg:DefinedObservationResult.focusedDefinedObservation
be the focal context for
bridg:DefinedObservationResult.focusedDefinedObservation
none
bridg:DefinedObservationResult.focusedDefinedObservation
focusedDefinedObservation
bridg:DefinedObservationResult.producingDefinedObservation
is a result of
bridg:DefinedObservationResult.producingDefinedObservation
none
bridg:DefinedObservationResult.producingDefinedObservation
producingDefinedObservation
bridg:DefinedObservationResult.producingDefinedObservation
false
bridg:DefinedObservationResult.producingDefinedObservation
DefinedObservation
bridg:DefinedObservationResult.producingDefinedObservation
urn:CTRRr3:DefinedObservationResult.producing
DefinedObservation
bridg:DefinedObservationResult.producingDefinedObservation
urn:CTRv1.0:DefinedObservationResult.producing
bridg:DefinedObservation.producedDefinedObservationResult
result in
bridg:DefinedObservation.producedDefinedObservationResult
none
bridg:DefinedObservation.producedDefinedObservationResult
producedDefinedObservationResult
bridg:DefinedOptionRelationship.choiceDefinedActivity
is an option that can satisfy
bridg:DefinedOptionRelationship.choiceDefinedActivity
none
bridg:DefinedOptionRelationship.choiceDefinedActivity
choiceDefinedActivity
bridg:DefinedOptionRelationship.choiceDefinedActivity
false
bridg:DefinedOptionRelationship.choiceDefinedActivity
DefinedActivity
bridg:DefinedOptionRelationship.choiceDefinedActivity
urn:CTRv1.0:DefinedOptionRelationship.choice
bridg:DefinedActivity.optionDefinedOptionRelationship
be a choice that has as option
bridg:DefinedActivity.optionDefinedOptionRelationship
none
bridg:DefinedActivity.optionDefinedOptionRelationship
optionDefinedOptionRelationship
bridg:DefinedOptionRelationship.optionDefinedActivity
is a choice that has as option
bridg:DefinedOptionRelationship.optionDefinedActivity
none
bridg:DefinedOptionRelationship.optionDefinedActivity
optionDefinedActivity
bridg:DefinedOptionRelationship.optionDefinedActivity
false
bridg:DefinedOptionRelationship.optionDefinedActivity
DefinedActivity
bridg:DefinedOptionRelationship.optionDefinedActivity
urn:CTRv1.0:DefinedOptionRelationship.option
bridg:DefinedActivity.choiceDefinedOptionRelationship
be an option that can satisfy
bridg:DefinedActivity.choiceDefinedOptionRelationship
none
bridg:DefinedActivity.choiceDefinedOptionRelationship
choiceDefinedOptionRelationship
bridg:DefinedProcedure.usedProduct
use
bridg:DefinedProcedure.usedProduct
none
bridg:DefinedProcedure.usedProduct
usedProduct
bridg:DefinedProcedure.usedProduct
false
bridg:DefinedProcedure.usedProduct
Product
bridg:DefinedProcedure.usedProduct
urn:CTRRr3:DefinedProcedure.used
Product
bridg:DefinedProcedure.usedProduct
urn:CTRv1.0:DefinedProcedure.used
bridg:Product.usingDefinedProcedure
be used during
bridg:Product.usingDefinedProcedure
none
bridg:Product.usingDefinedProcedure
usingDefinedProcedure
bridg:DefinedRepeatActivityUntilRule.repeatedDefinedActivity
triggers the cessation of
bridg:DefinedRepeatActivityUntilRule.repeatedDefinedActivity
none
bridg:DefinedRepeatActivityUntilRule.repeatedDefinedActivity
repeatedDefinedActivity
bridg:DefinedRepeatActivityUntilRule.repeatedDefinedActivity
false
bridg:DefinedRepeatActivityUntilRule.repeatedDefinedActivity
DefinedActivity
bridg:DefinedRepeatActivityUntilRule.repeatedDefinedActivity
urn:CTRv1.0:DefinedRepeatActivityUntilRule.repeated
bridg:DefinedActivity.triggeringDefinedRepeatActivityUntilRule
be repeated until
bridg:DefinedActivity.triggeringDefinedRepeatActivityUntilRule
none
bridg:DefinedActivity.triggeringDefinedRepeatActivityUntilRule
triggeringDefinedRepeatActivityUntilRule
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedActivity
be repeated until
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedActivity
none
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedActivity
triggeringDefinedActivity
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedActivity
false
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedActivity
DefinedActivity
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedActivity
urn:CTRv1.0:DefinedRepeatActivityUntilRule.triggering
bridg:DefinedActivity.repeatedDefinedRepeatActivityUntilRule
trigger the cessation of
bridg:DefinedActivity.repeatedDefinedRepeatActivityUntilRule
none
bridg:DefinedActivity.repeatedDefinedRepeatActivityUntilRule
repeatedDefinedRepeatActivityUntilRule
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedCriterionGroup
be repeated until
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedCriterionGroup
none
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedCriterionGroup
triggeringDefinedCriterionGroup
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedCriterionGroup
false
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedCriterionGroup
DefinedCriterionGroup
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedCriterionGroup
urn:CTRv1.0:DefinedRepeatActivityUntilRule.triggering
bridg:DefinedCriterionGroup.repeatedDefinedRepeatActivityUntilRule
trigger the cessation of
bridg:DefinedCriterionGroup.repeatedDefinedRepeatActivityUntilRule
none
bridg:DefinedCriterionGroup.repeatedDefinedRepeatActivityUntilRule
repeatedDefinedRepeatActivityUntilRule
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedObservationResult
be repeated until
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedObservationResult
none
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedObservationResult
triggeringDefinedObservationResult
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedObservationResult
false
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedObservationResult
DefinedObservationResult
bridg:DefinedRepeatActivityUntilRule.triggeringDefinedObservationResult
urn:CTRv1.0:DefinedRepeatActivityUntilRule.triggering
bridg:DefinedObservationResult.repeatedDefinedRepeatActivityUntilRule
trigger the cessation of
bridg:DefinedObservationResult.repeatedDefinedRepeatActivityUntilRule
none
bridg:DefinedObservationResult.repeatedDefinedRepeatActivityUntilRule
repeatedDefinedRepeatActivityUntilRule
bridg:DefinedSpecimenCollection.producedSpecimen
results in
bridg:DefinedSpecimenCollection.producedSpecimen
none
bridg:DefinedSpecimenCollection.producedSpecimen
producedSpecimen
bridg:DefinedSpecimenCollection.producedSpecimen
false
bridg:DefinedSpecimenCollection.producedSpecimen
Specimen
bridg:DefinedSpecimenCollection.producedSpecimen
urn:CTRv1.0:DefinedSpecimenCollection.produced
bridg:Specimen.producingDefinedSpecimenCollection
be a result of
bridg:Specimen.producingDefinedSpecimenCollection
none
bridg:Specimen.producingDefinedSpecimenCollection
producingDefinedSpecimenCollection
bridg:DefinedStudyAgentTransfer.transferredProduct
is a transfer of
bridg:DefinedStudyAgentTransfer.transferredProduct
none
bridg:DefinedStudyAgentTransfer.transferredProduct
transferredProduct
bridg:DefinedStudyAgentTransfer.transferredProduct
false
bridg:DefinedStudyAgentTransfer.transferredProduct
bridg:Product.transferringDefinedStudyAgentTransfer
be transferred during
bridg:Product.transferringDefinedStudyAgentTransfer
none
bridg:Product.transferringDefinedStudyAgentTransfer
transferringDefinedStudyAgentTransfer
bridg:DefinedStudySubjectMilestone.usedDocumentVersion
use
bridg:DefinedStudySubjectMilestone.usedDocumentVersion
none
bridg:DefinedStudySubjectMilestone.usedDocumentVersion
usedDocumentVersion
bridg:DefinedStudySubjectMilestone.usedDocumentVersion
false
bridg:DefinedStudySubjectMilestone.usedDocumentVersion
DocumentVersion
bridg:DefinedStudySubjectMilestone.usedDocumentVersion
urn:CTRv1.0:DefinedStudySubjectMilestone.used
bridg:DocumentVersion.usingDefinedStudySubjectMilestone
be used for
bridg:DocumentVersion.usingDefinedStudySubjectMilestone
none
bridg:DocumentVersion.usingDefinedStudySubjectMilestone
usingDefinedStudySubjectMilestone
bridg:Distributor.performingOrganization
is a function performed by
bridg:Distributor.performingOrganization
none
bridg:Distributor.performingOrganization
performingOrganization
bridg:Distributor.performingOrganization
false
bridg:Distributor.performingOrganization
bridg:Organization.performedDistributor
function as
bridg:Organization.performedDistributor
none
bridg:Organization.performedDistributor
performedDistributor
bridg:Distributor.providingProduct
provides
bridg:Distributor.providingProduct
none
bridg:Distributor.providingProduct
providingProduct
bridg:Distributor.providingProduct
false
bridg:Distributor.providingProduct
bridg:Product.providedDistributor
be provided by
bridg:Product.providedDistributor
none
bridg:Product.providedDistributor
providedDistributor
bridg:Distributor.representedProcessor
functions as an outlet for
bridg:Distributor.representedProcessor
none
bridg:Distributor.representedProcessor
representedProcessor
bridg:Distributor.representedProcessor
false
bridg:Distributor.representedProcessor
bridg:Processor.representingDistributor
have as an outlet
bridg:Processor.representingDistributor
none
bridg:Processor.representingDistributor
representingDistributor
bridg:DocumentAuthor.authoredDocumentVersion
authors
bridg:DocumentAuthor.authoredDocumentVersion
none
bridg:DocumentAuthor.authoredDocumentVersion
authoredDocumentVersion
bridg:DocumentAuthor.authoredDocumentVersion
false
bridg:DocumentAuthor.authoredDocumentVersion
DocumentVersion
bridg:DocumentAuthor.authoredDocumentVersion
urn:CTRv1.0:DocumentAuthor.authored
bridg:DocumentVersion.authoringDocumentAuthor
is authored by
bridg:DocumentVersion.authoringDocumentAuthor
none
bridg:DocumentVersion.authoringDocumentAuthor
authoringDocumentAuthor
bridg:DocumentAuthor.performingAssociatedBiologicEntity
be a function performed by
bridg:DocumentAuthor.performingAssociatedBiologicEntity
none
bridg:DocumentAuthor.performingAssociatedBiologicEntity
performingAssociatedBiologicEntity
bridg:DocumentAuthor.performingAssociatedBiologicEntity
false
bridg:DocumentAuthor.performingAssociatedBiologicEntity
AssociatedBiologicEntity
bridg:DocumentAuthor.performingAssociatedBiologicEntity
urn:CTRv1.0:DocumentAuthor.performing
bridg:AssociatedBiologicEntity.performedDocumentAuthor
function as
bridg:AssociatedBiologicEntity.performedDocumentAuthor
none
bridg:AssociatedBiologicEntity.performedDocumentAuthor
performedDocumentAuthor
bridg:DocumentAuthor.performingHealthcareProvider
be a function performed by
bridg:DocumentAuthor.performingHealthcareProvider
none
bridg:DocumentAuthor.performingHealthcareProvider
performingHealthcareProvider
bridg:DocumentAuthor.performingHealthcareProvider
false
bridg:DocumentAuthor.performingHealthcareProvider
HealthcareProvider
bridg:DocumentAuthor.performingHealthcareProvider
urn:CTRv1.0:DocumentAuthor.performing
bridg:HealthcareProvider.performedDocumentAuthor
function as
bridg:HealthcareProvider.performedDocumentAuthor
none
bridg:HealthcareProvider.performedDocumentAuthor
performedDocumentAuthor
bridg:DocumentAuthor.performingResearchStaff
be a function performed by
bridg:DocumentAuthor.performingResearchStaff
none
bridg:DocumentAuthor.performingResearchStaff
performingResearchStaff
bridg:DocumentAuthor.performingResearchStaff
false
bridg:DocumentAuthor.performingResearchStaff
ResearchStaff
bridg:DocumentAuthor.performingResearchStaff
urn:CTRv1.0:DocumentAuthor.performing
bridg:ResearchStaff.performedDocumentAuthor
function as
bridg:ResearchStaff.performedDocumentAuthor
none
bridg:ResearchStaff.performedDocumentAuthor
performedDocumentAuthor
bridg:DocumentAuthor.performingSubject
be a function performed by
bridg:DocumentAuthor.performingSubject
none
bridg:DocumentAuthor.performingSubject
performingSubject
bridg:DocumentAuthor.performingSubject
false
bridg:DocumentAuthor.performingSubject
Subject
bridg:DocumentAuthor.performingSubject
urn:CTRv1.0:DocumentAuthor.performing
bridg:Subject.performedDocumentAuthor
function as
bridg:Subject.performedDocumentAuthor
none
bridg:Subject.performedDocumentAuthor
performedDocumentAuthor
bridg:DocumentIdentifier.assigningOrganization
be assigned by
bridg:DocumentIdentifier.assigningOrganization
none
bridg:DocumentIdentifier.assigningOrganization
assigningOrganization
bridg:DocumentIdentifier.assigningOrganization
false
bridg:DocumentIdentifier.assigningOrganization
Organization
bridg:DocumentIdentifier.assigningOrganization
urn:CTRRr3:DocumentIdentifier.issuing
Organization
bridg:DocumentIdentifier.assigningOrganization
urn:CTRv1.0:DocumentIdentifier.assigning
bridg:DocumentIdentifier.assigningOrganization
urn:Lab:Study.assigningAuthority
bridg:Organization.assignedDocumentIdentifier
assign
bridg:Organization.assignedDocumentIdentifier
none
bridg:Organization.assignedDocumentIdentifier
assignedDocumentIdentifier
bridg:DocumentIdentifier.assigningStudyRegistry
be assigned by
bridg:DocumentIdentifier.assigningStudyRegistry
none
bridg:DocumentIdentifier.assigningStudyRegistry
assigningStudyRegistry
bridg:DocumentIdentifier.assigningStudyRegistry
false
bridg:DocumentIdentifier.assigningStudyRegistry
StudyRegistry
bridg:DocumentIdentifier.assigningStudyRegistry
urn:CTRRr3:DocumentIdentifier.issuing
StudyRegistry
bridg:DocumentIdentifier.assigningStudyRegistry
urn:CTRv1.0:DocumentIdentifier.assigning
bridg:StudyRegistry.assignedDocumentIdentifier
assign
bridg:StudyRegistry.assignedDocumentIdentifier
none
bridg:StudyRegistry.assignedDocumentIdentifier
assignedDocumentIdentifier
bridg:DocumentIdentifier.assigningSystemOfRecord
be assigned by
bridg:DocumentIdentifier.assigningSystemOfRecord
none
bridg:DocumentIdentifier.assigningSystemOfRecord
assigningSystemOfRecord
bridg:DocumentIdentifier.assigningSystemOfRecord
false
bridg:DocumentIdentifier.assigningSystemOfRecord
SystemOfRecord
bridg:DocumentIdentifier.assigningSystemOfRecord
urn:CTRv1.0:DocumentIdentifier.assigning
bridg:SystemOfRecord.assignedDocumentIdentifier
assign
bridg:SystemOfRecord.assignedDocumentIdentifier
none
bridg:SystemOfRecord.assignedDocumentIdentifier
assignedDocumentIdentifier
bridg:DocumentIdentifier.identifiedDocument
identifies
bridg:DocumentIdentifier.identifiedDocument
none
bridg:DocumentIdentifier.identifiedDocument
identifiedDocument
bridg:DocumentIdentifier.identifiedDocument
false
bridg:DocumentIdentifier.identifiedDocument
bridg:DocumentIdentifier.identifiedDocument
urn:C3PR:StudyProtocol.identifier
Document
bridg:DocumentIdentifier.identifiedDocument
urn:CTRRr3:DocumentIdentifier.identified
Document
bridg:DocumentIdentifier.identifiedDocument
urn:CTRv1.0:DocumentIdentifier.identified
Document
bridg:DocumentIdentifier.identifiedDocument
urn:Statistics_v1.0:DocumentIdentifier.identifiedDocument
bridg:Document.identifyingDocumentIdentifier
be identified by
bridg:Document.identifyingDocumentIdentifier
none
bridg:Document.identifyingDocumentIdentifier
identifyingDocumentIdentifier
bridg:DocumentIdentifier.resulted_inPerformedStudyAdministrativeActivity
be assigned during
bridg:DocumentIdentifier.resulted_inPerformedStudyAdministrativeActivity
none
bridg:DocumentIdentifier.resulted_inPerformedStudyAdministrativeActivity
resulted inPerformedStudyAdministrativeActivity
bridg:DocumentIdentifier.resulted_inPerformedStudyAdministrativeActivity
false
bridg:DocumentIdentifier.resulted_inPerformedStudyAdministrativeActivity
PerformedStudyAdministrativeActivity
bridg:DocumentIdentifier.resulted_inPerformedStudyAdministrativeActivity
urn:CTRv1.0:DocumentIdentifier.resulted_in
bridg:PerformedStudyAdministrativeActivity.assignedDocumentIdentifier
result in
bridg:PerformedStudyAdministrativeActivity.assignedDocumentIdentifier
none
bridg:PerformedStudyAdministrativeActivity.assignedDocumentIdentifier
assignedDocumentIdentifier
bridg:DocumentVersion.versionedDocument
is a version of
bridg:DocumentVersion.versionedDocument
none
bridg:DocumentVersion.versionedDocument
versionedDocument
bridg:DocumentVersion.versionedDocument
false
bridg:DocumentVersion.versionedDocument
Document
bridg:DocumentVersion.versionedDocument
urn:CTRv1.0:DocumentVersion.versioned
Document
bridg:DocumentVersion.versionedDocument
urn:Statistics_v1.0:DocumentVersion.versionedDocument
bridg:Document.versioningDocumentVersion
have as a version
bridg:Document.versioningDocumentVersion
none
bridg:Document.versioningDocumentVersion
versioningDocumentVersion
bridg:DocumentVersionRelationship.sourceDocumentVersion
has as source
bridg:DocumentVersionRelationship.sourceDocumentVersion
none
bridg:DocumentVersionRelationship.sourceDocumentVersion
sourceDocumentVersion
bridg:DocumentVersionRelationship.sourceDocumentVersion
false
bridg:DocumentVersionRelationship.sourceDocumentVersion
DocumentVersion
bridg:DocumentVersionRelationship.sourceDocumentVersion
urn:CTRv1.0:DocumentVersionRelationship.source
bridg:DocumentVersion.targetDocumentVersionRelationship
be the source for
bridg:DocumentVersion.targetDocumentVersionRelationship
none
bridg:DocumentVersion.targetDocumentVersionRelationship
targetDocumentVersionRelationship
bridg:DocumentVersionRelationship.targetDocumentVersion
has as target
bridg:DocumentVersionRelationship.targetDocumentVersion
none
bridg:DocumentVersionRelationship.targetDocumentVersion
targetDocumentVersion
bridg:DocumentVersionRelationship.targetDocumentVersion
false
bridg:DocumentVersionRelationship.targetDocumentVersion
DocumentVersion
bridg:DocumentVersionRelationship.targetDocumentVersion
urn:CTRv1.0:DocumentVersionRelationship.target
bridg:DocumentVersion.sourceDocumentVersionRelationship
be the target for
bridg:DocumentVersion.sourceDocumentVersionRelationship
none
bridg:DocumentVersion.sourceDocumentVersionRelationship
sourceDocumentVersionRelationship
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
describes
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
none
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
describedDocumentVersion
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
false
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
DocumentWorkflowStatus
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
urn:CTRPv3.8:StudyProtocol.workflowStatus
DocumentVersion
bridg:DocumentVersionWorkflowStatus.describedDocumentVersion
urn:CTRv1.0:DocumentVersionWorkflowStatus.described
bridg:DocumentVersion.describingDocumentVersionWorkflowStatus
be described by
bridg:DocumentVersion.describingDocumentVersionWorkflowStatus
none
bridg:DocumentVersion.describingDocumentVersionWorkflowStatus
describingDocumentVersionWorkflowStatus
bridg:DonorRegistry.managingOrganization
is managed by
bridg:DonorRegistry.managingOrganization
none
bridg:DonorRegistry.managingOrganization
managingOrganization
bridg:DonorRegistry.managingOrganization
false
bridg:DonorRegistry.managingOrganization
Indicates the organization that manages the registry.
bridg:Organization.managedDonorRegistry
manage
bridg:Organization.managedDonorRegistry
none
bridg:Organization.managedDonorRegistry
managedDonorRegistry
bridg:Epoch.subdividedStudyProtocolVersion
is a division of
bridg:Epoch.subdividedStudyProtocolVersion
none
bridg:Epoch.subdividedStudyProtocolVersion
subdividedStudyProtocolVersion
bridg:Epoch.subdividedStudyProtocolVersion
false
bridg:Epoch.subdividedStudyProtocolVersion
Epoch
bridg:Epoch.subdividedStudyProtocolVersion
urn:CTRPv3.8:StudyProtocol.
StudyProtocolVersion
bridg:Epoch.subdividedStudyProtocolVersion
urn:CTRv1.0:Epoch.subdivided
bridg:Epoch.subdividedStudyProtocolVersion
urn:FDA_HL7_SD_SD_DSTU2012:plannedStudy/component1.typeCode
bridg:StudyProtocolVersion.subdividingEpoch
be divided into
bridg:StudyProtocolVersion.subdividingEpoch
none
bridg:StudyProtocolVersion.subdividingEpoch
subdividingEpoch
bridg:EvaluatedActivityRelationship.evaluatedPerformedActivity
evaluates
bridg:EvaluatedActivityRelationship.evaluatedPerformedActivity
none
bridg:EvaluatedActivityRelationship.evaluatedPerformedActivity
evaluatedPerformedActivity
bridg:EvaluatedActivityRelationship.evaluatedPerformedActivity
false
bridg:EvaluatedActivityRelationship.evaluatedPerformedActivity
PerformedActivity
bridg:EvaluatedActivityRelationship.evaluatedPerformedActivity
urn:CTRv1.0:EvaluatedActivityRelationship.evaluated
bridg:PerformedActivity.evaluatingEvaluatedActivityRelationship
be evaluated by
bridg:PerformedActivity.evaluatingEvaluatedActivityRelationship
none
bridg:PerformedActivity.evaluatingEvaluatedActivityRelationship
evaluatingEvaluatedActivityRelationship
bridg:EvaluatedActivityRelationship.evaluatingCausalAssessment
is evaluated by
bridg:EvaluatedActivityRelationship.evaluatingCausalAssessment
none
bridg:EvaluatedActivityRelationship.evaluatingCausalAssessment
evaluatingCausalAssessment
bridg:EvaluatedActivityRelationship.evaluatingCausalAssessment
false
bridg:EvaluatedActivityRelationship.evaluatingCausalAssessment
CausalAssessment
bridg:EvaluatedActivityRelationship.evaluatingCausalAssessment
urn:CTRv1.0:EvaluatedActivityRelationship.evaluating
bridg:CausalAssessment.evaluatedEvaluatedActivityRelationship
evaluate
bridg:CausalAssessment.evaluatedEvaluatedActivityRelationship
none
bridg:CausalAssessment.evaluatedEvaluatedActivityRelationship
evaluatedEvaluatedActivityRelationship
bridg:EvaluatedResultRelationship.evaluatedPerformedObservationResult
evaluates
bridg:EvaluatedResultRelationship.evaluatedPerformedObservationResult
none
bridg:EvaluatedResultRelationship.evaluatedPerformedObservationResult
evaluatedPerformedObservationResult
bridg:EvaluatedResultRelationship.evaluatedPerformedObservationResult
false
bridg:EvaluatedResultRelationship.evaluatedPerformedObservationResult
PerformedObservationResult
bridg:EvaluatedResultRelationship.evaluatedPerformedObservationResult
urn:CTRv1.0:EvaluatedResultRelationship.evaluated
bridg:PerformedObservationResult.evaluatingEvaluatedResultRelationship
be evaluated by
bridg:PerformedObservationResult.evaluatingEvaluatedResultRelationship
none
bridg:PerformedObservationResult.evaluatingEvaluatedResultRelationship
evaluatingEvaluatedResultRelationship
bridg:EvaluatedResultRelationship.evaluatingCausalAssessment
is evaluated by
bridg:EvaluatedResultRelationship.evaluatingCausalAssessment
none
bridg:EvaluatedResultRelationship.evaluatingCausalAssessment
evaluatingCausalAssessment
bridg:EvaluatedResultRelationship.evaluatingCausalAssessment
false
bridg:EvaluatedResultRelationship.evaluatingCausalAssessment
CausalAssessment
bridg:EvaluatedResultRelationship.evaluatingCausalAssessment
urn:CTRv1.0:EvaluatedResultRelationship.evaluating
bridg:CausalAssessment.evaluatedEvaluatedResultRelationship
evaluate
bridg:CausalAssessment.evaluatedEvaluatedResultRelationship
none
bridg:CausalAssessment.evaluatedEvaluatedResultRelationship
evaluatedEvaluatedResultRelationship
bridg:ExperimentalUnit.performedArm
have performed
bridg:ExperimentalUnit.performedArm
none
bridg:ExperimentalUnit.performedArm
performedArm
bridg:ExperimentalUnit.performedArm
false
bridg:ExperimentalUnit.performedArm
Indicates that an ExperimentalUnit was, at the end of their participation in a study, assigned to a particular arm based on their actual path through the study.
bridg:ExperimentalUnit.performedArm
This is derivable if the set of performed activities the ExperimentalUnit participated in are available.
Arm
bridg:ExperimentalUnit.performedArm
urn:CTRv1.0:ExperimentalUnit.assigning
bridg:Arm.performingExperimentalUnit
have been performed by
bridg:Arm.performingExperimentalUnit
none
bridg:Arm.performingExperimentalUnit
performingExperimentalUnit
bridg:ExperimentalUnit.performingBiologicEntity
be a function performed by
bridg:ExperimentalUnit.performingBiologicEntity
none
bridg:ExperimentalUnit.performingBiologicEntity
performingBiologicEntity
bridg:ExperimentalUnit.performingBiologicEntity
false
bridg:ExperimentalUnit.performingBiologicEntity
BiologicEntity
bridg:ExperimentalUnit.performingBiologicEntity
urn:CTRRr3:ExperimentalUnit.performing
BiologicEntity
bridg:ExperimentalUnit.performingBiologicEntity
urn:CTRv1.0:ExperimentalUnit.performing
bridg:BiologicEntity.performedExperimentalUnit
function as
bridg:BiologicEntity.performedExperimentalUnit
none
bridg:BiologicEntity.performedExperimentalUnit
performedExperimentalUnit
bridg:ExperimentalUnit.performingBiologicEntityGroup
be a function performed by
bridg:ExperimentalUnit.performingBiologicEntityGroup
none
bridg:ExperimentalUnit.performingBiologicEntityGroup
performingBiologicEntityGroup
bridg:ExperimentalUnit.performingBiologicEntityGroup
false
bridg:ExperimentalUnit.performingBiologicEntityGroup
BiologicEntityGroup
bridg:ExperimentalUnit.performingBiologicEntityGroup
urn:CTRv1.0:ExperimentalUnit.performing
bridg:BiologicEntityGroup.performedExperimentalUnit
function as
bridg:BiologicEntityGroup.performedExperimentalUnit
none
bridg:BiologicEntityGroup.performedExperimentalUnit
performedExperimentalUnit
bridg:ExperimentalUnit.performingBiologicEntityPart
be a function performed by
bridg:ExperimentalUnit.performingBiologicEntityPart
none
bridg:ExperimentalUnit.performingBiologicEntityPart
performingBiologicEntityPart
bridg:ExperimentalUnit.performingBiologicEntityPart
false
bridg:ExperimentalUnit.performingBiologicEntityPart
BiologicEntityPart
bridg:ExperimentalUnit.performingBiologicEntityPart
urn:CTRRr3:ExperimentalUnit.performing
BiologicEntityPart
bridg:ExperimentalUnit.performingBiologicEntityPart
urn:CTRv1.0:ExperimentalUnit.performing
bridg:BiologicEntityPart.performedExperimentalUnit
function as
bridg:BiologicEntityPart.performedExperimentalUnit
none
bridg:BiologicEntityPart.performedExperimentalUnit
performedExperimentalUnit
bridg:ExperimentalUnit.performingProduct
be a function performed by
bridg:ExperimentalUnit.performingProduct
none
bridg:ExperimentalUnit.performingProduct
performingProduct
bridg:ExperimentalUnit.performingProduct
false
bridg:ExperimentalUnit.performingProduct
Product
bridg:ExperimentalUnit.performingProduct
urn:CTRRr3:ExperimentalUnit.performing
Product
bridg:ExperimentalUnit.performingProduct
urn:CTRv1.0:ExperimentalUnit.performing
bridg:Product.performedExperimentalUnit
function as
bridg:Product.performedExperimentalUnit
none
bridg:Product.performedExperimentalUnit
performedExperimentalUnit
bridg:ExperimentalUnit.performingProductGroup
be a function performed by
bridg:ExperimentalUnit.performingProductGroup
none
bridg:ExperimentalUnit.performingProductGroup
performingProductGroup
bridg:ExperimentalUnit.performingProductGroup
false
bridg:ExperimentalUnit.performingProductGroup
bridg:ProductGroup.performedExperimentalUnit
function as
bridg:ProductGroup.performedExperimentalUnit
none
bridg:ProductGroup.performedExperimentalUnit
performedExperimentalUnit
bridg:ExperimentalUnit.performingSpecimen
be a function performed by
bridg:ExperimentalUnit.performingSpecimen
none
bridg:ExperimentalUnit.performingSpecimen
performingSpecimen
bridg:ExperimentalUnit.performingSpecimen
false
bridg:ExperimentalUnit.performingSpecimen
BiologicSpecimen
bridg:ExperimentalUnit.performingSpecimen
urn:CTRRr3:ExperimentalUnit.performing
Specimen
bridg:ExperimentalUnit.performingSpecimen
urn:CTRv1.0:ExperimentalUnit.performing
bridg:Specimen.performedExperimentalUnit
function as
bridg:Specimen.performedExperimentalUnit
none
bridg:Specimen.performedExperimentalUnit
performedExperimentalUnit
bridg:GeneralStatisticalConsideration.containingStatisticalAnalysisPlanVersion
is part of
bridg:GeneralStatisticalConsideration.containingStatisticalAnalysisPlanVersion
none
bridg:GeneralStatisticalConsideration.containingStatisticalAnalysisPlanVersion
containingStatisticalAnalysisPlanVersion
bridg:GeneralStatisticalConsideration.containingStatisticalAnalysisPlanVersion
false
bridg:GeneralStatisticalConsideration.containingStatisticalAnalysisPlanVersion
Identifies the considerations that inform the detailed design of the analysis plan.
StatisticalAnalysisPlanVersion
bridg:GeneralStatisticalConsideration.containingStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:GeneralStatisticalConsideration.
bridg:StatisticalAnalysisPlanVersion.containedGeneralStatisticalConsideration
have
bridg:StatisticalAnalysisPlanVersion.containedGeneralStatisticalConsideration
composite
bridg:StatisticalAnalysisPlanVersion.containedGeneralStatisticalConsideration
containedGeneralStatisticalConsideration
bridg:HealthcareFacility.performingOrganization
is a function performed by
bridg:HealthcareFacility.performingOrganization
none
bridg:HealthcareFacility.performingOrganization
performingOrganization
bridg:HealthcareFacility.performingOrganization
false
bridg:HealthcareFacility.performingOrganization
Organization
bridg:HealthcareFacility.performingOrganization
urn:CTRv1.0:HealthcareFacility.performing
bridg:Organization.performedHealthcareFacility
function as
bridg:Organization.performedHealthcareFacility
none
bridg:Organization.performedHealthcareFacility
performedHealthcareFacility
bridg:HealthcareProvider.employingOrganization
belong to a department at
bridg:HealthcareProvider.employingOrganization
none
bridg:HealthcareProvider.employingOrganization
employingOrganization
bridg:HealthcareProvider.employingOrganization
false
bridg:HealthcareProvider.employingOrganization
Organization
bridg:HealthcareProvider.employingOrganization
urn:CTRv1.0:HealthcareProvider.employing
bridg:Organization.employedHealthcareProvider
be the department for
bridg:Organization.employedHealthcareProvider
none
bridg:Organization.employedHealthcareProvider
employedHealthcareProvider
bridg:HealthcareProvider.performingPerson
is a function performed by
bridg:HealthcareProvider.performingPerson
none
bridg:HealthcareProvider.performingPerson
performingPerson
bridg:HealthcareProvider.performingPerson
false
bridg:HealthcareProvider.performingPerson
Person
bridg:HealthcareProvider.performingPerson
urn:CTRv1.0:HealthcareProvider.performing
bridg:Person.performedHealthcareProvider
function as
bridg:Person.performedHealthcareProvider
none
bridg:Person.performedHealthcareProvider
performedHealthcareProvider
bridg:HealthcareProvider.staffedHealthcareFacility
staff
bridg:HealthcareProvider.staffedHealthcareFacility
none
bridg:HealthcareProvider.staffedHealthcareFacility
staffedHealthcareFacility
bridg:HealthcareProvider.staffedHealthcareFacility
false
bridg:HealthcareProvider.staffedHealthcareFacility
HealthcareFacility
bridg:HealthcareProvider.staffedHealthcareFacility
urn:CTRv1.0:HealthcareProvider.staffed
bridg:HealthcareFacility.staffingHealthcareProvider
be staffed by
bridg:HealthcareFacility.staffingHealthcareProvider
none
bridg:HealthcareFacility.staffingHealthcareProvider
staffingHealthcareProvider
bridg:HealthcareProviderGroup.performingOrganization
is a function performed by
bridg:HealthcareProviderGroup.performingOrganization
none
bridg:HealthcareProviderGroup.performingOrganization
performingOrganization
bridg:HealthcareProviderGroup.performingOrganization
false
bridg:HealthcareProviderGroup.performingOrganization
bridg:Organization.performedHealthcareProviderGroup
function as
bridg:Organization.performedHealthcareProviderGroup
none
bridg:Organization.performedHealthcareProviderGroup
performedHealthcareProviderGroup
bridg:HealthcareProviderGroup.usingHealthcareFacility
is used to group staff for
bridg:HealthcareProviderGroup.usingHealthcareFacility
none
bridg:HealthcareProviderGroup.usingHealthcareFacility
usingHealthcareFacility
bridg:HealthcareProviderGroup.usingHealthcareFacility
false
bridg:HealthcareProviderGroup.usingHealthcareFacility
bridg:HealthcareFacility.usedHealthcareProviderGroup
group staff into
bridg:HealthcareFacility.usedHealthcareProviderGroup
none
bridg:HealthcareFacility.usedHealthcareProviderGroup
usedHealthcareProviderGroup
bridg:HealthcareProviderGroupMember.groupingHealthcareProviderGroup
belongs to
bridg:HealthcareProviderGroupMember.groupingHealthcareProviderGroup
none
bridg:HealthcareProviderGroupMember.groupingHealthcareProviderGroup
groupingHealthcareProviderGroup
bridg:HealthcareProviderGroupMember.groupingHealthcareProviderGroup
false
bridg:HealthcareProviderGroupMember.groupingHealthcareProviderGroup
bridg:HealthcareProviderGroup.groupedHealthcareProviderGroupMember
contains
bridg:HealthcareProviderGroup.groupedHealthcareProviderGroupMember
none
bridg:HealthcareProviderGroup.groupedHealthcareProviderGroupMember
groupedHealthcareProviderGroupMember
bridg:HealthcareProviderGroupMember.performingHealthcareProvider
is a function performed by
bridg:HealthcareProviderGroupMember.performingHealthcareProvider
none
bridg:HealthcareProviderGroupMember.performingHealthcareProvider
performingHealthcareProvider
bridg:HealthcareProviderGroupMember.performingHealthcareProvider
false
bridg:HealthcareProviderGroupMember.performingHealthcareProvider
bridg:HealthcareProvider.performedHealthcareProviderGroupMember
function as
bridg:HealthcareProvider.performedHealthcareProviderGroupMember
none
bridg:HealthcareProvider.performedHealthcareProviderGroupMember
performedHealthcareProviderGroupMember
bridg:IntegratedStatisticalAnalysisPlan.integratedStudyProtocol
integrates data from
bridg:IntegratedStatisticalAnalysisPlan.integratedStudyProtocol
none
bridg:IntegratedStatisticalAnalysisPlan.integratedStudyProtocol
integratedStudyProtocol
bridg:IntegratedStatisticalAnalysisPlan.integratedStudyProtocol
false
bridg:IntegratedStatisticalAnalysisPlan.integratedStudyProtocol
Identifies the study protocols whose data is used in the integrated statistical analysis plan.
StudyProtocol
bridg:IntegratedStatisticalAnalysisPlan.integratedStudyProtocol
urn:Statistics_v1.0:IntegratedStatisticalAnalysisPlan.
bridg:StudyProtocol.integratingIntegratedStatisticalAnalysisPlan
have data integrated from
bridg:StudyProtocol.integratingIntegratedStatisticalAnalysisPlan
none
bridg:StudyProtocol.integratingIntegratedStatisticalAnalysisPlan
integratingIntegratedStatisticalAnalysisPlan
bridg:Laboratory.performingOrganization
be a function performed by
bridg:Laboratory.performingOrganization
none
bridg:Laboratory.performingOrganization
performingOrganization
bridg:Laboratory.performingOrganization
false
bridg:Laboratory.performingOrganization
Organization
bridg:Laboratory.performingOrganization
urn:CTRv1.0:Laboratory.performing
bridg:Organization.performedLaboratory
function as
bridg:Organization.performedLaboratory
none
bridg:Organization.performedLaboratory
performedLaboratory
bridg:Material.producingDefinedMaterialProcessStep
have been produced by
bridg:Material.producingDefinedMaterialProcessStep
none
bridg:Material.producingDefinedMaterialProcessStep
producingDefinedMaterialProcessStep
bridg:Material.producingDefinedMaterialProcessStep
false
bridg:Material.producingDefinedMaterialProcessStep
Indicates that material is produced by a process step.
bridg:Material.producingDefinedMaterialProcessStep
A blood product has anticoagulants added to it to preserve the product
bridg:Material.producingDefinedMaterialProcessStep
A blood product has growth factor added to it to induce cell growth
bridg:DefinedMaterialProcessStep.producedMaterial
have produced
bridg:DefinedMaterialProcessStep.producedMaterial
none
bridg:DefinedMaterialProcessStep.producedMaterial
producedMaterial
bridg:Material.producingPerformedMaterialProcessStep
have been produced by
bridg:Material.producingPerformedMaterialProcessStep
none
bridg:Material.producingPerformedMaterialProcessStep
producingPerformedMaterialProcessStep
bridg:Material.producingPerformedMaterialProcessStep
false
bridg:Material.producingPerformedMaterialProcessStep
Indicates that material was produced by a process step.
bridg:Material.producingPerformedMaterialProcessStep
A blood product has anticoagulants added to it to preserve the product
bridg:Material.producingPerformedMaterialProcessStep
A blood product has growth factor added to it to induce cell growth
bridg:PerformedMaterialProcessStep.producedMaterial
have produced
bridg:PerformedMaterialProcessStep.producedMaterial
none
bridg:PerformedMaterialProcessStep.producedMaterial
producedMaterial
bridg:MaterialIdentifier.assigningOrganization
be assigned by
bridg:MaterialIdentifier.assigningOrganization
none
bridg:MaterialIdentifier.assigningOrganization
assigningOrganization
bridg:MaterialIdentifier.assigningOrganization
false
bridg:MaterialIdentifier.assigningOrganization
Organization
bridg:MaterialIdentifier.assigningOrganization
urn:CTRv1.0:MaterialIdentifier.assigning
bridg:Organization.assignedMaterialIdentifier
assign
bridg:Organization.assignedMaterialIdentifier
none
bridg:Organization.assignedMaterialIdentifier
assignedMaterialIdentifier
bridg:MaterialIdentifier.identifiedMaterial
identifies
bridg:MaterialIdentifier.identifiedMaterial
none
bridg:MaterialIdentifier.identifiedMaterial
identifiedMaterial
bridg:MaterialIdentifier.identifiedMaterial
false
bridg:MaterialIdentifier.identifiedMaterial
Material
bridg:MaterialIdentifier.identifiedMaterial
urn:CTRv1.0:MaterialIdentifier.identified
bridg:Material.identifyingMaterialIdentifier
be identified by
bridg:Material.identifyingMaterialIdentifier
none
bridg:Material.identifyingMaterialIdentifier
identifyingMaterialIdentifier
bridg:MaterialName.approvingRegulatoryAuthority
be approved by
bridg:MaterialName.approvingRegulatoryAuthority
none
bridg:MaterialName.approvingRegulatoryAuthority
approvingRegulatoryAuthority
bridg:MaterialName.approvingRegulatoryAuthority
false
bridg:MaterialName.approvingRegulatoryAuthority
RegulatoryAuthority
bridg:MaterialName.approvingRegulatoryAuthority
urn:CTRv1.0:MaterialName.approving
bridg:RegulatoryAuthority.approvedMaterialName
approve
bridg:RegulatoryAuthority.approvedMaterialName
none
bridg:RegulatoryAuthority.approvedMaterialName
approvedMaterialName
bridg:MaterialName.namedMaterial
names
bridg:MaterialName.namedMaterial
none
bridg:MaterialName.namedMaterial
namedMaterial
bridg:MaterialName.namedMaterial
false
bridg:MaterialName.namedMaterial
Material
bridg:MaterialName.namedMaterial
urn:CTRv1.0:MaterialName.named
bridg:Material.namingMaterialName
is named by
bridg:Material.namingMaterialName
none
bridg:Material.namingMaterialName
namingMaterialName
bridg:NotificationReceiver.performingDocumentAuthor
be a function performed by
bridg:NotificationReceiver.performingDocumentAuthor
none
bridg:NotificationReceiver.performingDocumentAuthor
performingDocumentAuthor
bridg:NotificationReceiver.performingDocumentAuthor
false
bridg:NotificationReceiver.performingDocumentAuthor
bridg:DocumentAuthor.performedNotificationReceiver
function as
bridg:DocumentAuthor.performedNotificationReceiver
none
bridg:DocumentAuthor.performedNotificationReceiver
performedNotificationReceiver
bridg:NotificationReceiver.performingHealthcareProvider
be a function performed by
bridg:NotificationReceiver.performingHealthcareProvider
none
bridg:NotificationReceiver.performingHealthcareProvider
performingHealthcareProvider
bridg:NotificationReceiver.performingHealthcareProvider
false
bridg:NotificationReceiver.performingHealthcareProvider
bridg:HealthcareProvider.performedNotificationReceiver
function as
bridg:HealthcareProvider.performedNotificationReceiver
none
bridg:HealthcareProvider.performedNotificationReceiver
performedNotificationReceiver
bridg:NotificationReceiver.performingOrganization
be a function performed by
bridg:NotificationReceiver.performingOrganization
none
bridg:NotificationReceiver.performingOrganization
performingOrganization
bridg:NotificationReceiver.performingOrganization
false
bridg:NotificationReceiver.performingOrganization
bridg:Organization.performedNotificationReceiver
function as
bridg:Organization.performedNotificationReceiver
none
bridg:Organization.performedNotificationReceiver
performedNotificationReceiver
bridg:NotificationReceiver.performingReportSubmitter
be a function performed by
bridg:NotificationReceiver.performingReportSubmitter
none
bridg:NotificationReceiver.performingReportSubmitter
performingReportSubmitter
bridg:NotificationReceiver.performingReportSubmitter
false
bridg:NotificationReceiver.performingReportSubmitter
bridg:ReportSubmitter.performedNotificationReceiver
function as
bridg:ReportSubmitter.performedNotificationReceiver
none
bridg:ReportSubmitter.performedNotificationReceiver
performedNotificationReceiver
bridg:NotificationReceiver.performingStudyPersonnel
be a function performed by
bridg:NotificationReceiver.performingStudyPersonnel
none
bridg:NotificationReceiver.performingStudyPersonnel
performingStudyPersonnel
bridg:NotificationReceiver.performingStudyPersonnel
false
bridg:NotificationReceiver.performingStudyPersonnel
bridg:StudyPersonnel.performedNotificationReceiver
function as
bridg:StudyPersonnel.performedNotificationReceiver
none
bridg:StudyPersonnel.performedNotificationReceiver
performedNotificationReceiver
bridg:NotificationReceiver.performingStudySitePersonnel
be a function performed by
bridg:NotificationReceiver.performingStudySitePersonnel
none
bridg:NotificationReceiver.performingStudySitePersonnel
performingStudySitePersonnel
bridg:NotificationReceiver.performingStudySitePersonnel
false
bridg:NotificationReceiver.performingStudySitePersonnel
bridg:StudySitePersonnel.performedNotificationReceiver
function as
bridg:StudySitePersonnel.performedNotificationReceiver
none
bridg:StudySitePersonnel.performedNotificationReceiver
performedNotificationReceiver
bridg:NotificationReceiver.receivedDefinedNotification
be the receiver of
bridg:NotificationReceiver.receivedDefinedNotification
none
bridg:NotificationReceiver.receivedDefinedNotification
receivedDefinedNotification
bridg:NotificationReceiver.receivedDefinedNotification
false
bridg:NotificationReceiver.receivedDefinedNotification
bridg:DefinedNotification.receivingNotificationReceiver
be received by
bridg:DefinedNotification.receivingNotificationReceiver
none
bridg:DefinedNotification.receivingNotificationReceiver
receivingNotificationReceiver
bridg:NotificationReceiver.receivedPerformedNotification
be the receiver of
bridg:NotificationReceiver.receivedPerformedNotification
none
bridg:NotificationReceiver.receivedPerformedNotification
receivedPerformedNotification
bridg:NotificationReceiver.receivedPerformedNotification
false
bridg:NotificationReceiver.receivedPerformedNotification
bridg:PerformedNotification.receivingNotificationReceiver
be received by
bridg:PerformedNotification.receivingNotificationReceiver
none
bridg:PerformedNotification.receivingNotificationReceiver
receivingNotificationReceiver
bridg:NotificationReceiver.receivedPlannedNotification
be the receiver of
bridg:NotificationReceiver.receivedPlannedNotification
none
bridg:NotificationReceiver.receivedPlannedNotification
receivedPlannedNotification
bridg:NotificationReceiver.receivedPlannedNotification
false
bridg:NotificationReceiver.receivedPlannedNotification
bridg:PlannedNotification.receivingNotificationReceiver
be received by
bridg:PlannedNotification.receivingNotificationReceiver
none
bridg:PlannedNotification.receivingNotificationReceiver
receivingNotificationReceiver
bridg:NotificationReceiver.receivedScheduledNotification
be the receiver of
bridg:NotificationReceiver.receivedScheduledNotification
none
bridg:NotificationReceiver.receivedScheduledNotification
receivedScheduledNotification
bridg:NotificationReceiver.receivedScheduledNotification
false
bridg:NotificationReceiver.receivedScheduledNotification
bridg:ScheduledNotification.receivingNotificationReceiver
be received by
bridg:ScheduledNotification.receivingNotificationReceiver
none
bridg:ScheduledNotification.receivingNotificationReceiver
receivingNotificationReceiver
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
triggers
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
none
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
triggeredPerformedActivity
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
false
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
Indicates the PerformedActivity undertaken as a result of an ObservationResult
PerformedActivity
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
urn:CTRv1.0:ObservationResultActionTakenRelationship.triggered
PerformedActivity
bridg:ObservationResultActionTakenRelationship.triggeredPerformedActivity
urn:CTRv1.0:ProductActionTakenRelationship.triggered
bridg:PerformedActivity.triggeringObservationResultActionTakenRelationship
be triggered by
bridg:PerformedActivity.triggeringObservationResultActionTakenRelationship
none
bridg:PerformedActivity.triggeringObservationResultActionTakenRelationship
triggeringObservationResultActionTakenRelationship
bridg:ObservationResultActionTakenRelationship.triggeringPerformedObservationResult
is triggered by
bridg:ObservationResultActionTakenRelationship.triggeringPerformedObservationResult
none
bridg:ObservationResultActionTakenRelationship.triggeringPerformedObservationResult
triggeringPerformedObservationResult
bridg:ObservationResultActionTakenRelationship.triggeringPerformedObservationResult
false
bridg:ObservationResultActionTakenRelationship.triggeringPerformedObservationResult
Indicates the ObservationResult that causes the initiation of a PerformedActivity
PerformedObservationResult
bridg:ObservationResultActionTakenRelationship.triggeringPerformedObservationResult
urn:CTRv1.0:ObservationResultActionTakenRelationship.triggering
bridg:PerformedObservationResult.triggeredObservationResultActionTakenRelationship
trigger
bridg:PerformedObservationResult.triggeredObservationResultActionTakenRelationship
none
bridg:PerformedObservationResult.triggeredObservationResultActionTakenRelationship
triggeredObservationResultActionTakenRelationship
bridg:OrganizationIdentifier.assigningOrganization
be assigned by
bridg:OrganizationIdentifier.assigningOrganization
none
bridg:OrganizationIdentifier.assigningOrganization
assigningOrganization
bridg:OrganizationIdentifier.assigningOrganization
false
bridg:OrganizationIdentifier.assigningOrganization
Organization
bridg:OrganizationIdentifier.assigningOrganization
urn:CTRv1.0:OrganizationIdentifier.assigning
bridg:Organization.assignedOrganizationIdentifier
assign
bridg:Organization.assignedOrganizationIdentifier
none
bridg:Organization.assignedOrganizationIdentifier
assignedOrganizationIdentifier
bridg:OrganizationIdentifier.assigningSystemOfRecord
be assigned by
bridg:OrganizationIdentifier.assigningSystemOfRecord
none
bridg:OrganizationIdentifier.assigningSystemOfRecord
assigningSystemOfRecord
bridg:OrganizationIdentifier.assigningSystemOfRecord
false
bridg:OrganizationIdentifier.assigningSystemOfRecord
SystemOfRecord
bridg:OrganizationIdentifier.assigningSystemOfRecord
urn:CTRv1.0:OrganizationIdentifier.assigning
bridg:SystemOfRecord.assignedOrganizationIdentifier
assign
bridg:SystemOfRecord.assignedOrganizationIdentifier
none
bridg:SystemOfRecord.assignedOrganizationIdentifier
assignedOrganizationIdentifier
bridg:OrganizationIdentifier.identifiedOrganization
identifies
bridg:OrganizationIdentifier.identifiedOrganization
none
bridg:OrganizationIdentifier.identifiedOrganization
identifiedOrganization
bridg:OrganizationIdentifier.identifiedOrganization
false
bridg:OrganizationIdentifier.identifiedOrganization
IdentifiedEntity
bridg:OrganizationIdentifier.identifiedOrganization
urn:CTRPv3.8:Organization.
Organization
bridg:OrganizationIdentifier.identifiedOrganization
urn:CTRv1.0:OrganizationIdentifier.identified
bridg:Organization.identifyingOrganizationIdentifier
be identified by
bridg:Organization.identifyingOrganizationIdentifier
none
bridg:Organization.identifyingOrganizationIdentifier
identifyingOrganizationIdentifier
bridg:OrganizationRelationship.sourceOrganization
has as source
bridg:OrganizationRelationship.sourceOrganization
none
bridg:OrganizationRelationship.sourceOrganization
sourceOrganization
bridg:OrganizationRelationship.sourceOrganization
false
bridg:OrganizationRelationship.sourceOrganization
OrganizationalGroup
bridg:OrganizationRelationship.sourceOrganization
urn:CTRPv3.8:OrganizationalGroupRelationship.
Organization
bridg:OrganizationRelationship.sourceOrganization
urn:CTRv1.0:OrganizationRelationship.source
bridg:Organization.targetOrganizationRelationship
be the source for
bridg:Organization.targetOrganizationRelationship
none
bridg:Organization.targetOrganizationRelationship
targetOrganizationRelationship
bridg:OrganizationRelationship.targetOrganization
has as target
bridg:OrganizationRelationship.targetOrganization
none
bridg:OrganizationRelationship.targetOrganization
targetOrganization
bridg:OrganizationRelationship.targetOrganization
false
bridg:OrganizationRelationship.targetOrganization
OrganizationalGroupRelationship
bridg:OrganizationRelationship.targetOrganization
urn:CTRPv3.8:Organization.
OrganizationalRelationship
bridg:OrganizationRelationship.targetOrganization
urn:CTRPv3.8:Organization.
Organization
bridg:OrganizationRelationship.targetOrganization
urn:CTRv1.0:OrganizationRelationship.target
bridg:Organization.sourceOrganizationRelationship
be the target for
bridg:Organization.sourceOrganizationRelationship
none
bridg:Organization.sourceOrganizationRelationship
sourceOrganizationRelationship
bridg:OrganizationalContact.performingPerson
be a function performed by
bridg:OrganizationalContact.performingPerson
none
bridg:OrganizationalContact.performingPerson
performingPerson
bridg:OrganizationalContact.performingPerson
false
bridg:OrganizationalContact.performingPerson
Person
bridg:OrganizationalContact.performingPerson
urn:CTRv1.0:OrganizationalContact.performing
bridg:Person.performedOrganizationalContact
function as
bridg:Person.performedOrganizationalContact
none
bridg:Person.performedOrganizationalContact
performedOrganizationalContact
bridg:OrganizationalContact.supportedOrganization
handles communication for
bridg:OrganizationalContact.supportedOrganization
none
bridg:OrganizationalContact.supportedOrganization
supportedOrganization
bridg:OrganizationalContact.supportedOrganization
false
bridg:OrganizationalContact.supportedOrganization
Organization
bridg:OrganizationalContact.supportedOrganization
urn:CTRv1.0:OrganizationalContact.supported
bridg:Organization.supportingOrganizationalContact
have communications handled by
bridg:Organization.supportingOrganizationalContact
none
bridg:Organization.supportingOrganizationalContact
supportingOrganizationalContact
bridg:OversightAuthority.performingOrganization
is a function performed by
bridg:OversightAuthority.performingOrganization
none
bridg:OversightAuthority.performingOrganization
performingOrganization
bridg:OversightAuthority.performingOrganization
false
bridg:OversightAuthority.performingOrganization
Organization
bridg:OversightAuthority.performingOrganization
urn:CTRRr3:OversightAuthority.performing
Organization
bridg:OversightAuthority.performingOrganization
urn:CTRv1.0:OversightAuthority.performing
bridg:Organization.performedOversightAuthority
function as
bridg:Organization.performedOversightAuthority
none
bridg:Organization.performedOversightAuthority
performedOversightAuthority
bridg:OversightCommittee.overseenHealthcareFacility
oversee
bridg:OversightCommittee.overseenHealthcareFacility
none
bridg:OversightCommittee.overseenHealthcareFacility
overseenHealthcareFacility
bridg:OversightCommittee.overseenHealthcareFacility
false
bridg:OversightCommittee.overseenHealthcareFacility
HealthcareFacility
bridg:OversightCommittee.overseenHealthcareFacility
urn:CTRv1.0:OversightCommittee.overseen
bridg:HealthcareFacility.overseeingOversightCommittee
be overseen by
bridg:HealthcareFacility.overseeingOversightCommittee
none
bridg:HealthcareFacility.overseeingOversightCommittee
overseeingOversightCommittee
bridg:OversightCommittee.overseenStudySite
oversee
bridg:OversightCommittee.overseenStudySite
none
bridg:OversightCommittee.overseenStudySite
overseenStudySite
bridg:OversightCommittee.overseenStudySite
false
bridg:OversightCommittee.overseenStudySite
StudySite
bridg:OversightCommittee.overseenStudySite
urn:CTRPv3.8:OversightCommittee.
StudySite
bridg:OversightCommittee.overseenStudySite
urn:CTRRr3:OversightCommittee.overseen
StudySite
bridg:OversightCommittee.overseenStudySite
urn:CTRv1.0:OversightCommittee.overseen
bridg:StudySite.overseeingOversightCommittee
be overseen by
bridg:StudySite.overseeingOversightCommittee
none
bridg:StudySite.overseeingOversightCommittee
overseeingOversightCommittee
bridg:PerformedActivity.containingEpoch
be contained by
bridg:PerformedActivity.containingEpoch
none
bridg:PerformedActivity.containingEpoch
containingEpoch
bridg:PerformedActivity.containingEpoch
false
bridg:PerformedActivity.containingEpoch
Indicates that a performed but unplanned activity is categorized as part of a particular Epoch.
bridg:PerformedActivity.containingEpoch
This cannot be derived by looking at the corresponding planned activity because this association is only used for unplanned activities.
PerformedActivity
bridg:PerformedActivity.containingEpoch
urn:CTRPv3.8:Epoch.
Epoch
bridg:PerformedActivity.containingEpoch
urn:CTRv1.0:PerformedActivity.containing
bridg:Epoch.containedPerformedActivity
contain
bridg:Epoch.containedPerformedActivity
none
bridg:Epoch.containedPerformedActivity
containedPerformedActivity
bridg:PerformedActivity.instantiatedDefinedActivity
instantiate
bridg:PerformedActivity.instantiatedDefinedActivity
none
bridg:PerformedActivity.instantiatedDefinedActivity
instantiatedDefinedActivity
bridg:PerformedActivity.instantiatedDefinedActivity
false
bridg:PerformedActivity.instantiatedDefinedActivity
bridg:PerformedActivity.instantiatedDefinedActivity
urn:CTOM:Radiation.scheduleText
DefinedActivity
bridg:PerformedActivity.instantiatedDefinedActivity
urn:CTRv1.0:PerformedActivity.instantiated
bridg:DefinedActivity.instantiatingPerformedActivity
be instantiated by
bridg:DefinedActivity.instantiatingPerformedActivity
none
bridg:DefinedActivity.instantiatingPerformedActivity
instantiatingPerformedActivity
bridg:PerformedActivity.instantiatedPlannedActivity
instantiate
bridg:PerformedActivity.instantiatedPlannedActivity
none
bridg:PerformedActivity.instantiatedPlannedActivity
instantiatedPlannedActivity
bridg:PerformedActivity.instantiatedPlannedActivity
false
bridg:PerformedActivity.instantiatedPlannedActivity
PlannedActivity
bridg:PerformedActivity.instantiatedPlannedActivity
urn:CTRv1.0:PerformedActivity.instantiated
bridg:PlannedActivity.instantiatingPerformedActivity
be instantiated by
bridg:PlannedActivity.instantiatingPerformedActivity
none
bridg:PlannedActivity.instantiatingPerformedActivity
instantiatingPerformedActivity
bridg:PerformedActivity.instantiatedScheduledActivity
instantiate
bridg:PerformedActivity.instantiatedScheduledActivity
none
bridg:PerformedActivity.instantiatedScheduledActivity
instantiatedScheduledActivity
bridg:PerformedActivity.instantiatedScheduledActivity
false
bridg:PerformedActivity.instantiatedScheduledActivity
bridg:ScheduledActivity.instantiatingPerformedActivity
be instantiated by
bridg:ScheduledActivity.instantiatingPerformedActivity
none
bridg:ScheduledActivity.instantiatingPerformedActivity
instantiatingPerformedActivity
bridg:PerformedActivity.locatingPlace
take place in
bridg:PerformedActivity.locatingPlace
none
bridg:PerformedActivity.locatingPlace
locatingPlace
bridg:PerformedActivity.locatingPlace
false
bridg:PerformedActivity.locatingPlace
Place
bridg:PerformedActivity.locatingPlace
urn:CTRv1.0:PerformedActivity.locating
bridg:Place.locatedPerformedActivity
be the location for
bridg:Place.locatedPerformedActivity
none
bridg:Place.locatedPerformedActivity
locatedPerformedActivity
bridg:PerformedActivity.versionStudyProtocolVersion
execute under
bridg:PerformedActivity.versionStudyProtocolVersion
none
bridg:PerformedActivity.versionStudyProtocolVersion
versionStudyProtocolVersion
bridg:PerformedActivity.versionStudyProtocolVersion
false
bridg:PerformedActivity.versionStudyProtocolVersion
StudyProtocolVersion
bridg:PerformedActivity.versionStudyProtocolVersion
urn:CTRv1.0:PerformedActivity.version
bridg:StudyProtocolVersion.executedPerformedActivity
be executed by
bridg:StudyProtocolVersion.executedPerformedActivity
none
bridg:StudyProtocolVersion.executedPerformedActivity
executedPerformedActivity
bridg:PerformedAdministrativeActivity.performingStudySite
be performed at
bridg:PerformedAdministrativeActivity.performingStudySite
none
bridg:PerformedAdministrativeActivity.performingStudySite
performingStudySite
bridg:PerformedAdministrativeActivity.performingStudySite
false
bridg:PerformedAdministrativeActivity.performingStudySite
StudySite
bridg:PerformedAdministrativeActivity.performingStudySite
urn:CTRv1.0:PerformedAdministrativeActivity.performing
bridg:StudySite.performedPerformedAdministrativeActivity
perform
bridg:StudySite.performedPerformedAdministrativeActivity
none
bridg:StudySite.performedPerformedAdministrativeActivity
performedPerformedAdministrativeActivity
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
be converted into
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
none
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
convertedPerformedClinicalResult
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
false
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
urn:CTOM:ObservationRelationship
PerformedClinicalResult
bridg:PerformedClinicalResult.convertedPerformedClinicalResult
urn:CTRv1.0:PerformedClinicalResult.canonical
bridg:PerformedClinicalResult.originalPerformedClinicalResult
be converted from
bridg:PerformedClinicalResult.originalPerformedClinicalResult
none
bridg:PerformedClinicalResult.originalPerformedClinicalResult
originalPerformedClinicalResult
bridg:PerformedClinicalResult.referencedReferenceResult
reference
bridg:PerformedClinicalResult.referencedReferenceResult
none
bridg:PerformedClinicalResult.referencedReferenceResult
referencedReferenceResult
bridg:PerformedClinicalResult.referencedReferenceResult
false
bridg:PerformedClinicalResult.referencedReferenceResult
ReferenceResult
bridg:PerformedClinicalResult.referencedReferenceResult
urn:CTRv1.0:PerformedClinicalResult.referenced
bridg:ReferenceResult.referencingPerformedClinicalResult
be referenced by
bridg:ReferenceResult.referencingPerformedClinicalResult
none
bridg:ReferenceResult.referencingPerformedClinicalResult
referencingPerformedClinicalResult
bridg:PerformedCompositionRelationship.componentPerformedActivity
is the parent of
bridg:PerformedCompositionRelationship.componentPerformedActivity
none
bridg:PerformedCompositionRelationship.componentPerformedActivity
componentPerformedActivity
bridg:PerformedCompositionRelationship.componentPerformedActivity
false
bridg:PerformedCompositionRelationship.componentPerformedActivity
bridg:PerformedActivity.compositePerformedCompositionRelationship
be the component of
bridg:PerformedActivity.compositePerformedCompositionRelationship
none
bridg:PerformedActivity.compositePerformedCompositionRelationship
compositePerformedCompositionRelationship
bridg:PerformedCompositionRelationship.compositePerformedActivity
is the component of
bridg:PerformedCompositionRelationship.compositePerformedActivity
none
bridg:PerformedCompositionRelationship.compositePerformedActivity
compositePerformedActivity
bridg:PerformedCompositionRelationship.compositePerformedActivity
false
bridg:PerformedCompositionRelationship.compositePerformedActivity
bridg:PerformedActivity.componentPerformedCompositionRelationship
be the parent of
bridg:PerformedActivity.componentPerformedCompositionRelationship
none
bridg:PerformedActivity.componentPerformedCompositionRelationship
componentPerformedCompositionRelationship
bridg:PerformedDiagnosis.transformedPerformedDiagnosis
be transformed into
bridg:PerformedDiagnosis.transformedPerformedDiagnosis
none
bridg:PerformedDiagnosis.transformedPerformedDiagnosis
transformedPerformedDiagnosis
bridg:PerformedDiagnosis.transformedPerformedDiagnosis
false
bridg:PerformedDiagnosis.transformedPerformedDiagnosis
bridg:PerformedDiagnosis.transformingPerformedDiagnosis
be transformed from
bridg:PerformedDiagnosis.transformingPerformedDiagnosis
none
bridg:PerformedDiagnosis.transformingPerformedDiagnosis
transformingPerformedDiagnosis
bridg:PerformedDiagnosisProcedureRelationship.addressedPerformedDiagnosis
addresses
bridg:PerformedDiagnosisProcedureRelationship.addressedPerformedDiagnosis
none
bridg:PerformedDiagnosisProcedureRelationship.addressedPerformedDiagnosis
addressedPerformedDiagnosis
bridg:PerformedDiagnosisProcedureRelationship.addressedPerformedDiagnosis
false
bridg:PerformedDiagnosisProcedureRelationship.addressedPerformedDiagnosis
bridg:PerformedDiagnosis.addressingPerformedDiagnosisProcedureRelationship
be addressed by
bridg:PerformedDiagnosis.addressingPerformedDiagnosisProcedureRelationship
none
bridg:PerformedDiagnosis.addressingPerformedDiagnosisProcedureRelationship
addressingPerformedDiagnosisProcedureRelationship
bridg:PerformedDiagnosisProcedureRelationship.addressingPerformedProcedure
is addressed by
bridg:PerformedDiagnosisProcedureRelationship.addressingPerformedProcedure
none
bridg:PerformedDiagnosisProcedureRelationship.addressingPerformedProcedure
addressingPerformedProcedure
bridg:PerformedDiagnosisProcedureRelationship.addressingPerformedProcedure
false
bridg:PerformedDiagnosisProcedureRelationship.addressingPerformedProcedure
bridg:PerformedProcedure.addressedPerformedDiagnosisProcedureRelationship
address
bridg:PerformedProcedure.addressedPerformedDiagnosisProcedureRelationship
none
bridg:PerformedProcedure.addressedPerformedDiagnosisProcedureRelationship
addressedPerformedDiagnosisProcedureRelationship
bridg:PerformedExperimentalUnitAllocation.assignedArm
assign a subject to
bridg:PerformedExperimentalUnitAllocation.assignedArm
none
bridg:PerformedExperimentalUnitAllocation.assignedArm
assignedArm
bridg:PerformedExperimentalUnitAllocation.assignedArm
false
bridg:PerformedExperimentalUnitAllocation.assignedArm
Arm
bridg:PerformedExperimentalUnitAllocation.assignedArm
urn:CTRv1.0:StudySubject.intended
bridg:Arm.assigningPerformedExperimentalUnitAllocation
be assigned a subject by
bridg:Arm.assigningPerformedExperimentalUnitAllocation
none
bridg:Arm.assigningPerformedExperimentalUnitAllocation
assigningPerformedExperimentalUnitAllocation
bridg:PerformedObservation.commentedPerformedActivity
be commenting on
bridg:PerformedObservation.commentedPerformedActivity
none
bridg:PerformedObservation.commentedPerformedActivity
commentedPerformedActivity
bridg:PerformedObservation.commentedPerformedActivity
false
bridg:PerformedObservation.commentedPerformedActivity
PerformedActivity
bridg:PerformedObservation.commentedPerformedActivity
urn:CTRv1.0:PerformedObservation.commented
bridg:PerformedActivity.commentingPerformedObservation
be commented on by
bridg:PerformedActivity.commentingPerformedObservation
none
bridg:PerformedActivity.commentingPerformedObservation
commentingPerformedObservation
bridg:PerformedObservation.commentedSafetyReportVersion
be commenting on
bridg:PerformedObservation.commentedSafetyReportVersion
none
bridg:PerformedObservation.commentedSafetyReportVersion
commentedSafetyReportVersion
bridg:PerformedObservation.commentedSafetyReportVersion
false
bridg:PerformedObservation.commentedSafetyReportVersion
SafetyReportVersion
bridg:PerformedObservation.commentedSafetyReportVersion
urn:CTRv1.0:PerformedObservation.commented
bridg:SafetyReportVersion.commentingPerformedObservation
be commented on by
bridg:SafetyReportVersion.commentingPerformedObservation
none
bridg:SafetyReportVersion.commentingPerformedObservation
commentingPerformedObservation
bridg:PerformedObservation.performingPerformingLaboratory
be performed by
bridg:PerformedObservation.performingPerformingLaboratory
none
bridg:PerformedObservation.performingPerformingLaboratory
performingPerformingLaboratory
bridg:PerformedObservation.performingPerformingLaboratory
false
bridg:PerformedObservation.performingPerformingLaboratory
PerformingLaboratory
bridg:PerformedObservation.performingPerformingLaboratory
urn:CTRv1.0:PerformedObservation.performing
bridg:PerformingLaboratory.performedPerformedObservation
perform
bridg:PerformingLaboratory.performedPerformedObservation
none
bridg:PerformingLaboratory.performedPerformedObservation
performedPerformedObservation
bridg:PerformedObservation.reportingAssessor
be reported by
bridg:PerformedObservation.reportingAssessor
none
bridg:PerformedObservation.reportingAssessor
reportingAssessor
bridg:PerformedObservation.reportingAssessor
false
bridg:PerformedObservation.reportingAssessor
Assessor
bridg:PerformedObservation.reportingAssessor
urn:CTRv1.0:PerformedObservation.reporting
bridg:Assessor.reportedPerformedObservation
report
bridg:Assessor.reportedPerformedObservation
none
bridg:Assessor.reportedPerformedObservation
reportedPerformedObservation
bridg:PerformedObservationResult.infersPerformedObservationResult
be inferred from
bridg:PerformedObservationResult.infersPerformedObservationResult
none
bridg:PerformedObservationResult.infersPerformedObservationResult
infersPerformedObservationResult
bridg:PerformedObservationResult.infersPerformedObservationResult
false
bridg:PerformedObservationResult.infersPerformedObservationResult
PerformedObservationResult
bridg:PerformedObservationResult.infersPerformedObservationResult
urn:CTRv1.0:PerformedObservationResult.infers
bridg:PerformedObservationResult.inferredPerformedObservationResult
infer
bridg:PerformedObservationResult.inferredPerformedObservationResult
none
bridg:PerformedObservationResult.inferredPerformedObservationResult
inferredPerformedObservationResult
bridg:PerformedObservationResult.producingPerformedObservation
is a result of
bridg:PerformedObservationResult.producingPerformedObservation
none
bridg:PerformedObservationResult.producingPerformedObservation
producingPerformedObservation
bridg:PerformedObservationResult.producingPerformedObservation
false
bridg:PerformedObservationResult.producingPerformedObservation
PerformedObservationResult
bridg:PerformedObservationResult.producingPerformedObservation
urn:CTRPv3.8:PerformedObservation.
PerformedObservation
bridg:PerformedObservationResult.producingPerformedObservation
urn:CTRv1.0:PerformedObservationResult.producing
bridg:PerformedObservation.resultedPerformedObservationResult
result in
bridg:PerformedObservation.resultedPerformedObservationResult
none
bridg:PerformedObservation.resultedPerformedObservationResult
resultedPerformedObservationResult
bridg:PerformedProcedure.triggeringPerformedObservationResult
be recorded as a result of
bridg:PerformedProcedure.triggeringPerformedObservationResult
none
bridg:PerformedProcedure.triggeringPerformedObservationResult
triggeringPerformedObservationResult
bridg:PerformedProcedure.triggeringPerformedObservationResult
false
bridg:PerformedProcedure.triggeringPerformedObservationResult
PerformedObservationResult
bridg:PerformedProcedure.triggeringPerformedObservationResult
urn:CTRv1.0:PerformedProcedure.triggering
bridg:PerformedObservationResult.recordedPerformedProcedure
result in recording
bridg:PerformedObservationResult.recordedPerformedProcedure
none
bridg:PerformedObservationResult.recordedPerformedProcedure
recordedPerformedProcedure
bridg:PerformedProcedure.usedProduct
use
bridg:PerformedProcedure.usedProduct
none
bridg:PerformedProcedure.usedProduct
usedProduct
bridg:PerformedProcedure.usedProduct
false
bridg:PerformedProcedure.usedProduct
StudyAgent
bridg:PerformedProcedure.usedProduct
urn:CTRv1.0:PerformedProcedure.used
bridg:Product.usingPerformedProcedure
be used during
bridg:Product.usingPerformedProcedure
none
bridg:Product.usingPerformedProcedure
usingPerformedProcedure
bridg:PerformedProductInvestigation.triggeringAdverseEvent
is triggered by
bridg:PerformedProductInvestigation.triggeringAdverseEvent
none
bridg:PerformedProductInvestigation.triggeringAdverseEvent
triggeringAdverseEvent
bridg:PerformedProductInvestigation.triggeringAdverseEvent
false
bridg:PerformedProductInvestigation.triggeringAdverseEvent
AdverseEvent
bridg:PerformedProductInvestigation.triggeringAdverseEvent
urn:CTRv1.0:PerformedProductInvestigation.triggering
bridg:AdverseEvent.triggeredPerformedProductInvestigation
trigger
bridg:AdverseEvent.triggeredPerformedProductInvestigation
none
bridg:AdverseEvent.triggeredPerformedProductInvestigation
triggeredPerformedProductInvestigation
bridg:PerformedProductInvestigation.triggeringPerformedProductProblemDiscovery
is triggered by
bridg:PerformedProductInvestigation.triggeringPerformedProductProblemDiscovery
none
bridg:PerformedProductInvestigation.triggeringPerformedProductProblemDiscovery
triggeringPerformedProductProblemDiscovery
bridg:PerformedProductInvestigation.triggeringPerformedProductProblemDiscovery
false
bridg:PerformedProductInvestigation.triggeringPerformedProductProblemDiscovery
PerformedProductProblemDiscovery
bridg:PerformedProductInvestigation.triggeringPerformedProductProblemDiscovery
urn:CTRv1.0:PerformedProductInvestigation.triggering
bridg:PerformedProductProblemDiscovery.triggeredPerformedProductInvestigation
trigger
bridg:PerformedProductProblemDiscovery.triggeredPerformedProductInvestigation
none
bridg:PerformedProductProblemDiscovery.triggeredPerformedProductInvestigation
triggeredPerformedProductInvestigation
bridg:PerformedProductProblemDiscovery.involvedProduct
focuses on
bridg:PerformedProductProblemDiscovery.involvedProduct
none
bridg:PerformedProductProblemDiscovery.involvedProduct
involvedProduct
bridg:PerformedProductProblemDiscovery.involvedProduct
false
bridg:PerformedProductProblemDiscovery.involvedProduct
Product
bridg:PerformedProductProblemDiscovery.involvedProduct
urn:CTRv1.0:PerformedProductProblemDiscovery.involved
bridg:Product.involvingPerformedProductProblemDiscovery
be the focus of
bridg:Product.involvingPerformedProductProblemDiscovery
none
bridg:Product.involvingPerformedProductProblemDiscovery
involvingPerformedProductProblemDiscovery
bridg:PerformedProductTransport.destinationServiceDeliveryLocation
have destination
bridg:PerformedProductTransport.destinationServiceDeliveryLocation
none
bridg:PerformedProductTransport.destinationServiceDeliveryLocation
destinationServiceDeliveryLocation
bridg:PerformedProductTransport.destinationServiceDeliveryLocation
false
bridg:PerformedProductTransport.destinationServiceDeliveryLocation
ServiceDeliveryLocation
bridg:PerformedProductTransport.destinationServiceDeliveryLocation
urn:CTRv1.0:PerformedProductTransport.destination
bridg:ServiceDeliveryLocation.destinedPerformedProductTransport
be the destination for
bridg:ServiceDeliveryLocation.destinedPerformedProductTransport
none
bridg:ServiceDeliveryLocation.destinedPerformedProductTransport
destinedPerformedProductTransport
bridg:PerformedProductTransport.originServiceDeliveryLocation
originate at
bridg:PerformedProductTransport.originServiceDeliveryLocation
none
bridg:PerformedProductTransport.originServiceDeliveryLocation
originServiceDeliveryLocation
bridg:PerformedProductTransport.originServiceDeliveryLocation
false
bridg:PerformedProductTransport.originServiceDeliveryLocation
ServiceDeliveryLocation
bridg:PerformedProductTransport.originServiceDeliveryLocation
urn:CTRv1.0:PerformedProductTransport.origin
bridg:ServiceDeliveryLocation.originatedPerformedProductTransport
be the origin of
bridg:ServiceDeliveryLocation.originatedPerformedProductTransport
none
bridg:ServiceDeliveryLocation.originatedPerformedProductTransport
originatedPerformedProductTransport
bridg:PerformedProtocolDeviation.authorizingStudyLegalSponsor
be authorized by
bridg:PerformedProtocolDeviation.authorizingStudyLegalSponsor
none
bridg:PerformedProtocolDeviation.authorizingStudyLegalSponsor
authorizingStudyLegalSponsor
bridg:PerformedProtocolDeviation.authorizingStudyLegalSponsor
false
bridg:PerformedProtocolDeviation.authorizingStudyLegalSponsor
StudyLegalSponsor
bridg:PerformedProtocolDeviation.authorizingStudyLegalSponsor
urn:CTRv1.0:PerformedProtocolDeviation.authorizing
bridg:StudyLegalSponsor.authorizedPerformedProtocolDeviation
authorize
bridg:StudyLegalSponsor.authorizedPerformedProtocolDeviation
none
bridg:StudyLegalSponsor.authorizedPerformedProtocolDeviation
authorizedPerformedProtocolDeviation
bridg:PerformedProtocolDeviation.implementingStudySitePersonnel
have management action implemented by
bridg:PerformedProtocolDeviation.implementingStudySitePersonnel
none
bridg:PerformedProtocolDeviation.implementingStudySitePersonnel
implementingStudySitePersonnel
bridg:PerformedProtocolDeviation.implementingStudySitePersonnel
false
bridg:PerformedProtocolDeviation.implementingStudySitePersonnel
bridg:StudySitePersonnel.implementedPerformedProtocolDeviation
implement the management action for
bridg:StudySitePersonnel.implementedPerformedProtocolDeviation
none
bridg:StudySitePersonnel.implementedPerformedProtocolDeviation
implementedPerformedProtocolDeviation
bridg:PerformedProtocolDeviation.managingStudyResearchCoordinator
have management action determined by
bridg:PerformedProtocolDeviation.managingStudyResearchCoordinator
none
bridg:PerformedProtocolDeviation.managingStudyResearchCoordinator
managingStudyResearchCoordinator
bridg:PerformedProtocolDeviation.managingStudyResearchCoordinator
false
bridg:PerformedProtocolDeviation.managingStudyResearchCoordinator
bridg:StudyResearchCoordinator.managedPerformedProtocolDeviation
determine the management action for
bridg:StudyResearchCoordinator.managedPerformedProtocolDeviation
none
bridg:StudyResearchCoordinator.managedPerformedProtocolDeviation
managedPerformedProtocolDeviation
bridg:PerformedSpecimenCollection.performingCollectingLaboratory
be performed by
bridg:PerformedSpecimenCollection.performingCollectingLaboratory
none
bridg:PerformedSpecimenCollection.performingCollectingLaboratory
performingCollectingLaboratory
bridg:PerformedSpecimenCollection.performingCollectingLaboratory
false
bridg:PerformedSpecimenCollection.performingCollectingLaboratory
bridg:CollectingLaboratory.performedPerformedSpecimenCollection
performs
bridg:CollectingLaboratory.performedPerformedSpecimenCollection
none
bridg:CollectingLaboratory.performedPerformedSpecimenCollection
performedPerformedSpecimenCollection
bridg:PerformedStudyAgentTransfer.authorizingStudySiteResearchCoordinator
be authorized by
bridg:PerformedStudyAgentTransfer.authorizingStudySiteResearchCoordinator
none
bridg:PerformedStudyAgentTransfer.authorizingStudySiteResearchCoordinator
authorizingStudySiteResearchCoordinator
bridg:PerformedStudyAgentTransfer.authorizingStudySiteResearchCoordinator
false
bridg:PerformedStudyAgentTransfer.authorizingStudySiteResearchCoordinator
bridg:StudySiteResearchCoordinator.authorizedPerformedStudyAgentTransfer
authorize
bridg:StudySiteResearchCoordinator.authorizedPerformedStudyAgentTransfer
none
bridg:StudySiteResearchCoordinator.authorizedPerformedStudyAgentTransfer
authorizedPerformedStudyAgentTransfer
bridg:PerformedStudyAgentTransfer.transferredProduct
is a transfer of
bridg:PerformedStudyAgentTransfer.transferredProduct
none
bridg:PerformedStudyAgentTransfer.transferredProduct
transferredProduct
bridg:PerformedStudyAgentTransfer.transferredProduct
false
bridg:PerformedStudyAgentTransfer.transferredProduct
StudyAgent
bridg:PerformedStudyAgentTransfer.transferredProduct
urn:CTRv1.0:PerformedStudyAgentTransfer.transferred
bridg:Product.transferringPerformedStudyAgentTransfer
be transferred during
bridg:Product.transferringPerformedStudyAgentTransfer
none
bridg:Product.transferringPerformedStudyAgentTransfer
transferringPerformedStudyAgentTransfer
bridg:PerformedStudySubjectMilestone.usedDocumentVersion
use
bridg:PerformedStudySubjectMilestone.usedDocumentVersion
none
bridg:PerformedStudySubjectMilestone.usedDocumentVersion
usedDocumentVersion
bridg:PerformedStudySubjectMilestone.usedDocumentVersion
false
bridg:PerformedStudySubjectMilestone.usedDocumentVersion
DocumentVersion
bridg:PerformedStudySubjectMilestone.usedDocumentVersion
urn:CTRv1.0:PerformedStudySubjectMilestone.used
bridg:DocumentVersion.usingPerformedStudySubjectMilestone
be used for
bridg:DocumentVersion.usingPerformedStudySubjectMilestone
none
bridg:DocumentVersion.usingPerformedStudySubjectMilestone
usingPerformedStudySubjectMilestone
bridg:PerformedSubstanceAdministration.addressedPerformedMedicalConditionResult
address
bridg:PerformedSubstanceAdministration.addressedPerformedMedicalConditionResult
none
bridg:PerformedSubstanceAdministration.addressedPerformedMedicalConditionResult
addressedPerformedMedicalConditionResult
bridg:PerformedSubstanceAdministration.addressedPerformedMedicalConditionResult
false
bridg:PerformedSubstanceAdministration.addressedPerformedMedicalConditionResult
PerformedMedicalConditionResult
bridg:PerformedSubstanceAdministration.addressedPerformedMedicalConditionResult
urn:CTRv1.0:PerformedSubstanceAdministration.addressed
bridg:PerformedMedicalConditionResult.addressingPerformedSubstanceAdministration
be addressed by
bridg:PerformedMedicalConditionResult.addressingPerformedSubstanceAdministration
none
bridg:PerformedMedicalConditionResult.addressingPerformedSubstanceAdministration
addressingPerformedSubstanceAdministration
bridg:PerformedSubstanceExtraction.producedBiologic
produces
bridg:PerformedSubstanceExtraction.producedBiologic
none
bridg:PerformedSubstanceExtraction.producedBiologic
producedBiologic
bridg:PerformedSubstanceExtraction.producedBiologic
false
bridg:PerformedSubstanceExtraction.producedBiologic
bridg:Biologic.producingPerformedSubstanceExtraction
be produced by
bridg:Biologic.producingPerformedSubstanceExtraction
none
bridg:Biologic.producingPerformedSubstanceExtraction
producingPerformedSubstanceExtraction
bridg:Performer.performedActivity
performs
bridg:Performer.performedActivity
none
bridg:Performer.performedActivity
performedActivity
bridg:Performer.performedActivity
false
bridg:Performer.performedActivity
Activity
bridg:Performer.performedActivity
urn:CTRRr3:Performer.performed
Activity
bridg:Performer.performedActivity
urn:CTRv1.0:Performer.performed
bridg:Activity.performingPerformer
be performed by
bridg:Activity.performingPerformer
none
bridg:Activity.performingPerformer
performingPerformer
bridg:Performer.performingDevice
be a function performed by
bridg:Performer.performingDevice
none
bridg:Performer.performingDevice
performingDevice
bridg:Performer.performingDevice
false
bridg:Performer.performingDevice
Device
bridg:Performer.performingDevice
urn:CTRRr3:Performer.
Device
bridg:Performer.performingDevice
urn:CTRv1.0:Performer.performing
bridg:Device.performedPerformer
function as
bridg:Device.performedPerformer
none
bridg:Device.performedPerformer
performedPerformer
bridg:Performer.performingOrganization
be a function performed by
bridg:Performer.performingOrganization
none
bridg:Performer.performingOrganization
performingOrganization
bridg:Performer.performingOrganization
false
bridg:Performer.performingOrganization
Organization
bridg:Performer.performingOrganization
urn:CTRRr3:Performer.performing
Organization
bridg:Performer.performingOrganization
urn:CTRv1.0:Performer.performing
bridg:Organization.performedPerformer
function as
bridg:Organization.performedPerformer
none
bridg:Organization.performedPerformer
performedPerformer
bridg:Performer.performingPerson
be a function performed by
bridg:Performer.performingPerson
none
bridg:Performer.performingPerson
performingPerson
bridg:Performer.performingPerson
false
bridg:Performer.performingPerson
Person
bridg:Performer.performingPerson
urn:CTRRr3:Performer.performing
Person
bridg:Performer.performingPerson
urn:CTRv1.0:Performer.performing
bridg:Person.performedPerformer
function as
bridg:Person.performedPerformer
none
bridg:Person.performedPerformer
performedPerformer
bridg:PerformingLaboratory.performingLaboratory
is a function performed by
bridg:PerformingLaboratory.performingLaboratory
none
bridg:PerformingLaboratory.performingLaboratory
performingLaboratory
bridg:PerformingLaboratory.performingLaboratory
false
bridg:PerformingLaboratory.performingLaboratory
Laboratory
bridg:PerformingLaboratory.performingLaboratory
urn:CTRv1.0:PerformingLaboratory.performing
bridg:Laboratory.performedPerformingLaboratory
function as
bridg:Laboratory.performedPerformingLaboratory
none
bridg:Laboratory.performedPerformingLaboratory
performedPerformingLaboratory
bridg:Place.containingPlace
be contained in
bridg:Place.containingPlace
none
bridg:Place.containingPlace
containingPlace
bridg:Place.containingPlace
false
bridg:Place.containingPlace
Place
bridg:Place.containingPlace
urn:CTRv1.0:Place.containing
bridg:Place.containedPlace
contain
bridg:Place.containedPlace
none
bridg:Place.containedPlace
containedPlace
bridg:Place.locatedRegulatoryAuthority
be the location for
bridg:Place.locatedRegulatoryAuthority
none
bridg:Place.locatedRegulatoryAuthority
locatedRegulatoryAuthority
bridg:Place.locatedRegulatoryAuthority
false
bridg:Place.locatedRegulatoryAuthority
RegulatoryAuthority
bridg:Place.locatedRegulatoryAuthority
urn:CTRv1.0:Place.located
bridg:RegulatoryAuthority.locatingPlace
have jurisdiction over
bridg:RegulatoryAuthority.locatingPlace
none
bridg:RegulatoryAuthority.locatingPlace
locatingPlace
bridg:PlannedActivity.containingEpoch
occur in
bridg:PlannedActivity.containingEpoch
none
bridg:PlannedActivity.containingEpoch
containingEpoch
bridg:PlannedActivity.containingEpoch
false
bridg:PlannedActivity.containingEpoch
PerformedActivity
bridg:PlannedActivity.containingEpoch
urn:CTRPv3.8:Epoch.
Epoch
bridg:PlannedActivity.containingEpoch
urn:CTRv1.0:PlannedActivity.containing
bridg:Epoch.containedPlannedActivity
contain
bridg:Epoch.containedPlannedActivity
none
bridg:Epoch.containedPlannedActivity
containedPlannedActivity
bridg:PlannedActivity.locatingServiceDeliveryLocation
take place in
bridg:PlannedActivity.locatingServiceDeliveryLocation
none
bridg:PlannedActivity.locatingServiceDeliveryLocation
locatingServiceDeliveryLocation
bridg:PlannedActivity.locatingServiceDeliveryLocation
false
bridg:PlannedActivity.locatingServiceDeliveryLocation
bridg:ServiceDeliveryLocation.locatedPlannedActivity
be the location for
bridg:ServiceDeliveryLocation.locatedPlannedActivity
none
bridg:ServiceDeliveryLocation.locatedPlannedActivity
locatedPlannedActivity
bridg:PlannedActivity.usedStudyActivity
is a use of
bridg:PlannedActivity.usedStudyActivity
none
bridg:PlannedActivity.usedStudyActivity
usedStudyActivity
bridg:PlannedActivity.usedStudyActivity
false
bridg:PlannedActivity.usedStudyActivity
StudyActivity
bridg:PlannedActivity.usedStudyActivity
urn:CTRv1.0:PlannedActivity.used
bridg:PlannedActivity.usedStudyActivity
urn:HL7SD:PlannedStudy.Precondition1
bridg:StudyActivity.usingPlannedActivity
be used as
bridg:StudyActivity.usingPlannedActivity
none
bridg:StudyActivity.usingPlannedActivity
usingPlannedActivity
bridg:PlannedCompositionRelationship.componentPlannedActivity
is the parent of
bridg:PlannedCompositionRelationship.componentPlannedActivity
none
bridg:PlannedCompositionRelationship.componentPlannedActivity
componentPlannedActivity
bridg:PlannedCompositionRelationship.componentPlannedActivity
false
bridg:PlannedCompositionRelationship.componentPlannedActivity
PlannedActivity
bridg:PlannedCompositionRelationship.componentPlannedActivity
urn:CTRv1.0:PlannedCompositionRelationship.component
bridg:PlannedActivity.compositePlannedCompositionRelationship
be the component of
bridg:PlannedActivity.compositePlannedCompositionRelationship
none
bridg:PlannedActivity.compositePlannedCompositionRelationship
compositePlannedCompositionRelationship
bridg:PlannedCompositionRelationship.compositePlannedActivity
is the component of
bridg:PlannedCompositionRelationship.compositePlannedActivity
none
bridg:PlannedCompositionRelationship.compositePlannedActivity
compositePlannedActivity
bridg:PlannedCompositionRelationship.compositePlannedActivity
false
bridg:PlannedCompositionRelationship.compositePlannedActivity
PlannedActivity
bridg:PlannedCompositionRelationship.compositePlannedActivity
urn:CTRv1.0:PlannedCompositionRelationship.composite
bridg:PlannedActivity.componentPlannedCompositionRelationship
be the parent of
bridg:PlannedActivity.componentPlannedCompositionRelationship
none
bridg:PlannedActivity.componentPlannedCompositionRelationship
componentPlannedCompositionRelationship
bridg:PlannedContingentOnRelationship.contingentPlannedActivity
is a condition for
bridg:PlannedContingentOnRelationship.contingentPlannedActivity
none
bridg:PlannedContingentOnRelationship.contingentPlannedActivity
contingentPlannedActivity
bridg:PlannedContingentOnRelationship.contingentPlannedActivity
false
bridg:PlannedContingentOnRelationship.contingentPlannedActivity
PlannedActivity
bridg:PlannedContingentOnRelationship.contingentPlannedActivity
urn:CTRv1.0:PlannedContingentOnRelationship.contingent
bridg:PlannedActivity.prerequisitePlannedContingentOnRelationship
be contingent upon
bridg:PlannedActivity.prerequisitePlannedContingentOnRelationship
none
bridg:PlannedActivity.prerequisitePlannedContingentOnRelationship
prerequisitePlannedContingentOnRelationship
bridg:PlannedContingentOnRelationship.prerequisiteDefinedObservationResult
be contingent upon
bridg:PlannedContingentOnRelationship.prerequisiteDefinedObservationResult
none
bridg:PlannedContingentOnRelationship.prerequisiteDefinedObservationResult
prerequisiteDefinedObservationResult
bridg:PlannedContingentOnRelationship.prerequisiteDefinedObservationResult
false
bridg:PlannedContingentOnRelationship.prerequisiteDefinedObservationResult
DefinedObservationResult
bridg:PlannedContingentOnRelationship.prerequisiteDefinedObservationResult
urn:CTRv1.0:PlannedContingentOnRelationship.prerequisite
bridg:DefinedObservationResult.contingentPlannedContingentOnRelationship
be a condition for
bridg:DefinedObservationResult.contingentPlannedContingentOnRelationship
none
bridg:DefinedObservationResult.contingentPlannedContingentOnRelationship
contingentPlannedContingentOnRelationship
bridg:PlannedContingentOnRelationship.prerequisitePlannedActivity
be contingent upon
bridg:PlannedContingentOnRelationship.prerequisitePlannedActivity
none
bridg:PlannedContingentOnRelationship.prerequisitePlannedActivity
prerequisitePlannedActivity
bridg:PlannedContingentOnRelationship.prerequisitePlannedActivity
false
bridg:PlannedContingentOnRelationship.prerequisitePlannedActivity
PlannedActivity
bridg:PlannedContingentOnRelationship.prerequisitePlannedActivity
urn:CTRv1.0:PlannedContingentOnRelationship.prerequisite
bridg:PlannedActivity.contingentPlannedContingentOnRelationship
be a condition for
bridg:PlannedActivity.contingentPlannedContingentOnRelationship
none
bridg:PlannedActivity.contingentPlannedContingentOnRelationship
contingentPlannedContingentOnRelationship
bridg:PlannedContingentOnRelationship.prerequisitePlannedCriterionGroup
be contingent upon
bridg:PlannedContingentOnRelationship.prerequisitePlannedCriterionGroup
none
bridg:PlannedContingentOnRelationship.prerequisitePlannedCriterionGroup
prerequisitePlannedCriterionGroup
bridg:PlannedContingentOnRelationship.prerequisitePlannedCriterionGroup
false
bridg:PlannedContingentOnRelationship.prerequisitePlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedContingentOnRelationship.prerequisitePlannedCriterionGroup
urn:CTRv1.0:PlannedContingentOnRelationship.prerequisite
bridg:PlannedCriterionGroup.contingentPlannedContingentOnRelationship
be a condition for
bridg:PlannedCriterionGroup.contingentPlannedContingentOnRelationship
none
bridg:PlannedCriterionGroup.contingentPlannedContingentOnRelationship
contingentPlannedContingentOnRelationship
bridg:PlannedCriterionGroupCompositionRelationship.componentDefinedObservationResult
be the parent of
bridg:PlannedCriterionGroupCompositionRelationship.componentDefinedObservationResult
none
bridg:PlannedCriterionGroupCompositionRelationship.componentDefinedObservationResult
componentDefinedObservationResult
bridg:PlannedCriterionGroupCompositionRelationship.componentDefinedObservationResult
false
bridg:PlannedCriterionGroupCompositionRelationship.componentDefinedObservationResult
DefinedObservationResult
bridg:PlannedCriterionGroupCompositionRelationship.componentDefinedObservationResult
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship.component
bridg:DefinedObservationResult.compositePlannedCriterionGroupCompositionRelationship
be the component of
bridg:DefinedObservationResult.compositePlannedCriterionGroupCompositionRelationship
none
bridg:DefinedObservationResult.compositePlannedCriterionGroupCompositionRelationship
compositePlannedCriterionGroupCompositionRelationship
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedActivity
be the parent of
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedActivity
none
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedActivity
componentPlannedActivity
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedActivity
false
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedActivity
PlannedActivity
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedActivity
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship.component
bridg:PlannedActivity.compositePlannedCriterionGroupCompositionRelationship
be the component of
bridg:PlannedActivity.compositePlannedCriterionGroupCompositionRelationship
none
bridg:PlannedActivity.compositePlannedCriterionGroupCompositionRelationship
compositePlannedCriterionGroupCompositionRelationship
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedCriterionGroup
be the parent of
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedCriterionGroup
none
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedCriterionGroup
componentPlannedCriterionGroup
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedCriterionGroup
false
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedCriterionGroupCompositionRelationship.componentPlannedCriterionGroup
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship.component
bridg:PlannedCriterionGroup.compositePlannedCriterionGroupCompositionRelationship
be the component of
bridg:PlannedCriterionGroup.compositePlannedCriterionGroupCompositionRelationship
none
bridg:PlannedCriterionGroup.compositePlannedCriterionGroupCompositionRelationship
compositePlannedCriterionGroupCompositionRelationship
bridg:PlannedCriterionGroupCompositionRelationship.compositePlannedCriterionGroup
is the component of
bridg:PlannedCriterionGroupCompositionRelationship.compositePlannedCriterionGroup
none
bridg:PlannedCriterionGroupCompositionRelationship.compositePlannedCriterionGroup
compositePlannedCriterionGroup
bridg:PlannedCriterionGroupCompositionRelationship.compositePlannedCriterionGroup
false
bridg:PlannedCriterionGroupCompositionRelationship.compositePlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedCriterionGroupCompositionRelationship.compositePlannedCriterionGroup
urn:CTRv1.0:PlannedCriterionGroupCompositionRelationship.composite
bridg:PlannedCriterionGroup.componentPlannedCriterionGroupCompositionRelationship
be the parent of
bridg:PlannedCriterionGroup.componentPlannedCriterionGroupCompositionRelationship
none
bridg:PlannedCriterionGroup.componentPlannedCriterionGroupCompositionRelationship
componentPlannedCriterionGroupCompositionRelationship
bridg:PlannedCriterionGroupOptionRelationship.choicePlannedCriterionGroup
is an option that can satisfy
bridg:PlannedCriterionGroupOptionRelationship.choicePlannedCriterionGroup
none
bridg:PlannedCriterionGroupOptionRelationship.choicePlannedCriterionGroup
choicePlannedCriterionGroup
bridg:PlannedCriterionGroupOptionRelationship.choicePlannedCriterionGroup
false
bridg:PlannedCriterionGroupOptionRelationship.choicePlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedCriterionGroupOptionRelationship.choicePlannedCriterionGroup
urn:CTRv1.0:PlannedCriterionGroupOptionRelationship.choice
bridg:PlannedCriterionGroup.optionPlannedCriterionGroupOptionRelationship
be a choice that has as option
bridg:PlannedCriterionGroup.optionPlannedCriterionGroupOptionRelationship
none
bridg:PlannedCriterionGroup.optionPlannedCriterionGroupOptionRelationship
optionPlannedCriterionGroupOptionRelationship
bridg:PlannedCriterionGroupOptionRelationship.optionDefinedObservationResult
be a choice that has as option
bridg:PlannedCriterionGroupOptionRelationship.optionDefinedObservationResult
none
bridg:PlannedCriterionGroupOptionRelationship.optionDefinedObservationResult
optionDefinedObservationResult
bridg:PlannedCriterionGroupOptionRelationship.optionDefinedObservationResult
false
bridg:PlannedCriterionGroupOptionRelationship.optionDefinedObservationResult
DefinedObservationResult
bridg:PlannedCriterionGroupOptionRelationship.optionDefinedObservationResult
urn:CTRv1.0:PlannedCriterionGroupOptionRelationship.option
bridg:DefinedObservationResult.choicePlannedCriterionGroupOptionRelationship
be an option that can satisfy
bridg:DefinedObservationResult.choicePlannedCriterionGroupOptionRelationship
none
bridg:DefinedObservationResult.choicePlannedCriterionGroupOptionRelationship
choicePlannedCriterionGroupOptionRelationship
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedActivity
be a choice that has as option
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedActivity
none
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedActivity
optionPlannedActivity
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedActivity
false
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedActivity
PlannedActivity
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedActivity
urn:CTRv1.0:PlannedCriterionGroupOptionRelationship.option
bridg:PlannedActivity.choicePlannedCriterionGroupOptionRelationship
be an option that can satisfy
bridg:PlannedActivity.choicePlannedCriterionGroupOptionRelationship
none
bridg:PlannedActivity.choicePlannedCriterionGroupOptionRelationship
choicePlannedCriterionGroupOptionRelationship
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedCriterionGroup
be a choice that has as option
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedCriterionGroup
none
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedCriterionGroup
optionPlannedCriterionGroup
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedCriterionGroup
false
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedCriterionGroupOptionRelationship.optionPlannedCriterionGroup
urn:CTRv1.0:PlannedCriterionGroupOptionRelationship.option
bridg:PlannedCriterionGroup.choicePlannedCriterionGroupOptionRelationship
be an option that can satisfy
bridg:PlannedCriterionGroup.choicePlannedCriterionGroupOptionRelationship
none
bridg:PlannedCriterionGroup.choicePlannedCriterionGroupOptionRelationship
choicePlannedCriterionGroupOptionRelationship
bridg:PlannedEligibilityCriterion.requiredDefinedEligibilityCriterionAnswer
requires for eligibility
bridg:PlannedEligibilityCriterion.requiredDefinedEligibilityCriterionAnswer
none
bridg:PlannedEligibilityCriterion.requiredDefinedEligibilityCriterionAnswer
requiredDefinedEligibilityCriterionAnswer
bridg:PlannedEligibilityCriterion.requiredDefinedEligibilityCriterionAnswer
false
bridg:PlannedEligibilityCriterion.requiredDefinedEligibilityCriterionAnswer
bridg:DefinedEligibilityCriterionAnswer.requiringPlannedEligibilityCriterion
be required for eligibility for
bridg:DefinedEligibilityCriterionAnswer.requiringPlannedEligibilityCriterion
none
bridg:DefinedEligibilityCriterionAnswer.requiringPlannedEligibilityCriterion
requiringPlannedEligibilityCriterion
bridg:PlannedOptionRelationship.choicePlannedActivity
is an option that can satisfy
bridg:PlannedOptionRelationship.choicePlannedActivity
none
bridg:PlannedOptionRelationship.choicePlannedActivity
choicePlannedActivity
bridg:PlannedOptionRelationship.choicePlannedActivity
false
bridg:PlannedOptionRelationship.choicePlannedActivity
PlannedActivity
bridg:PlannedOptionRelationship.choicePlannedActivity
urn:CTRv1.0:PlannedOptionRelationship.choice
bridg:PlannedActivity.optionPlannedOptionRelationship
be a choice that has as option
bridg:PlannedActivity.optionPlannedOptionRelationship
none
bridg:PlannedActivity.optionPlannedOptionRelationship
optionPlannedOptionRelationship
bridg:PlannedOptionRelationship.optionPlannedActivity
is a choice that has as option
bridg:PlannedOptionRelationship.optionPlannedActivity
none
bridg:PlannedOptionRelationship.optionPlannedActivity
optionPlannedActivity
bridg:PlannedOptionRelationship.optionPlannedActivity
false
bridg:PlannedOptionRelationship.optionPlannedActivity
PlannedActivity
bridg:PlannedOptionRelationship.optionPlannedActivity
urn:CTRv1.0:PlannedOptionRelationship.option
bridg:PlannedActivity.choicePlannedOptionRelationship
be an option that can satisfy
bridg:PlannedActivity.choicePlannedOptionRelationship
none
bridg:PlannedActivity.choicePlannedOptionRelationship
choicePlannedOptionRelationship
bridg:PlannedRepeatActivityUntilRule.repeatedPlannedActivity
triggers the cessation of
bridg:PlannedRepeatActivityUntilRule.repeatedPlannedActivity
none
bridg:PlannedRepeatActivityUntilRule.repeatedPlannedActivity
repeatedPlannedActivity
bridg:PlannedRepeatActivityUntilRule.repeatedPlannedActivity
false
bridg:PlannedRepeatActivityUntilRule.repeatedPlannedActivity
PlannedActivity
bridg:PlannedRepeatActivityUntilRule.repeatedPlannedActivity
urn:CTRv1.0:PlannedRepeatActivityUntilRule.repeated
bridg:PlannedActivity.triggeringPlannedRepeatActivityUntilRule
be repeated until
bridg:PlannedActivity.triggeringPlannedRepeatActivityUntilRule
none
bridg:PlannedActivity.triggeringPlannedRepeatActivityUntilRule
triggeringPlannedRepeatActivityUntilRule
bridg:PlannedRepeatActivityUntilRule.triggeringDefinedObservationResult
be repeated until
bridg:PlannedRepeatActivityUntilRule.triggeringDefinedObservationResult
none
bridg:PlannedRepeatActivityUntilRule.triggeringDefinedObservationResult
triggeringDefinedObservationResult
bridg:PlannedRepeatActivityUntilRule.triggeringDefinedObservationResult
false
bridg:PlannedRepeatActivityUntilRule.triggeringDefinedObservationResult
DefinedObservationResult
bridg:PlannedRepeatActivityUntilRule.triggeringDefinedObservationResult
urn:CTRv1.0:PlannedRepeatActivityUntilRule.triggering
bridg:DefinedObservationResult.repeatedPlannedRepeatActivityUntilRule
trigger the cessation of
bridg:DefinedObservationResult.repeatedPlannedRepeatActivityUntilRule
none
bridg:DefinedObservationResult.repeatedPlannedRepeatActivityUntilRule
repeatedPlannedRepeatActivityUntilRule
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedActivity
be repeated until
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedActivity
none
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedActivity
triggeringPlannedActivity
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedActivity
false
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedActivity
PlannedActivity
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedActivity
urn:CTRv1.0:PlannedRepeatActivityUntilRule.triggering
bridg:PlannedActivity.repeatedPlannedRepeatActivityUntilRule
trigger the cessation of
bridg:PlannedActivity.repeatedPlannedRepeatActivityUntilRule
none
bridg:PlannedActivity.repeatedPlannedRepeatActivityUntilRule
repeatedPlannedRepeatActivityUntilRule
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedCriterionGroup
be repeated until
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedCriterionGroup
none
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedCriterionGroup
triggeringPlannedCriterionGroup
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedCriterionGroup
false
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedCriterionGroup
PlannedCriterionGroup
bridg:PlannedRepeatActivityUntilRule.triggeringPlannedCriterionGroup
urn:CTRv1.0:PlannedRepeatActivityUntilRule.triggering
bridg:PlannedCriterionGroup.repeatedPlannedRepeatActivityUntilRule
trigger the cessation of
bridg:PlannedCriterionGroup.repeatedPlannedRepeatActivityUntilRule
none
bridg:PlannedCriterionGroup.repeatedPlannedRepeatActivityUntilRule
repeatedPlannedRepeatActivityUntilRule
bridg:PlannedStudySite.executesStudyProtocolVersion
plans to execute
bridg:PlannedStudySite.executesStudyProtocolVersion
none
bridg:PlannedStudySite.executesStudyProtocolVersion
executesStudyProtocolVersion
bridg:PlannedStudySite.executesStudyProtocolVersion
false
bridg:PlannedStudySite.executesStudyProtocolVersion
StudyProtocolVersion
bridg:PlannedStudySite.executesStudyProtocolVersion
urn:CTRv1.0:PlannedStudySite.executes
bridg:StudyProtocolVersion.executingPlannedStudySite
be planned to be executed at
bridg:StudyProtocolVersion.executingPlannedStudySite
none
bridg:StudyProtocolVersion.executingPlannedStudySite
executingPlannedStudySite
bridg:PlannedStudySite.performingHealthcareFacility
be a function planned to be performed by
bridg:PlannedStudySite.performingHealthcareFacility
none
bridg:PlannedStudySite.performingHealthcareFacility
performingHealthcareFacility
bridg:PlannedStudySite.performingHealthcareFacility
false
bridg:PlannedStudySite.performingHealthcareFacility
HealthcareFacility
bridg:PlannedStudySite.performingHealthcareFacility
urn:CTRv1.0:PlannedStudySite.performing
bridg:HealthcareFacility.performedPlannedStudySite
plan to function as
bridg:HealthcareFacility.performedPlannedStudySite
none
bridg:HealthcareFacility.performedPlannedStudySite
performedPlannedStudySite
bridg:PlannedStudySite.performingOrganization
be a function planned to be performed by
bridg:PlannedStudySite.performingOrganization
none
bridg:PlannedStudySite.performingOrganization
performingOrganization
bridg:PlannedStudySite.performingOrganization
false
bridg:PlannedStudySite.performingOrganization
Organization
bridg:PlannedStudySite.performingOrganization
urn:CTRv1.0:PlannedStudySite.performing
bridg:Organization.performedPlannedStudySite
plan to function as
bridg:Organization.performedPlannedStudySite
none
bridg:Organization.performedPlannedStudySite
performedPlannedStudySite
bridg:PlannedStudySubject.constrainingDefinedEligibilityCriterion
be constrained by
bridg:PlannedStudySubject.constrainingDefinedEligibilityCriterion
none
bridg:PlannedStudySubject.constrainingDefinedEligibilityCriterion
constrainingDefinedEligibilityCriterion
bridg:PlannedStudySubject.constrainingDefinedEligibilityCriterion
false
bridg:PlannedStudySubject.constrainingDefinedEligibilityCriterion
Indicates the criteria a particular PlannedStudySubject is expected to adhere to.
bridg:DefinedEligibilityCriterion.constrainedPlannedStudySubject
constrain
bridg:DefinedEligibilityCriterion.constrainedPlannedStudySubject
none
bridg:DefinedEligibilityCriterion.constrainedPlannedStudySubject
constrainedPlannedStudySubject
bridg:PlannedStudySubject.plannedForStudyProtocolVersion
participates in
bridg:PlannedStudySubject.plannedForStudyProtocolVersion
none
bridg:PlannedStudySubject.plannedForStudyProtocolVersion
plannedForStudyProtocolVersion
bridg:PlannedStudySubject.plannedForStudyProtocolVersion
false
bridg:PlannedStudySubject.plannedForStudyProtocolVersion
Indicates the types of StudySubjects intended to participate in the StudyProtocolVersion.
bridg:PlannedStudySubject.plannedForStudyProtocolVersion
ActualIndicator should be set to 'false' for the Entity that is the subject
bridg:StudyProtocolVersion.intendedPlannedStudySubject
is participated in by
bridg:StudyProtocolVersion.intendedPlannedStudySubject
none
bridg:StudyProtocolVersion.intendedPlannedStudySubject
intendedPlannedStudySubject
bridg:ProcessedProduct.producedProduct
produces
bridg:ProcessedProduct.producedProduct
none
bridg:ProcessedProduct.producedProduct
producedProduct
bridg:ProcessedProduct.producedProduct
false
bridg:ProcessedProduct.producedProduct
Product
bridg:ProcessedProduct.producedProduct
urn:CTRv1.0:ProcessedProduct.produced
bridg:Product.producingProcessedProduct
be produced by
bridg:Product.producingProcessedProduct
none
bridg:Product.producingProcessedProduct
producingProcessedProduct
bridg:ProcessedProduct.producingProcessor
is produced by
bridg:ProcessedProduct.producingProcessor
none
bridg:ProcessedProduct.producingProcessor
producingProcessor
bridg:ProcessedProduct.producingProcessor
false
bridg:ProcessedProduct.producingProcessor
Processor
bridg:ProcessedProduct.producingProcessor
urn:CTRv1.0:ProcessedProduct.producing
bridg:Processor.producedProcessedProduct
produces
bridg:Processor.producedProcessedProduct
none
bridg:Processor.producedProcessedProduct
producedProcessedProduct
bridg:ProcessingSite.fabricatingProduct
fabricates
bridg:ProcessingSite.fabricatingProduct
none
bridg:ProcessingSite.fabricatingProduct
fabricatingProduct
bridg:ProcessingSite.fabricatingProduct
false
bridg:ProcessingSite.fabricatingProduct
bridg:Product.fabricatedProcessingSite
be fabricated by
bridg:Product.fabricatedProcessingSite
none
bridg:Product.fabricatedProcessingSite
fabricatedProcessingSite
bridg:ProcessingSite.operatingProcessor
manufactures for
bridg:ProcessingSite.operatingProcessor
none
bridg:ProcessingSite.operatingProcessor
operatingProcessor
bridg:ProcessingSite.operatingProcessor
false
bridg:ProcessingSite.operatingProcessor
bridg:Processor.operatedProcessingSite
manufacture at
bridg:Processor.operatedProcessingSite
none
bridg:Processor.operatedProcessingSite
operatedProcessingSite
bridg:ProcessingSite.performingPlace
is a function performed by
bridg:ProcessingSite.performingPlace
none
bridg:ProcessingSite.performingPlace
performingPlace
bridg:ProcessingSite.performingPlace
false
bridg:ProcessingSite.performingPlace
bridg:Place.performedProcessingSite
function as
bridg:Place.performedProcessingSite
none
bridg:Place.performedProcessingSite
performedProcessingSite
bridg:Processor.performingOrganization
is a function performed by
bridg:Processor.performingOrganization
none
bridg:Processor.performingOrganization
performingOrganization
bridg:Processor.performingOrganization
false
bridg:Processor.performingOrganization
Organization
bridg:Processor.performingOrganization
urn:CTRv1.0:Processor.performing
bridg:Organization.performedProcessor
function as
bridg:Organization.performedProcessor
none
bridg:Organization.performedProcessor
performedProcessor
bridg:ProductGroup.groupedProduct
groups
bridg:ProductGroup.groupedProduct
shared
bridg:ProductGroup.groupedProduct
groupedProduct
bridg:ProductGroup.groupedProduct
false
bridg:ProductGroup.groupedProduct
bridg:Product.groupingProductGroup
be grouped by
bridg:Product.groupingProductGroup
shared
bridg:Product.groupingProductGroup
groupingProductGroup
bridg:ProductRelationship.sourceProduct
has as source
bridg:ProductRelationship.sourceProduct
none
bridg:ProductRelationship.sourceProduct
sourceProduct
bridg:ProductRelationship.sourceProduct
false
bridg:ProductRelationship.sourceProduct
Product
bridg:ProductRelationship.sourceProduct
urn:CTRRr3:ProductPart.composite
Product
bridg:ProductRelationship.sourceProduct
urn:CTRv1.0:ProductRelationship.source
bridg:Product.targetProductRelationship
be the source for
bridg:Product.targetProductRelationship
none
bridg:Product.targetProductRelationship
targetProductRelationship
bridg:ProductRelationship.targetProduct
has as target
bridg:ProductRelationship.targetProduct
none
bridg:ProductRelationship.targetProduct
targetProduct
bridg:ProductRelationship.targetProduct
false
bridg:ProductRelationship.targetProduct
Product
bridg:ProductRelationship.targetProduct
urn:CTRRr3:ProductPart.performing
Product
bridg:ProductRelationship.targetProduct
urn:CTRv1.0:ProductRelationship.target
bridg:Product.sourceProductRelationship
be the target for
bridg:Product.sourceProductRelationship
none
bridg:Product.sourceProductRelationship
sourceProductRelationship
bridg:QualifiedPerson.credentialingOrganization
is credentialed by
bridg:QualifiedPerson.credentialingOrganization
none
bridg:QualifiedPerson.credentialingOrganization
credentialingOrganization
bridg:QualifiedPerson.credentialingOrganization
false
bridg:QualifiedPerson.credentialingOrganization
Organization
bridg:QualifiedPerson.credentialingOrganization
urn:CTRv1.0:QualifiedPerson.credentialing
bridg:Organization.credentialedQualifiedPerson
credential
bridg:Organization.credentialedQualifiedPerson
none
bridg:Organization.credentialedQualifiedPerson
credentialedQualifiedPerson
bridg:QualifiedPerson.locatingPlace
be qualified in
bridg:QualifiedPerson.locatingPlace
none
bridg:QualifiedPerson.locatingPlace
locatingPlace
bridg:QualifiedPerson.locatingPlace
false
bridg:QualifiedPerson.locatingPlace
Place
bridg:QualifiedPerson.locatingPlace
urn:CTRv1.0:QualifiedPerson.locating
bridg:Place.locatedQualifiedPerson
be the location in which the qualification is granted for
bridg:Place.locatedQualifiedPerson
none
bridg:Place.locatedQualifiedPerson
locatedQualifiedPerson
bridg:QualifiedPerson.performingPerson
is a function performed by
bridg:QualifiedPerson.performingPerson
none
bridg:QualifiedPerson.performingPerson
performingPerson
bridg:QualifiedPerson.performingPerson
false
bridg:QualifiedPerson.performingPerson
Person
bridg:QualifiedPerson.performingPerson
urn:CTRv1.0:QualifiedPerson.performing
bridg:Person.performedQualifiedPerson
function as
bridg:Person.performedQualifiedPerson
none
bridg:Person.performedQualifiedPerson
performedQualifiedPerson
bridg:RandomizationBookEntry.definingPlannedRandomizationBookAllocation
is defined by
bridg:RandomizationBookEntry.definingPlannedRandomizationBookAllocation
none
bridg:RandomizationBookEntry.definingPlannedRandomizationBookAllocation
definingPlannedRandomizationBookAllocation
bridg:RandomizationBookEntry.definingPlannedRandomizationBookAllocation
false
bridg:RandomizationBookEntry.definingPlannedRandomizationBookAllocation
PlannedRandomizationBookAllocation
bridg:RandomizationBookEntry.definingPlannedRandomizationBookAllocation
urn:CTRRr3:RandomizationBookEntry.defining
bridg:PlannedRandomizationBookAllocation.definedRandomizationBookEntry
defines
bridg:PlannedRandomizationBookAllocation.definedRandomizationBookEntry
none
bridg:PlannedRandomizationBookAllocation.definedRandomizationBookEntry
definedRandomizationBookEntry
bridg:RandomizationBookEntry.randomizedStratumGroup
randomize
bridg:RandomizationBookEntry.randomizedStratumGroup
none
bridg:RandomizationBookEntry.randomizedStratumGroup
randomizedStratumGroup
bridg:RandomizationBookEntry.randomizedStratumGroup
false
bridg:RandomizationBookEntry.randomizedStratumGroup
StratumGroup
bridg:RandomizationBookEntry.randomizedStratumGroup
urn:CTRRr3:RandomizationBookEntry.randomized
bridg:StratumGroup.randomizingRandomizationBookEntry
be randomized by
bridg:StratumGroup.randomizingRandomizationBookEntry
none
bridg:StratumGroup.randomizingRandomizationBookEntry
randomizingRandomizationBookEntry
bridg:ReferenceResult.performingDevice
apply to results produced by
bridg:ReferenceResult.performingDevice
none
bridg:ReferenceResult.performingDevice
performingDevice
bridg:ReferenceResult.performingDevice
false
bridg:ReferenceResult.performingDevice
Device
bridg:ReferenceResult.performingDevice
urn:CTRv1.0:ReferenceResult.performing
bridg:Device.performedReferenceResult
produce
bridg:Device.performedReferenceResult
none
bridg:Device.performedReferenceResult
performedReferenceResult
bridg:ReferenceResult.performingPerformingLaboratory
apply to results produced by
bridg:ReferenceResult.performingPerformingLaboratory
none
bridg:ReferenceResult.performingPerformingLaboratory
performingPerformingLaboratory
bridg:ReferenceResult.performingPerformingLaboratory
false
bridg:ReferenceResult.performingPerformingLaboratory
PerformingLaboratory
bridg:ReferenceResult.performingPerformingLaboratory
urn:CTRv1.0:ReferenceResult.performing
bridg:PerformingLaboratory.performedReferenceResult
produce
bridg:PerformingLaboratory.performedReferenceResult
none
bridg:PerformingLaboratory.performedReferenceResult
performedReferenceResult
bridg:ReferenceToStudyResults.referencedStudyExecution
references the results of
bridg:ReferenceToStudyResults.referencedStudyExecution
none
bridg:ReferenceToStudyResults.referencedStudyExecution
referencedStudyExecution
bridg:ReferenceToStudyResults.referencedStudyExecution
false
bridg:ReferenceToStudyResults.referencedStudyExecution
bridg:ReferenceToStudyResults.referencedStudyExecution
urn:CTRRr3:StudyReference.referringStudyRelatedIndicator
StudyExecution
bridg:ReferenceToStudyResults.referencedStudyExecution
urn:CTRv1.0:ReferenceToStudyResults.referenced
bridg:StudyExecution.referencingReferenceToStudyResults
have results referenced in
bridg:StudyExecution.referencingReferenceToStudyResults
none
bridg:StudyExecution.referencingReferenceToStudyResults
referencingReferenceToStudyResults
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
be a function performed by
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
none
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
performingHealthcareProvider
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
false
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
HealthcareProvider
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
urn:CTRRr3:RegulatoryApplicationSponsor.performing
HealthcareProvider
bridg:RegulatoryApplicationSponsor.performingHealthcareProvider
urn:CTRv1.0:RegulatoryApplicationSponsor.performing
bridg:HealthcareProvider.performedRegulatoryApplicationSponsor
function as
bridg:HealthcareProvider.performedRegulatoryApplicationSponsor
none
bridg:HealthcareProvider.performedRegulatoryApplicationSponsor
performedRegulatoryApplicationSponsor
bridg:RegulatoryApplicationSponsor.performingOrganization
be a function performed by
bridg:RegulatoryApplicationSponsor.performingOrganization
none
bridg:RegulatoryApplicationSponsor.performingOrganization
performingOrganization
bridg:RegulatoryApplicationSponsor.performingOrganization
false
bridg:RegulatoryApplicationSponsor.performingOrganization
Organization
bridg:RegulatoryApplicationSponsor.performingOrganization
urn:CTRRr3:RegulatoryApplicationSponsor.performing
Organization
bridg:RegulatoryApplicationSponsor.performingOrganization
urn:CTRv1.0:RegulatoryApplicationSponsor.performing
bridg:Organization.performedRegulatoryApplicationSponsor
function as
bridg:Organization.performedRegulatoryApplicationSponsor
none
bridg:Organization.performedRegulatoryApplicationSponsor
performedRegulatoryApplicationSponsor
bridg:RegulatoryAssessment.performingRegulatoryAuthority
is performed by
bridg:RegulatoryAssessment.performingRegulatoryAuthority
none
bridg:RegulatoryAssessment.performingRegulatoryAuthority
performingRegulatoryAuthority
bridg:RegulatoryAssessment.performingRegulatoryAuthority
false
bridg:RegulatoryAssessment.performingRegulatoryAuthority
RegulatoryAuthority
bridg:RegulatoryAssessment.performingRegulatoryAuthority
urn:CTRRr3:RegulatoryAssessment.performing
RegulatoryAuthority
bridg:RegulatoryAssessment.performingRegulatoryAuthority
urn:CTRv1.0:RegulatoryAssessment.performing
bridg:RegulatoryAuthority.performedRegulatoryAssessment
perform
bridg:RegulatoryAuthority.performedRegulatoryAssessment
none
bridg:RegulatoryAuthority.performedRegulatoryAssessment
performedRegulatoryAssessment
bridg:RelevantRegulation.governedInterventionalStudyProtocolVersion
governs
bridg:RelevantRegulation.governedInterventionalStudyProtocolVersion
none
bridg:RelevantRegulation.governedInterventionalStudyProtocolVersion
governedInterventionalStudyProtocolVersion
bridg:RelevantRegulation.governedInterventionalStudyProtocolVersion
false
bridg:RelevantRegulation.governedInterventionalStudyProtocolVersion
bridg:InterventionalStudyProtocolVersion.governingRelevantRegulation
be governed by
bridg:InterventionalStudyProtocolVersion.governingRelevantRegulation
none
bridg:InterventionalStudyProtocolVersion.governingRelevantRegulation
governingRelevantRegulation
bridg:ReportReceiver.performingOrganization
be a function performed by
bridg:ReportReceiver.performingOrganization
none
bridg:ReportReceiver.performingOrganization
performingOrganization
bridg:ReportReceiver.performingOrganization
false
bridg:ReportReceiver.performingOrganization
Organization
bridg:ReportReceiver.performingOrganization
urn:CTRv1.0:ReportReceiver.performing
bridg:Organization.performedReportReceiver
function as
bridg:Organization.performedReportReceiver
none
bridg:Organization.performedReportReceiver
performedReportReceiver
bridg:ReportReceiver.performingPerson
be a function performed by
bridg:ReportReceiver.performingPerson
none
bridg:ReportReceiver.performingPerson
performingPerson
bridg:ReportReceiver.performingPerson
false
bridg:ReportReceiver.performingPerson
Person
bridg:ReportReceiver.performingPerson
urn:CTRv1.0:ReportReceiver.performing
bridg:Person.performedReportReceiver
function as
bridg:Person.performedReportReceiver
none
bridg:Person.performedReportReceiver
performedReportReceiver
bridg:ReportReceiver.receivedReportVersion
receives
bridg:ReportReceiver.receivedReportVersion
none
bridg:ReportReceiver.receivedReportVersion
receivedReportVersion
bridg:ReportReceiver.receivedReportVersion
false
bridg:ReportReceiver.receivedReportVersion
ReportVersion
bridg:ReportReceiver.receivedReportVersion
urn:CTRv1.0:ReportReceiver.received
bridg:ReportVersion.receivingReportReceiver
be received by
bridg:ReportVersion.receivingReportReceiver
none
bridg:ReportVersion.receivingReportReceiver
receivingReportReceiver
bridg:ReportSubmitter.performingResearchStaff
is a function performed by
bridg:ReportSubmitter.performingResearchStaff
none
bridg:ReportSubmitter.performingResearchStaff
performingResearchStaff
bridg:ReportSubmitter.performingResearchStaff
false
bridg:ReportSubmitter.performingResearchStaff
ResearchStaff
bridg:ReportSubmitter.performingResearchStaff
urn:CTRv1.0:ReportSubmitter.performing
bridg:ResearchStaff.performedReportSubmitter
function as
bridg:ResearchStaff.performedReportSubmitter
none
bridg:ResearchStaff.performedReportSubmitter
performedReportSubmitter
bridg:ReportSubmitter.submittedSafetyReportVersion
submits
bridg:ReportSubmitter.submittedSafetyReportVersion
none
bridg:ReportSubmitter.submittedSafetyReportVersion
submittedSafetyReportVersion
bridg:ReportSubmitter.submittedSafetyReportVersion
false
bridg:ReportSubmitter.submittedSafetyReportVersion
SafetyReportVersion
bridg:ReportSubmitter.submittedSafetyReportVersion
urn:CTRv1.0:ReportSubmitter.submitted
bridg:SafetyReportVersion.submittingReportSubmitter
is submitted by
bridg:SafetyReportVersion.submittingReportSubmitter
none
bridg:SafetyReportVersion.submittingReportSubmitter
submittingReportSubmitter
bridg:ReportVersion.describedPerformedObservationResult
describe
bridg:ReportVersion.describedPerformedObservationResult
none
bridg:ReportVersion.describedPerformedObservationResult
describedPerformedObservationResult
bridg:ReportVersion.describedPerformedObservationResult
false
bridg:ReportVersion.describedPerformedObservationResult
PerformedObservationResult
bridg:ReportVersion.describedPerformedObservationResult
urn:CTRv1.0:ReportVersion.described
bridg:PerformedObservationResult.describingReportVersion
be described by
bridg:PerformedObservationResult.describingReportVersion
none
bridg:PerformedObservationResult.describingReportVersion
describingReportVersion
bridg:ResearchOrganization.performingOrganization
is a function performed by
bridg:ResearchOrganization.performingOrganization
none
bridg:ResearchOrganization.performingOrganization
performingOrganization
bridg:ResearchOrganization.performingOrganization
false
bridg:ResearchOrganization.performingOrganization
bridg:ResearchOrganization.performingOrganization
urn:CTRR:Responsible_Contact_Person
Organization
bridg:ResearchOrganization.performingOrganization
urn:CTRv1.0:ResearchOrganization.performing
bridg:Organization.performedResearchOrganization
function as
bridg:Organization.performedResearchOrganization
none
bridg:Organization.performedResearchOrganization
performedResearchOrganization
bridg:ResearchStaff.performingPerson
is a function performed by
bridg:ResearchStaff.performingPerson
none
bridg:ResearchStaff.performingPerson
performingPerson
bridg:ResearchStaff.performingPerson
false
bridg:ResearchStaff.performingPerson
n:PersonRole
bridg:ResearchStaff.performingPerson
urn:CTRPv3.8:ClinicalResearchStaff.Is_a
Person
bridg:ResearchStaff.performingPerson
urn:CTRv1.0:ResearchStaff.performing
bridg:Person.performedResearchStaff
function as
bridg:Person.performedResearchStaff
none
bridg:Person.performedResearchStaff
performedResearchStaff
bridg:ResearchStaff.staffedResearchOrganization
staffs
bridg:ResearchStaff.staffedResearchOrganization
none
bridg:ResearchStaff.staffedResearchOrganization
staffedResearchOrganization
bridg:ResearchStaff.staffedResearchOrganization
false
bridg:ResearchStaff.staffedResearchOrganization
ResearchOrganization
bridg:ResearchStaff.staffedResearchOrganization
urn:CTRv1.0:ResearchStaff.staffed
bridg:ResearchOrganization.staffingResearchStaff
be staffed by
bridg:ResearchOrganization.staffingResearchStaff
none
bridg:ResearchOrganization.staffingResearchStaff
staffingResearchStaff
bridg:Resource.providingResourceProvider
be provided by
bridg:Resource.providingResourceProvider
none
bridg:Resource.providingResourceProvider
providingResourceProvider
bridg:Resource.providingResourceProvider
false
bridg:Resource.providingResourceProvider
ResourceProvider
bridg:Resource.providingResourceProvider
urn:CTRRr3:Resource.providing
ResourceProvider
bridg:Resource.providingResourceProvider
urn:CTRv1.0:Resource.providing
bridg:ResourceProvider.providedResource
provides
bridg:ResourceProvider.providedResource
none
bridg:ResourceProvider.providedResource
providedResource
bridg:ResourceProvider.performingOrganization
be a function performed by
bridg:ResourceProvider.performingOrganization
none
bridg:ResourceProvider.performingOrganization
performingOrganization
bridg:ResourceProvider.performingOrganization
false
bridg:ResourceProvider.performingOrganization
Organization
bridg:ResourceProvider.performingOrganization
urn:CTRRr3:ResourceProvider.performing
Organization
bridg:ResourceProvider.performingOrganization
urn:CTRv1.0:ResourceProvider.performing
bridg:Organization.performedResourceProvider
function as
bridg:Organization.performedResourceProvider
none
bridg:Organization.performedResourceProvider
performedResourceProvider
bridg:ResourceProvider.performingPerson
be a function performed by
bridg:ResourceProvider.performingPerson
none
bridg:ResourceProvider.performingPerson
performingPerson
bridg:ResourceProvider.performingPerson
false
bridg:ResourceProvider.performingPerson
Person
bridg:ResourceProvider.performingPerson
urn:CTRRr3:ResourceProvider.performing
Person
bridg:ResourceProvider.performingPerson
urn:CTRv1.0:ResourceProvider.performing
bridg:Person.performedResourceProvider
function as
bridg:Person.performedResourceProvider
none
bridg:Person.performedResourceProvider
performedResourceProvider
bridg:ReviewableUnit.groupingSubmission
is grouped into
bridg:ReviewableUnit.groupingSubmission
none
bridg:ReviewableUnit.groupingSubmission
groupingSubmission
bridg:ReviewableUnit.groupingSubmission
false
bridg:ReviewableUnit.groupingSubmission
Submission
bridg:ReviewableUnit.groupingSubmission
urn:CTRv1.0:ReviewableUnit.grouping
bridg:Submission.groupedReviewableUnit
group
bridg:Submission.groupedReviewableUnit
composite
bridg:Submission.groupedReviewableUnit
groupedReviewableUnit
bridg:SafetyReportVersion.describedAdverseEvent
describe
bridg:SafetyReportVersion.describedAdverseEvent
none
bridg:SafetyReportVersion.describedAdverseEvent
describedAdverseEvent
bridg:SafetyReportVersion.describedAdverseEvent
false
bridg:SafetyReportVersion.describedAdverseEvent
AdverseEvent
bridg:SafetyReportVersion.describedAdverseEvent
urn:CTRv1.0:SafetyReportVersion.described
bridg:AdverseEvent.describingSafetyReportVersion
be described by
bridg:AdverseEvent.describingSafetyReportVersion
none
bridg:AdverseEvent.describingSafetyReportVersion
describingSafetyReportVersion
bridg:SafetyReportVersion.describedPerformedProductProblemDiscovery
describe
bridg:SafetyReportVersion.describedPerformedProductProblemDiscovery
none
bridg:SafetyReportVersion.describedPerformedProductProblemDiscovery
describedPerformedProductProblemDiscovery
bridg:SafetyReportVersion.describedPerformedProductProblemDiscovery
false
bridg:SafetyReportVersion.describedPerformedProductProblemDiscovery
PerformedProductProblemDiscovery
bridg:SafetyReportVersion.describedPerformedProductProblemDiscovery
urn:CTRv1.0:SafetyReportVersion.described
bridg:PerformedProductProblemDiscovery.describingSafetyReportVersion
be described by
bridg:PerformedProductProblemDiscovery.describingSafetyReportVersion
none
bridg:PerformedProductProblemDiscovery.describingSafetyReportVersion
describingSafetyReportVersion
bridg:SafetyReportVersion.reportedPerformedProcedure
report as prior therapies
bridg:SafetyReportVersion.reportedPerformedProcedure
none
bridg:SafetyReportVersion.reportedPerformedProcedure
reportedPerformedProcedure
bridg:SafetyReportVersion.reportedPerformedProcedure
false
bridg:SafetyReportVersion.reportedPerformedProcedure
bridg:PerformedProcedure.reportingSafetyReportVersion
be reported as a prior therapy in
bridg:PerformedProcedure.reportingSafetyReportVersion
none
bridg:PerformedProcedure.reportingSafetyReportVersion
reportingSafetyReportVersion
bridg:SampleSizeConsideration.includingStatisticalAnalysisPlanVersion
is included in
bridg:SampleSizeConsideration.includingStatisticalAnalysisPlanVersion
none
bridg:SampleSizeConsideration.includingStatisticalAnalysisPlanVersion
includingStatisticalAnalysisPlanVersion
bridg:SampleSizeConsideration.includingStatisticalAnalysisPlanVersion
false
bridg:SampleSizeConsideration.includingStatisticalAnalysisPlanVersion
Identifies the considerations that inform the calculation of the sample size for a given version of a statistical analysis plan.
StatisticalAnalysisPlanVersion
bridg:SampleSizeConsideration.includingStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:SampleSizeConsideration.
bridg:StatisticalAnalysisPlanVersion.includedSampleSizeConsideration
include
bridg:StatisticalAnalysisPlanVersion.includedSampleSizeConsideration
shared
bridg:StatisticalAnalysisPlanVersion.includedSampleSizeConsideration
includedSampleSizeConsideration
bridg:ScheduledActivity.instantiatedPlannedActivity
instantiates
bridg:ScheduledActivity.instantiatedPlannedActivity
none
bridg:ScheduledActivity.instantiatedPlannedActivity
instantiatedPlannedActivity
bridg:ScheduledActivity.instantiatedPlannedActivity
false
bridg:ScheduledActivity.instantiatedPlannedActivity
bridg:PlannedActivity.instantiatingScheduledActivity
be instantiated by
bridg:PlannedActivity.instantiatingScheduledActivity
none
bridg:PlannedActivity.instantiatingScheduledActivity
instantiatingScheduledActivity
bridg:ServiceDeliveryLocation.locatedOrganization
be delivery location for
bridg:ServiceDeliveryLocation.locatedOrganization
none
bridg:ServiceDeliveryLocation.locatedOrganization
locatedOrganization
bridg:ServiceDeliveryLocation.locatedOrganization
false
bridg:ServiceDeliveryLocation.locatedOrganization
Organization
bridg:ServiceDeliveryLocation.locatedOrganization
urn:CTRv1.0:ServiceDeliveryLocation.located
bridg:Organization.locatingServiceDeliveryLocation
receive delivery at
bridg:Organization.locatingServiceDeliveryLocation
none
bridg:Organization.locatingServiceDeliveryLocation
locatingServiceDeliveryLocation
bridg:ServiceDeliveryLocation.locatedPlace
be located at
bridg:ServiceDeliveryLocation.locatedPlace
none
bridg:ServiceDeliveryLocation.locatedPlace
locatedPlace
bridg:ServiceDeliveryLocation.locatedPlace
false
bridg:ServiceDeliveryLocation.locatedPlace
Place
bridg:ServiceDeliveryLocation.locatedPlace
urn:CTRv1.0:ServiceDeliveryLocation.located
bridg:Place.locatingServiceDeliveryLocation
be the location for
bridg:Place.locatingServiceDeliveryLocation
none
bridg:Place.locatingServiceDeliveryLocation
locatingServiceDeliveryLocation
bridg:Specimen.performingMaterial
is a function performed by
bridg:Specimen.performingMaterial
none
bridg:Specimen.performingMaterial
performingMaterial
bridg:Specimen.performingMaterial
false
bridg:Specimen.performingMaterial
Material
bridg:Specimen.performingMaterial
urn:CTRv1.0:Specimen.performing
bridg:Material.performedSpecimen
function as
bridg:Material.performedSpecimen
none
bridg:Material.performedSpecimen
performedSpecimen
bridg:Specimen.producingPerformedSpecimenCollection
be a result of
bridg:Specimen.producingPerformedSpecimenCollection
none
bridg:Specimen.producingPerformedSpecimenCollection
producingPerformedSpecimenCollection
bridg:Specimen.producingPerformedSpecimenCollection
false
bridg:Specimen.producingPerformedSpecimenCollection
PerformedSpecimenCollection
bridg:Specimen.producingPerformedSpecimenCollection
urn:CTRv1.0:Specimen.producing
bridg:PerformedSpecimenCollection.producedSpecimen
result in
bridg:PerformedSpecimenCollection.producedSpecimen
none
bridg:PerformedSpecimenCollection.producedSpecimen
producedSpecimen
bridg:StatisticalAnalysisPlanDocumentVersion.usedStatisticalAnalysisPlanVersion
is created from
bridg:StatisticalAnalysisPlanDocumentVersion.usedStatisticalAnalysisPlanVersion
none
bridg:StatisticalAnalysisPlanDocumentVersion.usedStatisticalAnalysisPlanVersion
usedStatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanDocumentVersion.usedStatisticalAnalysisPlanVersion
false
bridg:StatisticalAnalysisPlanDocumentVersion.usedStatisticalAnalysisPlanVersion
Identifies the version of a statistical analysis plan that is the basis for a version of a statistical analysis plan document.
StatisticalAnalysisPlanDocumentVersion
bridg:StatisticalAnalysisPlanDocumentVersion.usedStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:StatisticalAnalysisPlanVersion.
bridg:StatisticalAnalysisPlanVersion.createdStatisticalAnalysisPlanDocumentVersion
be used to create
bridg:StatisticalAnalysisPlanVersion.createdStatisticalAnalysisPlanDocumentVersion
none
bridg:StatisticalAnalysisPlanVersion.createdStatisticalAnalysisPlanDocumentVersion
createdStatisticalAnalysisPlanDocumentVersion
bridg:StatisticalAnalysisPlanVersion.addressedStudyProtocolVersion
addresses the statistical needs of
bridg:StatisticalAnalysisPlanVersion.addressedStudyProtocolVersion
none
bridg:StatisticalAnalysisPlanVersion.addressedStudyProtocolVersion
addressedStudyProtocolVersion
bridg:StatisticalAnalysisPlanVersion.addressedStudyProtocolVersion
false
bridg:StatisticalAnalysisPlanVersion.addressedStudyProtocolVersion
Identifies the version of the study protocol that is the basis for a statistical analysis plan version.
StatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersion.addressedStudyProtocolVersion
urn:Statistics_v1.0:StudyProtocolVersion.
bridg:StudyProtocolVersion.addressingStatisticalAnalysisPlanVersion
have statistical needs addressed by
bridg:StudyProtocolVersion.addressingStatisticalAnalysisPlanVersion
none
bridg:StudyProtocolVersion.addressingStatisticalAnalysisPlanVersion
addressingStatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersion.versionedStatisticalAnalysisPlan
is a version of
bridg:StatisticalAnalysisPlanVersion.versionedStatisticalAnalysisPlan
none
bridg:StatisticalAnalysisPlanVersion.versionedStatisticalAnalysisPlan
versionedStatisticalAnalysisPlan
bridg:StatisticalAnalysisPlanVersion.versionedStatisticalAnalysisPlan
false
bridg:StatisticalAnalysisPlanVersion.versionedStatisticalAnalysisPlan
Identifies the statistical analysis plan that is the basis for a statistical analysis plan version.
StatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersion.versionedStatisticalAnalysisPlan
urn:Statistics_v1.0:StatisticalAnalysisPlan.
bridg:StatisticalAnalysisPlan.versioningStatisticalAnalysisPlanVersion
has as a version
bridg:StatisticalAnalysisPlan.versioningStatisticalAnalysisPlanVersion
none
bridg:StatisticalAnalysisPlan.versioningStatisticalAnalysisPlanVersion
versioningStatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionModificationSummary.sourceStatisticalAnalysisPlanVersion
has as source
bridg:StatisticalAnalysisPlanVersionModificationSummary.sourceStatisticalAnalysisPlanVersion
none
bridg:StatisticalAnalysisPlanVersionModificationSummary.sourceStatisticalAnalysisPlanVersion
sourceStatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionModificationSummary.sourceStatisticalAnalysisPlanVersion
false
bridg:StatisticalAnalysisPlanVersionModificationSummary.sourceStatisticalAnalysisPlanVersion
Identifies the changed version of the statistical analysis plan that is used to create a statistical analysis plan version modification summary.
StatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionModificationSummary.sourceStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary.previous
bridg:StatisticalAnalysisPlanVersion.targetStatisticalAnalysisPlanVersionModificationSummary
be the source for
bridg:StatisticalAnalysisPlanVersion.targetStatisticalAnalysisPlanVersionModificationSummary
none
bridg:StatisticalAnalysisPlanVersion.targetStatisticalAnalysisPlanVersionModificationSummary
targetStatisticalAnalysisPlanVersionModificationSummary
bridg:StatisticalAnalysisPlanVersionModificationSummary.targetStatisticalAnalysisPlanVersion
has as target
bridg:StatisticalAnalysisPlanVersionModificationSummary.targetStatisticalAnalysisPlanVersion
none
bridg:StatisticalAnalysisPlanVersionModificationSummary.targetStatisticalAnalysisPlanVersion
targetStatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionModificationSummary.targetStatisticalAnalysisPlanVersion
false
bridg:StatisticalAnalysisPlanVersionModificationSummary.targetStatisticalAnalysisPlanVersion
Identifies the original version of the statistical analysis plan that is used to create a statistical analysis plan version modification summary.
StatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionModificationSummary.targetStatisticalAnalysisPlanVersion
urn:Statistics_v1.0:StatisticalAnalysisPlanVersionModificationSummary.revised
bridg:StatisticalAnalysisPlanVersion.sourceStatisticalAnalysisPlanVersionModificationSummary
be the target for
bridg:StatisticalAnalysisPlanVersion.sourceStatisticalAnalysisPlanVersionModificationSummary
none
bridg:StatisticalAnalysisPlanVersion.sourceStatisticalAnalysisPlanVersionModificationSummary
sourceStatisticalAnalysisPlanVersionModificationSummary
bridg:StatisticalAnalysisPlanVersionStatus.describedStatisticalAnalysisPlanVersion
describes
bridg:StatisticalAnalysisPlanVersionStatus.describedStatisticalAnalysisPlanVersion
none
bridg:StatisticalAnalysisPlanVersionStatus.describedStatisticalAnalysisPlanVersion
describedStatisticalAnalysisPlanVersion
bridg:StatisticalAnalysisPlanVersionStatus.describedStatisticalAnalysisPlanVersion
false
bridg:StatisticalAnalysisPlanVersionStatus.describedStatisticalAnalysisPlanVersion
Identifies the statuses at different points in time for a particular version of a statistical analysis plan.
bridg:StatisticalAnalysisPlanVersion.describingStatisticalAnalysisPlanVersionStatus
be described by
bridg:StatisticalAnalysisPlanVersion.describingStatisticalAnalysisPlanVersionStatus
none
bridg:StatisticalAnalysisPlanVersion.describingStatisticalAnalysisPlanVersionStatus
describingStatisticalAnalysisPlanVersionStatus
bridg:StratumGroup.characterizingDefinedStratificationCriterionPermissibleResult
is characterized by
bridg:StratumGroup.characterizingDefinedStratificationCriterionPermissibleResult
none
bridg:StratumGroup.characterizingDefinedStratificationCriterionPermissibleResult
characterizingDefinedStratificationCriterionPermissibleResult
bridg:StratumGroup.characterizingDefinedStratificationCriterionPermissibleResult
false
bridg:StratumGroup.characterizingDefinedStratificationCriterionPermissibleResult
DefinedStratificationCriterionPermissibleResult
bridg:StratumGroup.characterizingDefinedStratificationCriterionPermissibleResult
urn:CTRv1.0:StratumGroup.characterizing
bridg:DefinedStratificationCriterionPermissibleResult.characterizedStratumGroup
characterizes
bridg:DefinedStratificationCriterionPermissibleResult.characterizedStratumGroup
none
bridg:DefinedStratificationCriterionPermissibleResult.characterizedStratumGroup
characterizedStratumGroup
bridg:StratumGroup.describingStudyProtocolVersion
is defined by
bridg:StratumGroup.describingStudyProtocolVersion
none
bridg:StratumGroup.describingStudyProtocolVersion
describingStudyProtocolVersion
bridg:StratumGroup.describingStudyProtocolVersion
false
bridg:StratumGroup.describingStudyProtocolVersion
StratumGroup
bridg:StratumGroup.describingStudyProtocolVersion
urn:CTRPv3.8:StudyProtocol.
StudyProtocolVersion
bridg:StratumGroup.describingStudyProtocolVersion
urn:CTRv1.0:StratumGroup.describing
bridg:StudyProtocolVersion.describedStratumGroup
define
bridg:StudyProtocolVersion.describedStratumGroup
none
bridg:StudyProtocolVersion.describedStratumGroup
describedStratumGroup
bridg:StudyActivity.usedDefinedActivity
uses
bridg:StudyActivity.usedDefinedActivity
none
bridg:StudyActivity.usedDefinedActivity
usedDefinedActivity
bridg:StudyActivity.usedDefinedActivity
false
bridg:StudyActivity.usedDefinedActivity
Activity
bridg:StudyActivity.usedDefinedActivity
urn:CTRPv3.8:StudyProtocol.
DefinedActivity
bridg:StudyActivity.usedDefinedActivity
urn:CTRv1.0:StudyActivity.used
bridg:DefinedActivity.usingStudyActivity
be used by
bridg:DefinedActivity.usingStudyActivity
none
bridg:DefinedActivity.usingStudyActivity
usingStudyActivity
bridg:StudyActivity.usingStudyProtocolVersion
is used by
bridg:StudyActivity.usingStudyProtocolVersion
none
bridg:StudyActivity.usingStudyProtocolVersion
usingStudyProtocolVersion
bridg:StudyActivity.usingStudyProtocolVersion
false
bridg:StudyActivity.usingStudyProtocolVersion
StudyProtocolVersion
bridg:StudyActivity.usingStudyProtocolVersion
urn:CTRv1.0:StudyActivity.using
bridg:StudyActivity.usingStudyProtocolVersion
urn:HL7SD:PlannedStudy.Precondition1
bridg:StudyProtocolVersion.usedStudyActivity
use
bridg:StudyProtocolVersion.usedStudyActivity
none
bridg:StudyProtocolVersion.usedStudyActivity
usedStudyActivity
bridg:StudyAgent.evaluatingStudyProtocolVersion
is evaluated by
bridg:StudyAgent.evaluatingStudyProtocolVersion
none
bridg:StudyAgent.evaluatingStudyProtocolVersion
evaluatingStudyProtocolVersion
bridg:StudyAgent.evaluatingStudyProtocolVersion
false
bridg:StudyAgent.evaluatingStudyProtocolVersion
Study
bridg:StudyAgent.evaluatingStudyProtocolVersion
urn:CTRRr3:StudyAgent.evaluating
StudyProtocolVersion
bridg:StudyAgent.evaluatingStudyProtocolVersion
urn:CTRv1.0:StudyAgent.evaluating
bridg:StudyProtocolVersion.evaluatedStudyAgent
be evaluating
bridg:StudyProtocolVersion.evaluatedStudyAgent
none
bridg:StudyProtocolVersion.evaluatedStudyAgent
evaluatedStudyAgent
bridg:StudyAgent.performingProduct
is a function performed by
bridg:StudyAgent.performingProduct
none
bridg:StudyAgent.performingProduct
performingProduct
bridg:StudyAgent.performingProduct
false
bridg:StudyAgent.performingProduct
Product
bridg:StudyAgent.performingProduct
urn:CTRRr3:StudyAgent.performing
Product
bridg:StudyAgent.performingProduct
urn:CTRv1.0:StudyAgent.performing
bridg:Product.performedStudyAgent
function as
bridg:Product.performedStudyAgent
none
bridg:Product.performedStudyAgent
performedStudyAgent
bridg:StudyCondition.focuses_onStudyProtocolVersion
is the focus of
bridg:StudyCondition.focuses_onStudyProtocolVersion
none
bridg:StudyCondition.focuses_onStudyProtocolVersion
focuses onStudyProtocolVersion
bridg:StudyCondition.focuses_onStudyProtocolVersion
false
bridg:StudyCondition.focuses_onStudyProtocolVersion
StudyProtocol
bridg:StudyCondition.focuses_onStudyProtocolVersion
urn:CTRPv3.8:StudyDisease.
StudyProtocolVersion
bridg:StudyCondition.focuses_onStudyProtocolVersion
urn:CTRv1.0:StudyCondition.focuses_on
bridg:StudyProtocolVersion.investigatedStudyCondition
focus on
bridg:StudyProtocolVersion.investigatedStudyCondition
none
bridg:StudyProtocolVersion.investigatedStudyCondition
investigatedStudyCondition
bridg:StudyExecution.instantiatingStudyProtocol
is the execution of
bridg:StudyExecution.instantiatingStudyProtocol
none
bridg:StudyExecution.instantiatingStudyProtocol
instantiatingStudyProtocol
bridg:StudyExecution.instantiatingStudyProtocol
false
bridg:StudyExecution.instantiatingStudyProtocol
StudyProtocol
bridg:StudyExecution.instantiatingStudyProtocol
urn:CTRv1.0:StudyExecution.instantiating
bridg:StudyProtocol.instantiatedStudyExecution
be the plan for
bridg:StudyProtocol.instantiatedStudyExecution
none
bridg:StudyProtocol.instantiatedStudyExecution
instantiatedStudyExecution
bridg:StudyLegalSponsor.performingHealthcareProvider
be a function performed by
bridg:StudyLegalSponsor.performingHealthcareProvider
none
bridg:StudyLegalSponsor.performingHealthcareProvider
performingHealthcareProvider
bridg:StudyLegalSponsor.performingHealthcareProvider
false
bridg:StudyLegalSponsor.performingHealthcareProvider
HealthcareProvider
bridg:StudyLegalSponsor.performingHealthcareProvider
urn:CTRv1.0:StudyLegalSponsor.performing
bridg:HealthcareProvider.performedStudyLegalSponsor
function as
bridg:HealthcareProvider.performedStudyLegalSponsor
none
bridg:HealthcareProvider.performedStudyLegalSponsor
performedStudyLegalSponsor
bridg:StudyLegalSponsor.performingOrganization
be a function performed by
bridg:StudyLegalSponsor.performingOrganization
none
bridg:StudyLegalSponsor.performingOrganization
performingOrganization
bridg:StudyLegalSponsor.performingOrganization
false
bridg:StudyLegalSponsor.performingOrganization
Organization
bridg:StudyLegalSponsor.performingOrganization
urn:CTRv1.0:StudyLegalSponsor.performing
bridg:Organization.performedStudyLegalSponsor
function as
bridg:Organization.performedStudyLegalSponsor
none
bridg:Organization.performedStudyLegalSponsor
performedStudyLegalSponsor
bridg:StudyLegalSponsor.sponsoredStudyProtocolVersion
is responsible for
bridg:StudyLegalSponsor.sponsoredStudyProtocolVersion
none
bridg:StudyLegalSponsor.sponsoredStudyProtocolVersion
sponsoredStudyProtocolVersion
bridg:StudyLegalSponsor.sponsoredStudyProtocolVersion
false
bridg:StudyLegalSponsor.sponsoredStudyProtocolVersion
StudyProtocolVersion
bridg:StudyLegalSponsor.sponsoredStudyProtocolVersion
urn:CTRv1.0:StudyLegalSponsor.sponsored
bridg:StudyProtocolVersion.sponsoringStudyLegalSponsor
be the responsibility of
bridg:StudyProtocolVersion.sponsoringStudyLegalSponsor
none
bridg:StudyProtocolVersion.sponsoringStudyLegalSponsor
sponsoringStudyLegalSponsor
bridg:StudyObjective.involvingStudyProtocolVersion
is an aim of
bridg:StudyObjective.involvingStudyProtocolVersion
none
bridg:StudyObjective.involvingStudyProtocolVersion
involvingStudyProtocolVersion
bridg:StudyObjective.involvingStudyProtocolVersion
false
bridg:StudyObjective.involvingStudyProtocolVersion
StudyOutcomeMeasure
bridg:StudyObjective.involvingStudyProtocolVersion
urn:CTRPv3.8:StudyProtocol.
StudyObjective
bridg:StudyObjective.involvingStudyProtocolVersion
urn:CTRPv3.8:StudyProtocol.
Study
bridg:StudyObjective.involvingStudyProtocolVersion
urn:CTRRr3:StudyObjective.involving
StudyProtocolVersion
bridg:StudyObjective.involvingStudyProtocolVersion
urn:CTRv1.0:StudyObjective.involving
bridg:StudyProtocolVersion.involvedStudyObjective
aim to achieve
bridg:StudyProtocolVersion.involvedStudyObjective
none
bridg:StudyProtocolVersion.involvedStudyObjective
involvedStudyObjective
bridg:StudyOutcomeMeasure.measuredStudyObjective
measures
bridg:StudyOutcomeMeasure.measuredStudyObjective
none
bridg:StudyOutcomeMeasure.measuredStudyObjective
measuredStudyObjective
bridg:StudyOutcomeMeasure.measuredStudyObjective
false
bridg:StudyOutcomeMeasure.measuredStudyObjective
StudyObjective
bridg:StudyOutcomeMeasure.measuredStudyObjective
urn:CTRRr3:StudyOutcomeMeasure.measured
StudyObjective
bridg:StudyOutcomeMeasure.measuredStudyObjective
urn:CTRv1.0:StudyOutcomeMeasure.measured
bridg:StudyObjective.measuringStudyOutcomeMeasure
is measured by
bridg:StudyObjective.measuringStudyOutcomeMeasure
none
bridg:StudyObjective.measuringStudyOutcomeMeasure
measuringStudyOutcomeMeasure
bridg:StudyOverallStatus.describedStudyExecution
describes
bridg:StudyOverallStatus.describedStudyExecution
none
bridg:StudyOverallStatus.describedStudyExecution
describedStudyExecution
bridg:StudyOverallStatus.describedStudyExecution
false
bridg:StudyOverallStatus.describedStudyExecution
StudyOverallStatus
bridg:StudyOverallStatus.describedStudyExecution
urn:CTRPv3.8:StudyProtocol.
StudyExecution
bridg:StudyOverallStatus.describedStudyExecution
urn:CTRv1.0:StudyOverallStatus.described
bridg:StudyExecution.describingStudyOverallStatus
be described by
bridg:StudyExecution.describingStudyOverallStatus
none
bridg:StudyExecution.describingStudyOverallStatus
describingStudyOverallStatus
bridg:StudyOversightAuthority.overseenStudyExecution
oversee
bridg:StudyOversightAuthority.overseenStudyExecution
none
bridg:StudyOversightAuthority.overseenStudyExecution
overseenStudyExecution
bridg:StudyOversightAuthority.overseenStudyExecution
false
bridg:StudyOversightAuthority.overseenStudyExecution
bridg:StudyOversightAuthority.overseenStudyExecution
urn:CTRPv1.0:InterventionalStudyProtocol.dataMonitoringCommitteeAppointedIndicator
bridg:StudyOversightAuthority.overseenStudyExecution
urn:CTRPv1.0:ObservationalStudyProtocol.dataMonitoringCommitteeAppointedIndicator
bridg:StudyOversightAuthority.overseenStudyExecution
urn:CTRPv1.0:StudyProtocol.dataMonitoringCommitteeAppointedIndicator
StudyExecution
bridg:StudyOversightAuthority.overseenStudyExecution
urn:CTRv1.0:StudyOversightAuthority.overseen
bridg:StudyExecution.overseeingStudyOversightAuthority
be overseen by
bridg:StudyExecution.overseeingStudyOversightAuthority
none
bridg:StudyExecution.overseeingStudyOversightAuthority
overseeingStudyOversightAuthority
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
oversee
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
none
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
overseenStudyProtocolVersion
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
false
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
StudyProtocol
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
urn:CTRPv3.8:StudyRegulatoryAuthority.
StudyProtocolVersion
bridg:StudyOversightAuthority.overseenStudyProtocolVersion
urn:CTRv1.0:StudyOversightAuthority.overseen
bridg:StudyProtocolVersion.overseeingStudyOversightAuthority
be overseen by
bridg:StudyProtocolVersion.overseeingStudyOversightAuthority
none
bridg:StudyProtocolVersion.overseeingStudyOversightAuthority
overseeingStudyOversightAuthority
bridg:StudyOversightAuthority.performingOversightAuthority
is a function performed by
bridg:StudyOversightAuthority.performingOversightAuthority
none
bridg:StudyOversightAuthority.performingOversightAuthority
performingOversightAuthority
bridg:StudyOversightAuthority.performingOversightAuthority
false
bridg:StudyOversightAuthority.performingOversightAuthority
OversightAuthority
bridg:StudyOversightAuthority.performingOversightAuthority
urn:CTRv1.0:StudyOversightAuthority.performing
bridg:OversightAuthority.performedStudyOversightAuthority
function as
bridg:OversightAuthority.performedStudyOversightAuthority
none
bridg:OversightAuthority.performedStudyOversightAuthority
performedStudyOversightAuthority
bridg:StudyPersonnel.performedStudyExecution
perform a role for
bridg:StudyPersonnel.performedStudyExecution
none
bridg:StudyPersonnel.performedStudyExecution
performedStudyExecution
bridg:StudyPersonnel.performedStudyExecution
false
bridg:StudyPersonnel.performedStudyExecution
StudyExecution
bridg:StudyPersonnel.performedStudyExecution
urn:CTRv1.0:StudyPersonnel.performed
bridg:StudyExecution.performingStudyPersonnel
have a role performed by
bridg:StudyExecution.performingStudyPersonnel
none
bridg:StudyExecution.performingStudyPersonnel
performingStudyPersonnel
bridg:StudyPersonnel.performingHealthcareProvider
be a function performed by
bridg:StudyPersonnel.performingHealthcareProvider
none
bridg:StudyPersonnel.performingHealthcareProvider
performingHealthcareProvider
bridg:StudyPersonnel.performingHealthcareProvider
false
bridg:StudyPersonnel.performingHealthcareProvider
Indicates that the StudyPersonnel role is being fulfilled by a HealthcareProvider
bridg:HealthcareProvider.performedStudyPersonnel
function as
bridg:HealthcareProvider.performedStudyPersonnel
none
bridg:HealthcareProvider.performedStudyPersonnel
performedStudyPersonnel
bridg:StudyPersonnel.performingResearchStaff
be a function performed by
bridg:StudyPersonnel.performingResearchStaff
none
bridg:StudyPersonnel.performingResearchStaff
performingResearchStaff
bridg:StudyPersonnel.performingResearchStaff
false
bridg:StudyPersonnel.performingResearchStaff
ResearchStaff
bridg:StudyPersonnel.performingResearchStaff
urn:CTRRr3:StudyColleague.performing
ResearchStaff
bridg:StudyPersonnel.performingResearchStaff
urn:CTRv1.0:StudyPersonnel.performing
bridg:ResearchStaff.performedStudyPersonnel
function as
bridg:ResearchStaff.performedStudyPersonnel
none
bridg:ResearchStaff.performedStudyPersonnel
performedStudyPersonnel
bridg:StudyPersonnel.performingStudyProtocolVersion
perform a role for
bridg:StudyPersonnel.performingStudyProtocolVersion
none
bridg:StudyPersonnel.performingStudyProtocolVersion
performingStudyProtocolVersion
bridg:StudyPersonnel.performingStudyProtocolVersion
false
bridg:StudyPersonnel.performingStudyProtocolVersion
Study
bridg:StudyPersonnel.performingStudyProtocolVersion
urn:CTRRr3:StudyColleague.communicated
StudyProtocolVersion
bridg:StudyPersonnel.performingStudyProtocolVersion
urn:CTRv1.0:StudyPersonnel.performing
bridg:StudyProtocolVersion.performedStudyPersonnel
have a role performed by
bridg:StudyProtocolVersion.performedStudyPersonnel
none
bridg:StudyProtocolVersion.performedStudyPersonnel
performedStudyPersonnel
bridg:StudyProtocolDocument.representedStudyProtocol
represents
bridg:StudyProtocolDocument.representedStudyProtocol
none
bridg:StudyProtocolDocument.representedStudyProtocol
representedStudyProtocol
bridg:StudyProtocolDocument.representedStudyProtocol
false
bridg:StudyProtocolDocument.representedStudyProtocol
StudyProtocol
bridg:StudyProtocolDocument.representedStudyProtocol
urn:CTRPv3.8:Document.studyProtocolIdentifier
StudyProtocol
bridg:StudyProtocolDocument.representedStudyProtocol
urn:CTRv1.0:StudyProtocolDocument.represented
bridg:StudyProtocol.representingStudyProtocolDocument
be represented in
bridg:StudyProtocol.representingStudyProtocolDocument
none
bridg:StudyProtocol.representingStudyProtocolDocument
representingStudyProtocolDocument
bridg:StudyProtocolDocumentVersion.containedStudyProtocolVersion
contains
bridg:StudyProtocolDocumentVersion.containedStudyProtocolVersion
none
bridg:StudyProtocolDocumentVersion.containedStudyProtocolVersion
containedStudyProtocolVersion
bridg:StudyProtocolDocumentVersion.containedStudyProtocolVersion
false
bridg:StudyProtocolDocumentVersion.containedStudyProtocolVersion
bridg:StudyProtocolVersion.containingStudyProtocolDocumentVersion
be the contents of
bridg:StudyProtocolVersion.containingStudyProtocolDocumentVersion
none
bridg:StudyProtocolVersion.containingStudyProtocolDocumentVersion
containingStudyProtocolDocumentVersion
bridg:StudyProtocolVersion.versionedStudyProtocol
is a version of
bridg:StudyProtocolVersion.versionedStudyProtocol
none
bridg:StudyProtocolVersion.versionedStudyProtocol
versionedStudyProtocol
bridg:StudyProtocolVersion.versionedStudyProtocol
false
bridg:StudyProtocolVersion.versionedStudyProtocol
StudyProtocol
bridg:StudyProtocolVersion.versionedStudyProtocol
urn:CTRv1.0:StudyProtocolVersion.versioned
StudyProtocol
bridg:StudyProtocolVersion.versionedStudyProtocol
urn:Statistics_v1.0:StudyProtocolVersion.versionedStudyProtocol
bridg:StudyProtocol.versioningStudyProtocolVersion
has as a version
bridg:StudyProtocol.versioningStudyProtocolVersion
none
bridg:StudyProtocol.versioningStudyProtocolVersion
versioningStudyProtocolVersion
bridg:StudyRecruitmentStatus.describedStudyExecution
describes
bridg:StudyRecruitmentStatus.describedStudyExecution
none
bridg:StudyRecruitmentStatus.describedStudyExecution
describedStudyExecution
bridg:StudyRecruitmentStatus.describedStudyExecution
false
bridg:StudyRecruitmentStatus.describedStudyExecution
StudyRecruitmentStatus
bridg:StudyRecruitmentStatus.describedStudyExecution
urn:CTRPv3.8:StudyProtocol.
Study
bridg:StudyRecruitmentStatus.describedStudyExecution
urn:CTRRr3:StudyRecruitmentStatus.described
StudyExecution
bridg:StudyRecruitmentStatus.describedStudyExecution
urn:CTRv1.0:StudyRecruitmentStatus.described
bridg:StudyExecution.describingStudyRecruitmentStatus
be described by
bridg:StudyExecution.describingStudyRecruitmentStatus
none
bridg:StudyExecution.describingStudyRecruitmentStatus
describingStudyRecruitmentStatus
bridg:StudyReference.referencedStudyProtocolVersion
is referenced by
bridg:StudyReference.referencedStudyProtocolVersion
none
bridg:StudyReference.referencedStudyProtocolVersion
referencedStudyProtocolVersion
bridg:StudyReference.referencedStudyProtocolVersion
false
bridg:StudyReference.referencedStudyProtocolVersion
StudyReference
bridg:StudyReference.referencedStudyProtocolVersion
urn:CTRRr3:Study.referenced
StudyProtocolVersion
bridg:StudyReference.referencedStudyProtocolVersion
urn:CTRv1.0:StudyReference.referenced
bridg:StudyProtocolVersion.referencingStudyReference
refer to
bridg:StudyProtocolVersion.referencingStudyReference
none
bridg:StudyProtocolVersion.referencingStudyReference
referencingStudyReference
bridg:StudyRegistry.managingOrganization
be managed by
bridg:StudyRegistry.managingOrganization
none
bridg:StudyRegistry.managingOrganization
managingOrganization
bridg:StudyRegistry.managingOrganization
false
bridg:StudyRegistry.managingOrganization
Organization
bridg:StudyRegistry.managingOrganization
urn:CTRRr3:StudyRegistry.managing
Organization
bridg:StudyRegistry.managingOrganization
urn:CTRv1.0:StudyRegistry.managing
bridg:Organization.managedStudyRegistry
manage
bridg:Organization.managedStudyRegistry
none
bridg:Organization.managedStudyRegistry
managedStudyRegistry
bridg:StudyResource.usedResource
uses
bridg:StudyResource.usedResource
none
bridg:StudyResource.usedResource
usedResource
bridg:StudyResource.usedResource
false
bridg:StudyResource.usedResource
Resource
bridg:StudyResource.usedResource
urn:CTRRr3:StudyResource.associated
Resource
bridg:StudyResource.usedResource
urn:CTRv1.0:StudyResource.used
bridg:Resource.usingStudyResource
be used for
bridg:Resource.usingStudyResource
none
bridg:Resource.usingStudyResource
usingStudyResource
bridg:StudyResource.usingStudyExecution
be used for
bridg:StudyResource.usingStudyExecution
none
bridg:StudyResource.usingStudyExecution
usingStudyExecution
bridg:StudyResource.usingStudyExecution
false
bridg:StudyResource.usingStudyExecution
Study
bridg:StudyResource.usingStudyExecution
urn:CTRRr3:StudyResource.associated
StudyExecution
bridg:StudyResource.usingStudyExecution
urn:CTRv1.0:StudyResource.using
bridg:StudyExecution.usedStudyResource
use
bridg:StudyExecution.usedStudyResource
none
bridg:StudyExecution.usedStudyResource
usedStudyResource
bridg:StudyResource.usingStudyProtocolVersion
be used for
bridg:StudyResource.usingStudyProtocolVersion
none
bridg:StudyResource.usingStudyProtocolVersion
usingStudyProtocolVersion
bridg:StudyResource.usingStudyProtocolVersion
false
bridg:StudyResource.usingStudyProtocolVersion
StudyResourcing
bridg:StudyResource.usingStudyProtocolVersion
urn:CTRPv3.8:StudyProtocol.
StudyProtocolVersion
bridg:StudyResource.usingStudyProtocolVersion
urn:CTRv1.0:StudyResource.using
bridg:StudyProtocolVersion.usedStudyResource
use
bridg:StudyProtocolVersion.usedStudyResource
none
bridg:StudyProtocolVersion.usedStudyResource
usedStudyResource
bridg:StudySite.executedStudyExecution
execute
bridg:StudySite.executedStudyExecution
none
bridg:StudySite.executedStudyExecution
executedStudyExecution
bridg:StudySite.executedStudyExecution
false
bridg:StudySite.executedStudyExecution
Study
bridg:StudySite.executedStudyExecution
urn:CTRRr3:StudySite.executes
StudyExecution
bridg:StudySite.executedStudyExecution
urn:CTRv1.0:StudySite.executed
bridg:StudyExecution.executingStudySite
be executed at
bridg:StudyExecution.executingStudySite
none
bridg:StudyExecution.executingStudySite
executingStudySite
bridg:StudySite.performingHealthcareFacility
be a function performed by
bridg:StudySite.performingHealthcareFacility
none
bridg:StudySite.performingHealthcareFacility
performingHealthcareFacility
bridg:StudySite.performingHealthcareFacility
false
bridg:StudySite.performingHealthcareFacility
HealthcareFacility
bridg:StudySite.performingHealthcareFacility
urn:CTRv1.0:StudySite.performing
bridg:HealthcareFacility.performedStudySite
function as
bridg:HealthcareFacility.performedStudySite
none
bridg:HealthcareFacility.performedStudySite
performedStudySite
bridg:StudySite.performingOrganization
be a function performed by
bridg:StudySite.performingOrganization
none
bridg:StudySite.performingOrganization
performingOrganization
bridg:StudySite.performingOrganization
false
bridg:StudySite.performingOrganization
n:OrganizationFunctionalRole
bridg:StudySite.performingOrganization
urn:CTRPv3.8:StudySite.Is_a
Organization
bridg:StudySite.performingOrganization
urn:CTRRr3:StudySite.performing
Organization
bridg:StudySite.performingOrganization
urn:CTRv1.0:StudySite.performing
bridg:Organization.performedStudySite
function as
bridg:Organization.performedStudySite
none
bridg:Organization.performedStudySite
performedStudySite
bridg:StudySiteOversightStatus.assigningOversightCommittee
be assigned by
bridg:StudySiteOversightStatus.assigningOversightCommittee
none
bridg:StudySiteOversightStatus.assigningOversightCommittee
assigningOversightCommittee
bridg:StudySiteOversightStatus.assigningOversightCommittee
false
bridg:StudySiteOversightStatus.assigningOversightCommittee
OversightCommittee
bridg:StudySiteOversightStatus.assigningOversightCommittee
urn:CTRv1.0:StudySiteOversightStatus.assigning
bridg:OversightCommittee.assignedStudySiteOversightStatus
assign
bridg:OversightCommittee.assignedStudySiteOversightStatus
none
bridg:OversightCommittee.assignedStudySiteOversightStatus
assignedStudySiteOversightStatus
bridg:StudySiteOversightStatus.describedStudySiteProtocolVersionRelationship
describes
bridg:StudySiteOversightStatus.describedStudySiteProtocolVersionRelationship
none
bridg:StudySiteOversightStatus.describedStudySiteProtocolVersionRelationship
describedStudySiteProtocolVersionRelationship
bridg:StudySiteOversightStatus.describedStudySiteProtocolVersionRelationship
false
bridg:StudySiteOversightStatus.describedStudySiteProtocolVersionRelationship
StudySiteProtocolVersionRelationship
bridg:StudySiteOversightStatus.describedStudySiteProtocolVersionRelationship
urn:CTRv1.0:StudySiteOversightStatus.described
bridg:StudySiteProtocolVersionRelationship.describingStudySiteOversightStatus
be described by
bridg:StudySiteProtocolVersionRelationship.describingStudySiteOversightStatus
none
bridg:StudySiteProtocolVersionRelationship.describingStudySiteOversightStatus
describingStudySiteOversightStatus
bridg:StudySitePersonnel.performedStudySite
perform a role for
bridg:StudySitePersonnel.performedStudySite
none
bridg:StudySitePersonnel.performedStudySite
performedStudySite
bridg:StudySitePersonnel.performedStudySite
false
bridg:StudySitePersonnel.performedStudySite
StudySiteContact
bridg:StudySitePersonnel.performedStudySite
urn:CTRPv3.8:StudySite.
StudySite
bridg:StudySitePersonnel.performedStudySite
urn:CTRRr3:StudySiteContact.communicated
StudySite
bridg:StudySitePersonnel.performedStudySite
urn:CTRv1.0:StudySitePersonnel.performed
bridg:StudySite.performingStudySitePersonnel
have a role performed by
bridg:StudySite.performingStudySitePersonnel
none
bridg:StudySite.performingStudySitePersonnel
performingStudySitePersonnel
bridg:StudySitePersonnel.performingHealthcareProvider
be a function performed by
bridg:StudySitePersonnel.performingHealthcareProvider
none
bridg:StudySitePersonnel.performingHealthcareProvider
performingHealthcareProvider
bridg:StudySitePersonnel.performingHealthcareProvider
false
bridg:StudySitePersonnel.performingHealthcareProvider
Indicates that the StudySitePersonnel role is being fulfilled by a HealthcareProvider.
bridg:HealthcareProvider.performedStudySitePersonnel
function as
bridg:HealthcareProvider.performedStudySitePersonnel
none
bridg:HealthcareProvider.performedStudySitePersonnel
performedStudySitePersonnel
bridg:StudySitePersonnel.performingResearchStaff
be a function performed by
bridg:StudySitePersonnel.performingResearchStaff
none
bridg:StudySitePersonnel.performingResearchStaff
performingResearchStaff
bridg:StudySitePersonnel.performingResearchStaff
false
bridg:StudySitePersonnel.performingResearchStaff
n:PersonFunctionalRole
bridg:StudySitePersonnel.performingResearchStaff
urn:CTRPv3.8:StudySiteContact.Is_a
ResearchStaff
bridg:StudySitePersonnel.performingResearchStaff
urn:CTRRr3:StudySiteContact.performing
ResearchStaff
bridg:StudySitePersonnel.performingResearchStaff
urn:CTRv1.0:StudySitePersonnel.performing
bridg:ResearchStaff.performedStudySitePersonnel
function as
bridg:ResearchStaff.performedStudySitePersonnel
none
bridg:ResearchStaff.performedStudySitePersonnel
performedStudySitePersonnel
bridg:StudySitePersonnel.supportedPlannedStudySite
plan to perform a role for
bridg:StudySitePersonnel.supportedPlannedStudySite
none
bridg:StudySitePersonnel.supportedPlannedStudySite
supportedPlannedStudySite
bridg:StudySitePersonnel.supportedPlannedStudySite
false
bridg:StudySitePersonnel.supportedPlannedStudySite
PlannedStudySite
bridg:StudySitePersonnel.supportedPlannedStudySite
urn:CTRv1.0:StudySitePersonnel.supported
bridg:PlannedStudySite.supportsStudySitePersonnel
have a role planned to be performed by
bridg:PlannedStudySite.supportsStudySitePersonnel
none
bridg:PlannedStudySite.supportsStudySitePersonnel
supportsStudySitePersonnel
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
executes
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
none
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
executedStudyProtocolVersion
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
false
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
StudyProtocolVersion
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
urn:CTRv1.0:StudySubjectExperienceDocumentVersion.
StudyProtocolVersion
bridg:StudySiteProtocolVersionRelationship.executedStudyProtocolVersion
urn:CTRv1.0:StudySiteProtocolVersionRelationship.executed
bridg:StudyProtocolVersion.executingStudySiteProtocolVersionRelationship
be executed at
bridg:StudyProtocolVersion.executingStudySiteProtocolVersionRelationship
none
bridg:StudyProtocolVersion.executingStudySiteProtocolVersionRelationship
executingStudySiteProtocolVersionRelationship
bridg:StudySiteProtocolVersionRelationship.executingStudySite
is executed at
bridg:StudySiteProtocolVersionRelationship.executingStudySite
none
bridg:StudySiteProtocolVersionRelationship.executingStudySite
executingStudySite
bridg:StudySiteProtocolVersionRelationship.executingStudySite
false
bridg:StudySiteProtocolVersionRelationship.executingStudySite
StudySite
bridg:StudySiteProtocolVersionRelationship.executingStudySite
urn:CTRv1.0:StudySiteProtocolVersionRelationship.executing
bridg:StudySite.executedStudySiteProtocolVersionRelationship
execute
bridg:StudySite.executedStudySiteProtocolVersionRelationship
none
bridg:StudySite.executedStudySiteProtocolVersionRelationship
executedStudySiteProtocolVersionRelationship
bridg:StudySiteRecruitmentStatus.describedStudySite
describes
bridg:StudySiteRecruitmentStatus.describedStudySite
none
bridg:StudySiteRecruitmentStatus.describedStudySite
describedStudySite
bridg:StudySiteRecruitmentStatus.describedStudySite
false
bridg:StudySiteRecruitmentStatus.describedStudySite
Indicates the point-in-time recruitment status of a study from the perspective of the study site.
bridg:StudySite.describingStudySiteRecruitmentStatus
be described by
bridg:StudySite.describingStudySiteRecruitmentStatus
none
bridg:StudySite.describingStudySiteRecruitmentStatus
describingStudySiteRecruitmentStatus
bridg:StudySiteResource.usedResource
uses
bridg:StudySiteResource.usedResource
none
bridg:StudySiteResource.usedResource
usedResource
bridg:StudySiteResource.usedResource
false
bridg:StudySiteResource.usedResource
bridg:StudySiteResource.usedResource
DEFINITION:
EXAMPLE(S):
OTHER NAME(S):
NOTE(S):
bridg:Resource.usingStudySiteResource
be used for
bridg:Resource.usingStudySiteResource
none
bridg:Resource.usingStudySiteResource
usingStudySiteResource
bridg:StudySiteResource.usingStudySite
is used at
bridg:StudySiteResource.usingStudySite
none
bridg:StudySiteResource.usingStudySite
usingStudySite
bridg:StudySiteResource.usingStudySite
false
bridg:StudySiteResource.usingStudySite
Indicates resources intended to be or actually consumed by a particular study site.
bridg:StudySite.usedStudySiteResource
use
bridg:StudySite.usedStudySiteResource
none
bridg:StudySite.usedStudySiteResource
usedStudySiteResource
bridg:StudySpecificStatisticalAnalysisPlan.addressedStudyProtocol
addresses the statistical needs of
bridg:StudySpecificStatisticalAnalysisPlan.addressedStudyProtocol
none
bridg:StudySpecificStatisticalAnalysisPlan.addressedStudyProtocol
addressedStudyProtocol
bridg:StudySpecificStatisticalAnalysisPlan.addressedStudyProtocol
false
bridg:StudySpecificStatisticalAnalysisPlan.addressedStudyProtocol
Identifies the study protocol whose data is used in the study specific statistical analysis plan.
StudySpecificStatisticalAnalysisPlan
bridg:StudySpecificStatisticalAnalysisPlan.addressedStudyProtocol
urn:Statistics_v1.0:StudyProtocol.
bridg:StudyProtocol.addressingStudySpecificStatisticalAnalysisPlan
have statistical needs addressed by
bridg:StudyProtocol.addressingStudySpecificStatisticalAnalysisPlan
none
bridg:StudyProtocol.addressingStudySpecificStatisticalAnalysisPlan
addressingStudySpecificStatisticalAnalysisPlan
bridg:StudySubjectExperienceDocumentVersion.describedStudySubject
describes experience of
bridg:StudySubjectExperienceDocumentVersion.describedStudySubject
none
bridg:StudySubjectExperienceDocumentVersion.describedStudySubject
describedStudySubject
bridg:StudySubjectExperienceDocumentVersion.describedStudySubject
false
bridg:StudySubjectExperienceDocumentVersion.describedStudySubject
Indicates the subject whose experience is recounted in the study subject experience document.
bridg:StudySubject.describingStudySubjectExperienceDocumentVersion
have experience described by
bridg:StudySubject.describingStudySubjectExperienceDocumentVersion
none
bridg:StudySubject.describingStudySubjectExperienceDocumentVersion
describingStudySubjectExperienceDocumentVersion
bridg:StudySubjectProtocolVersionRelationship.assigningStudySiteProtocolVersionRelationship
is assigned to
bridg:StudySubjectProtocolVersionRelationship.assigningStudySiteProtocolVersionRelationship
none
bridg:StudySubjectProtocolVersionRelationship.assigningStudySiteProtocolVersionRelationship
assigningStudySiteProtocolVersionRelationship
bridg:StudySubjectProtocolVersionRelationship.assigningStudySiteProtocolVersionRelationship
false
bridg:StudySubjectProtocolVersionRelationship.assigningStudySiteProtocolVersionRelationship
StudySiteProtocolVersionRelationship
bridg:StudySubjectProtocolVersionRelationship.assigningStudySiteProtocolVersionRelationship
urn:CTRv1.0:StudySubjectProtocolVersionRelationship.assigning
bridg:StudySiteProtocolVersionRelationship.assignedStudySubjectProtocolVersionRelationship
be the assigned version for
bridg:StudySiteProtocolVersionRelationship.assignedStudySubjectProtocolVersionRelationship
none
bridg:StudySiteProtocolVersionRelationship.assignedStudySubjectProtocolVersionRelationship
assignedStudySubjectProtocolVersionRelationship
bridg:StudySubjectProtocolVersionRelationship.assigningStudySubject
is the assigned version for
bridg:StudySubjectProtocolVersionRelationship.assigningStudySubject
none
bridg:StudySubjectProtocolVersionRelationship.assigningStudySubject
assigningStudySubject
bridg:StudySubjectProtocolVersionRelationship.assigningStudySubject
false
bridg:StudySubjectProtocolVersionRelationship.assigningStudySubject
StudySubject
bridg:StudySubjectProtocolVersionRelationship.assigningStudySubject
urn:CTRv1.0:StudySubjectProtocolVersionRelationship.assigning
bridg:StudySubject.assignedStudySubjectProtocolVersionRelationship
be assigned to
bridg:StudySubject.assignedStudySubjectProtocolVersionRelationship
none
bridg:StudySubject.assignedStudySubjectProtocolVersionRelationship
assignedStudySubjectProtocolVersionRelationship
bridg:Subject.performingBiologicEntity
be a function performed by
bridg:Subject.performingBiologicEntity
none
bridg:Subject.performingBiologicEntity
performingBiologicEntity
bridg:Subject.performingBiologicEntity
false
bridg:Subject.performingBiologicEntity
n:PersonFunctionalRole
bridg:Subject.performingBiologicEntity
urn:CTRPv3.8:Subject.Is_a
BiologicEntity
bridg:Subject.performingBiologicEntity
urn:CTRv1.0:Subject.performing
bridg:BiologicEntity.performedSubject
function as
bridg:BiologicEntity.performedSubject
none
bridg:BiologicEntity.performedSubject
performedSubject
bridg:Subject.performingBiologicEntityGroup
be a function performed by
bridg:Subject.performingBiologicEntityGroup
none
bridg:Subject.performingBiologicEntityGroup
performingBiologicEntityGroup
bridg:Subject.performingBiologicEntityGroup
false
bridg:Subject.performingBiologicEntityGroup
Indicates that a particular group of biologic entities is the subject of a particular activity.
bridg:Subject.performingBiologicEntityGroup
Used when the activity is done to the group as a whole rather than individuals. E.g. drugs in shared feed, spraying, group therapy, etc.
bridg:BiologicEntityGroup.performedSubject
function as
bridg:BiologicEntityGroup.performedSubject
none
bridg:BiologicEntityGroup.performedSubject
performedSubject
bridg:Subject.performingOrganization
be a function performed by
bridg:Subject.performingOrganization
none
bridg:Subject.performingOrganization
performingOrganization
bridg:Subject.performingOrganization
false
bridg:Subject.performingOrganization
Indicates that the Organization is participating as the subject of an activity.
bridg:Subject.performingOrganization
Audit
bridg:Organization.performedSubject
function as
bridg:Organization.performedSubject
none
bridg:Organization.performedSubject
performedSubject
bridg:Subject.performingProduct
be a function performed by
bridg:Subject.performingProduct
none
bridg:Subject.performingProduct
performingProduct
bridg:Subject.performingProduct
false
bridg:Subject.performingProduct
Product
bridg:Subject.performingProduct
urn:CTRv1.0:Subject.performing
bridg:Product.performedSubject
function as
bridg:Product.performedSubject
none
bridg:Product.performedSubject
performedSubject
bridg:Subject.performingSpecimen
be a function performed by
bridg:Subject.performingSpecimen
none
bridg:Subject.performingSpecimen
performingSpecimen
bridg:Subject.performingSpecimen
false
bridg:Subject.performingSpecimen
Specimen
bridg:Subject.performingSpecimen
urn:CTRv1.0:Subject.performing
bridg:Specimen.performedSubject
function as
bridg:Specimen.performedSubject
none
bridg:Specimen.performedSubject
performedSubject
bridg:SubjectIdentifier.assigningDonorRegistry
be assigned by
bridg:SubjectIdentifier.assigningDonorRegistry
none
bridg:SubjectIdentifier.assigningDonorRegistry
assigningDonorRegistry
bridg:SubjectIdentifier.assigningDonorRegistry
false
bridg:SubjectIdentifier.assigningDonorRegistry
Indicates the donor registry that assigned the identifer.
bridg:DonorRegistry.assignedSubjectIdentifier
assign
bridg:DonorRegistry.assignedSubjectIdentifier
none
bridg:DonorRegistry.assignedSubjectIdentifier
assignedSubjectIdentifier
bridg:SubjectIdentifier.assigningOrganization
be assigned by
bridg:SubjectIdentifier.assigningOrganization
none
bridg:SubjectIdentifier.assigningOrganization
assigningOrganization
bridg:SubjectIdentifier.assigningOrganization
false
bridg:SubjectIdentifier.assigningOrganization
Organization
bridg:SubjectIdentifier.assigningOrganization
urn:CTRv1.0:SubjectIdentifier.assigning
bridg:Organization.assignedSubjectIdentifier
assign
bridg:Organization.assignedSubjectIdentifier
none
bridg:Organization.assignedSubjectIdentifier
assignedSubjectIdentifier
bridg:SubjectIdentifier.assigningSystemOfRecord
be assigned by
bridg:SubjectIdentifier.assigningSystemOfRecord
none
bridg:SubjectIdentifier.assigningSystemOfRecord
assigningSystemOfRecord
bridg:SubjectIdentifier.assigningSystemOfRecord
false
bridg:SubjectIdentifier.assigningSystemOfRecord
SystemOfRecord
bridg:SubjectIdentifier.assigningSystemOfRecord
urn:CTRv1.0:SubjectIdentifier.assigning
bridg:SystemOfRecord.assignedSubjectIdentifier
assign
bridg:SystemOfRecord.assignedSubjectIdentifier
none
bridg:SystemOfRecord.assignedSubjectIdentifier
assignedSubjectIdentifier
bridg:SubjectIdentifier.identifiedSubject
identifies
bridg:SubjectIdentifier.identifiedSubject
none
bridg:SubjectIdentifier.identifiedSubject
identifiedSubject
bridg:SubjectIdentifier.identifiedSubject
false
bridg:SubjectIdentifier.identifiedSubject
Subject
bridg:SubjectIdentifier.identifiedSubject
urn:CTRv1.0:SubjectIdentifier.identified
bridg:Subject.identifyingSubjectIdentifier
be identified by
bridg:Subject.identifyingSubjectIdentifier
none
bridg:Subject.identifyingSubjectIdentifier
identifyingSubjectIdentifier
bridg:Submission.describedProduct
has as subject
bridg:Submission.describedProduct
none
bridg:Submission.describedProduct
describedProduct
bridg:Submission.describedProduct
false
bridg:Submission.describedProduct
Product
bridg:Submission.describedProduct
urn:CTRRr3:Submission.described
Product
bridg:Submission.describedProduct
urn:CTRv1.0:Submission.described
bridg:Product.describingSubmission
be the subject for
bridg:Product.describingSubmission
none
bridg:Product.describingSubmission
describingSubmission
bridg:Submission.evaluatingRegulatoryAssessment
be evaluated in
bridg:Submission.evaluatingRegulatoryAssessment
none
bridg:Submission.evaluatingRegulatoryAssessment
evaluatingRegulatoryAssessment
bridg:Submission.evaluatingRegulatoryAssessment
false
bridg:Submission.evaluatingRegulatoryAssessment
RegulatoryAssessment
bridg:Submission.evaluatingRegulatoryAssessment
urn:CTRRr3:Submission.evaluating
RegulatoryAssessment
bridg:Submission.evaluatingRegulatoryAssessment
urn:CTRv1.0:Submission.evaluating
bridg:RegulatoryAssessment.evaluatedSubmission
evaluates
bridg:RegulatoryAssessment.evaluatedSubmission
none
bridg:RegulatoryAssessment.evaluatedSubmission
evaluatedSubmission
bridg:Submission.groupingRegulatoryApplication
is grouped by
bridg:Submission.groupingRegulatoryApplication
none
bridg:Submission.groupingRegulatoryApplication
groupingRegulatoryApplication
bridg:Submission.groupingRegulatoryApplication
false
bridg:Submission.groupingRegulatoryApplication
StudyIndIde
bridg:Submission.groupingRegulatoryApplication
urn:CTRPv3.8:StudyProtocol.
RegulatoryApplication
bridg:Submission.groupingRegulatoryApplication
urn:CTRRr3:Submission.grouping
RegulatoryApplication
bridg:Submission.groupingRegulatoryApplication
urn:CTRv1.0:Submission.grouping
bridg:RegulatoryApplication.groupedSubmission
groups
bridg:RegulatoryApplication.groupedSubmission
composite
bridg:RegulatoryApplication.groupedSubmission
groupedSubmission
bridg:Submission.submittingRegulatoryApplicationSponsor
is submitted by
bridg:Submission.submittingRegulatoryApplicationSponsor
none
bridg:Submission.submittingRegulatoryApplicationSponsor
submittingRegulatoryApplicationSponsor
bridg:Submission.submittingRegulatoryApplicationSponsor
false
bridg:Submission.submittingRegulatoryApplicationSponsor
RegulatoryApplicationSponsor
bridg:Submission.submittingRegulatoryApplicationSponsor
urn:CTRRr3:Submission.submitting
RegulatoryApplicationSponsor
bridg:Submission.submittingRegulatoryApplicationSponsor
urn:CTRv1.0:Submission.submitting
bridg:RegulatoryApplicationSponsor.submittedSubmission
submits
bridg:RegulatoryApplicationSponsor.submittedSubmission
none
bridg:RegulatoryApplicationSponsor.submittedSubmission
submittedSubmission
bridg:SubmissionUnit.groupingReviewableUnit
be grouped into
bridg:SubmissionUnit.groupingReviewableUnit
none
bridg:SubmissionUnit.groupingReviewableUnit
groupingReviewableUnit
bridg:SubmissionUnit.groupingReviewableUnit
false
bridg:SubmissionUnit.groupingReviewableUnit
ReviewableUnit
bridg:SubmissionUnit.groupingReviewableUnit
urn:CTRv1.0:SubmissionUnit.grouping
bridg:ReviewableUnit.groupedSubmissionUnit
groups
bridg:ReviewableUnit.groupedSubmissionUnit
composite
bridg:ReviewableUnit.groupedSubmissionUnit
groupedSubmissionUnit
bridg:SubmissionUnit.groupingSubmission
be grouped into
bridg:SubmissionUnit.groupingSubmission
none
bridg:SubmissionUnit.groupingSubmission
groupingSubmission
bridg:SubmissionUnit.groupingSubmission
false
bridg:SubmissionUnit.groupingSubmission
Submission
bridg:SubmissionUnit.groupingSubmission
urn:CTRRr3:SubmissionUnit.grouping
Submission
bridg:SubmissionUnit.groupingSubmission
urn:CTRv1.0:SubmissionUnit.grouping
bridg:Submission.groupedSubmissionUnit
group
bridg:Submission.groupedSubmissionUnit
composite
bridg:Submission.groupedSubmissionUnit
groupedSubmissionUnit
bridg:SubmissionUnit.includedDocumentVersion
includes
bridg:SubmissionUnit.includedDocumentVersion
none
bridg:SubmissionUnit.includedDocumentVersion
includedDocumentVersion
bridg:SubmissionUnit.includedDocumentVersion
false
bridg:SubmissionUnit.includedDocumentVersion
Submission
bridg:SubmissionUnit.includedDocumentVersion
urn:CTRPv3.8:StudyProtocol.
Document
bridg:SubmissionUnit.includedDocumentVersion
urn:CTRRr3:SubmissionUnit.included
DocumentVersion
bridg:SubmissionUnit.includedDocumentVersion
urn:CTRv1.0:SubmissionUnit.included
bridg:DocumentVersion.includingSubmissionUnit
be included in
bridg:DocumentVersion.includingSubmissionUnit
none
bridg:DocumentVersion.includingSubmissionUnit
includingSubmissionUnit
bridg:SubstanceExtractionAdministrationRelationship.producingPerformedSubstanceExtraction
uses a substance produced by
bridg:SubstanceExtractionAdministrationRelationship.producingPerformedSubstanceExtraction
none
bridg:SubstanceExtractionAdministrationRelationship.producingPerformedSubstanceExtraction
producingPerformedSubstanceExtraction
bridg:SubstanceExtractionAdministrationRelationship.producingPerformedSubstanceExtraction
false
bridg:SubstanceExtractionAdministrationRelationship.producingPerformedSubstanceExtraction
bridg:PerformedSubstanceExtraction.usedSubstanceExtractionAdministrationRelationship
be producing a substance later used in
bridg:PerformedSubstanceExtraction.usedSubstanceExtractionAdministrationRelationship
none
bridg:PerformedSubstanceExtraction.usedSubstanceExtractionAdministrationRelationship
usedSubstanceExtractionAdministrationRelationship
bridg:SubstanceExtractionAdministrationRelationship.usingPerformedSubstanceAdministration
be producing a substance later used in
bridg:SubstanceExtractionAdministrationRelationship.usingPerformedSubstanceAdministration
none
bridg:SubstanceExtractionAdministrationRelationship.usingPerformedSubstanceAdministration
usingPerformedSubstanceAdministration
bridg:SubstanceExtractionAdministrationRelationship.usingPerformedSubstanceAdministration
false
bridg:SubstanceExtractionAdministrationRelationship.usingPerformedSubstanceAdministration
bridg:PerformedSubstanceAdministration.producedSubstanceExtractionAdministrationRelationship
be using a substance produced by
bridg:PerformedSubstanceAdministration.producedSubstanceExtractionAdministrationRelationship
none
bridg:PerformedSubstanceAdministration.producedSubstanceExtractionAdministrationRelationship
producedSubstanceExtractionAdministrationRelationship
bridg:TargetAnatomicSite.describedPerformedObservationResult
described
bridg:TargetAnatomicSite.describedPerformedObservationResult
none
bridg:TargetAnatomicSite.describedPerformedObservationResult
describedPerformedObservationResult
bridg:TargetAnatomicSite.describedPerformedObservationResult
false
bridg:TargetAnatomicSite.describedPerformedObservationResult
Indicates result being described by a particular site.
bridg:PerformedObservationResult.describingTargetAnatomicSite
be described by
bridg:PerformedObservationResult.describingTargetAnatomicSite
none
bridg:PerformedObservationResult.describingTargetAnatomicSite
describingTargetAnatomicSite
bridg:TreatingSite.containingCooperativeGroup
be a member of
bridg:TreatingSite.containingCooperativeGroup
none
bridg:TreatingSite.containingCooperativeGroup
containingCooperativeGroup
bridg:TreatingSite.containingCooperativeGroup
false
bridg:TreatingSite.containingCooperativeGroup
bridg:CooperativeGroup.containedTreatingSite
have as a member
bridg:CooperativeGroup.containedTreatingSite
none
bridg:CooperativeGroup.containedTreatingSite
containedTreatingSite
bridg:TreatingSite.containingCooperativeGroupMember
be a member of
bridg:TreatingSite.containingCooperativeGroupMember
none
bridg:TreatingSite.containingCooperativeGroupMember
containingCooperativeGroupMember
bridg:TreatingSite.containingCooperativeGroupMember
false
bridg:TreatingSite.containingCooperativeGroupMember
bridg:CooperativeGroupMember.containedTreatingSite
has as a member
bridg:CooperativeGroupMember.containedTreatingSite
none
bridg:CooperativeGroupMember.containedTreatingSite
containedTreatingSite
bridg:TreatingSite.performingHealthcareFacility
is a function performed by
bridg:TreatingSite.performingHealthcareFacility
none
bridg:TreatingSite.performingHealthcareFacility
performingHealthcareFacility
bridg:TreatingSite.performingHealthcareFacility
false
bridg:TreatingSite.performingHealthcareFacility
bridg:HealthcareFacility.performedTreatingSite
function as
bridg:HealthcareFacility.performedTreatingSite
none
bridg:HealthcareFacility.performedTreatingSite
performedTreatingSite