FHIR Release 3 (STU)

This page is part of the FHIR Specification (v3.0.2: STU 3). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B R4 R3

8.22 Resource ResearchStudy - Content

Regulated Clinical Research Information Management Work GroupMaturity Level: 0 DraftCompartments: Practitioner

A process where a researcher or organization plans and then executes a series of steps intended to increase the field of healthcare-related knowledge. This includes studies of safety, efficacy, comparative effectiveness and other information about medications, devices, therapies and other interventional and investigative techniques. A ResearchStudy involves the gathering of information about human or animal subjects.

This resource supports the HL7 mission to create and promote HL7 standards by developing RCRIM standards to improve or enhance information management during clinical research and regulatory evaluation of the safety, efficacy and quality of therapeutic products and procedures worldwide.

This resource is referenced by AdverseEvent and ResearchSubject

Structure

NameFlagsCard.TypeDescription & Constraintsdoco
.. ResearchStudy DomainResourceInvestigation to increase healthcare-related patient-independent knowledge
Elements defined in Ancestors: id, meta, implicitRules, language, text, contained, extension, modifierExtension
... identifier Σ0..*IdentifierBusiness Identifier for study
... title Σ0..1stringName for this study
... protocol Σ0..*Reference(PlanDefinition)Steps followed in executing study
... partOf Σ0..*Reference(ResearchStudy)Part of larger study
... status ?!Σ1..1codedraft | in-progress | suspended | stopped | completed | entered-in-error
ResearchStudyStatus (Required)
... category Σ0..*CodeableConceptClassifications for the study
... focus Σ0..*CodeableConceptDrugs, devices, conditions, etc. under study
... contact Σ0..*ContactDetailContact details for the study
... relatedArtifact 0..*RelatedArtifactReferences and dependencies
... keyword Σ0..*CodeableConceptUsed to search for the study
... jurisdiction Σ0..*CodeableConceptGeographic region(s) for study
Jurisdiction ValueSet (Extensible)
... description 0..1markdownWhat this is study doing
... enrollment Σ0..*Reference(Group)Inclusion & exclusion criteria
... period Σ0..1PeriodWhen the study began and ended
... sponsor Σ0..1Reference(Organization)Organization responsible for the study
... principalInvestigator Σ0..1Reference(Practitioner)The individual responsible for the study
... site Σ0..*Reference(Location)Location involved in study execution
... reasonStopped Σ0..1CodeableConceptReason for terminating study early
... note 0..*AnnotationComments made about the event
... arm 0..*BackboneElementDefined path through the study for a subject
.... name 1..1stringLabel for study arm
.... code 0..1CodeableConceptCategorization of study arm
.... description 0..1stringShort explanation of study path

doco Documentation for this format

UML Diagram (Legend)

ResearchStudy (DomainResource)Identifiers assigned to this research study by the sponsor or other systemsidentifier : Identifier [0..*]A short, descriptive user-friendly label for the studytitle : string [0..1]The set of steps expected to be performed as part of the execution of the studyprotocol : Reference [0..*] PlanDefinition A larger research study of which this particular study is a component or steppartOf : Reference [0..*] ResearchStudy The current state of the study (this element modifies the meaning of other elements)status : code [1..1] Codes that convey the current status of the research study (Strength=Required)ResearchStudyStatus! Codes categorizing the type of study such as investigational vs. observational, type of blinding, type of randomization, safety vs. efficacy, etccategory : CodeableConcept [0..*]The condition(s), medication(s), food(s), therapy(ies), device(s) or other concerns or interventions that the study is seeking to gain more information aboutfocus : CodeableConcept [0..*]Contact details to assist a user in learning more about or engaging with the studycontact : ContactDetail [0..*]Citations, references and other related documentsrelatedArtifact : RelatedArtifact [0..*]Key terms to aid in searching for or filtering the studykeyword : CodeableConcept [0..*]Indicates a country, state or other region where the study is taking placejurisdiction : CodeableConcept [0..*] Countries and regions within which this artifact is targeted for use (Strength=Extensible)Jurisdiction ValueSet+ A full description of how the study is being conducteddescription : markdown [0..1]Reference to a Group that defines the criteria for and quantity of subjects participating in the study. E.g. " 200 female Europeans between the ages of 20 and 45 with early onset diabetes"enrollment : Reference [0..*] Group Identifies the start date and the expected (or actual, depending on status) end date for the studyperiod : Period [0..1]The organization responsible for the execution of the studysponsor : Reference [0..1] Organization Indicates the individual who has primary oversite of the execution of the studyprincipalInvestigator : Reference [0..1] Practitioner Clinic, hospital or other healthcare location that is participating in the studysite : Reference [0..*] Location A description and/or code explaining the premature termination of the studyreasonStopped : CodeableConcept [0..1]Comments made about the event by the performer, subject or other participantsnote : Annotation [0..*]ArmUnique, human-readable label for this arm of the studyname : string [1..1]Categorization of study arm, e.g. experimental, active comparator, placebo comparatercode : CodeableConcept [0..1]A succinct description of the path through the study that would be followed by a subject adhering to this armdescription : string [0..1]Describes an expected sequence of events for one of the participants of a study. E.g. Exposure to drug A, wash-out, exposure to drug B, wash-out, follow-uparm[0..*]

XML Template

<ResearchStudy xmlns="http://hl7.org/fhir"> doco
 <!-- from Resource: id, meta, implicitRules, and language -->
 <!-- from DomainResource: text, contained, extension, and modifierExtension -->
 <identifier><!-- 0..* Identifier Business Identifier for study --></identifier>
 <title value="[string]"/><!-- 0..1 Name for this study -->
 <protocol><!-- 0..* Reference(PlanDefinition) Steps followed in executing study --></protocol>
 <partOf><!-- 0..* Reference(ResearchStudy) Part of larger study --></partOf>
 <status value="[code]"/><!-- 1..1 draft | in-progress | suspended | stopped | completed | entered-in-error -->
 <category><!-- 0..* CodeableConcept Classifications for the study --></category>
 <focus><!-- 0..* CodeableConcept Drugs, devices, conditions, etc. under study --></focus>
 <contact><!-- 0..* ContactDetail Contact details for the study --></contact>
 <relatedArtifact><!-- 0..* RelatedArtifact References and dependencies --></relatedArtifact>
 <keyword><!-- 0..* CodeableConcept Used to search for the study --></keyword>
 <jurisdiction><!-- 0..* CodeableConcept Geographic region(s) for study --></jurisdiction>
 <description value="[markdown]"/><!-- 0..1 What this is study doing -->
 <enrollment><!-- 0..* Reference(Group) Inclusion & exclusion criteria --></enrollment>
 <period><!-- 0..1 Period When the study began and ended --></period>
 <sponsor><!-- 0..1 Reference(Organization) Organization responsible for the study --></sponsor>
 <principalInvestigator><!-- 0..1 Reference(Practitioner) The individual responsible for the study --></principalInvestigator>
 <site><!-- 0..* Reference(Location) Location involved in study execution --></site>
 <reasonStopped><!-- 0..1 CodeableConcept Reason for terminating study early --></reasonStopped>
 <note><!-- 0..* Annotation Comments made about the event --></note>
 <arm>  <!-- 0..* Defined path through the study for a subject -->
  <name value="[string]"/><!-- 1..1 Label for study arm -->
  <code><!-- 0..1 CodeableConcept Categorization of study arm --></code>
  <description value="[string]"/><!-- 0..1 Short explanation of study path -->
 </arm>
</ResearchStudy>

JSON Template

{doco
  "resourceType" : "ResearchStudy",
  // from Resource: id, meta, implicitRules, and language
  // from DomainResource: text, contained, extension, and modifierExtension
  "identifier" : [{ Identifier }], // Business Identifier for study
  "title" : "<string>", // Name for this study
  "protocol" : [{ Reference(PlanDefinition) }], // Steps followed in executing study
  "partOf" : [{ Reference(ResearchStudy) }], // Part of larger study
  "status" : "<code>", // R!  draft | in-progress | suspended | stopped | completed | entered-in-error
  "category" : [{ CodeableConcept }], // Classifications for the study
  "focus" : [{ CodeableConcept }], // Drugs, devices, conditions, etc. under study
  "contact" : [{ ContactDetail }], // Contact details for the study
  "relatedArtifact" : [{ RelatedArtifact }], // References and dependencies
  "keyword" : [{ CodeableConcept }], // Used to search for the study
  "jurisdiction" : [{ CodeableConcept }], // Geographic region(s) for study
  "description" : "<markdown>", // What this is study doing
  "enrollment" : [{ Reference(Group) }], // Inclusion & exclusion criteria
  "period" : { Period }, // When the study began and ended
  "sponsor" : { Reference(Organization) }, // Organization responsible for the study
  "principalInvestigator" : { Reference(Practitioner) }, // The individual responsible for the study
  "site" : [{ Reference(Location) }], // Location involved in study execution
  "reasonStopped" : { CodeableConcept }, // Reason for terminating study early
  "note" : [{ Annotation }], // Comments made about the event
  "arm" : [{ // Defined path through the study for a subject
    "name" : "<string>", // R!  Label for study arm
    "code" : { CodeableConcept }, // Categorization of study arm
    "description" : "<string>" // Short explanation of study path
  }]
}

Turtle Template

@prefix fhir: <http://hl7.org/fhir/> .doco


[ a fhir:ResearchStudy;
  fhir:nodeRole fhir:treeRoot; # if this is the parser root

  # from Resource: .id, .meta, .implicitRules, and .language
  # from DomainResource: .text, .contained, .extension, and .modifierExtension
  fhir:ResearchStudy.identifier [ Identifier ], ... ; # 0..* Business Identifier for study
  fhir:ResearchStudy.title [ string ]; # 0..1 Name for this study
  fhir:ResearchStudy.protocol [ Reference(PlanDefinition) ], ... ; # 0..* Steps followed in executing study
  fhir:ResearchStudy.partOf [ Reference(ResearchStudy) ], ... ; # 0..* Part of larger study
  fhir:ResearchStudy.status [ code ]; # 1..1 draft | in-progress | suspended | stopped | completed | entered-in-error
  fhir:ResearchStudy.category [ CodeableConcept ], ... ; # 0..* Classifications for the study
  fhir:ResearchStudy.focus [ CodeableConcept ], ... ; # 0..* Drugs, devices, conditions, etc. under study
  fhir:ResearchStudy.contact [ ContactDetail ], ... ; # 0..* Contact details for the study
  fhir:ResearchStudy.relatedArtifact [ RelatedArtifact ], ... ; # 0..* References and dependencies
  fhir:ResearchStudy.keyword [ CodeableConcept ], ... ; # 0..* Used to search for the study
  fhir:ResearchStudy.jurisdiction [ CodeableConcept ], ... ; # 0..* Geographic region(s) for study
  fhir:ResearchStudy.description [ markdown ]; # 0..1 What this is study doing
  fhir:ResearchStudy.enrollment [ Reference(Group) ], ... ; # 0..* Inclusion & exclusion criteria
  fhir:ResearchStudy.period [ Period ]; # 0..1 When the study began and ended
  fhir:ResearchStudy.sponsor [ Reference(Organization) ]; # 0..1 Organization responsible for the study
  fhir:ResearchStudy.principalInvestigator [ Reference(Practitioner) ]; # 0..1 The individual responsible for the study
  fhir:ResearchStudy.site [ Reference(Location) ], ... ; # 0..* Location involved in study execution
  fhir:ResearchStudy.reasonStopped [ CodeableConcept ]; # 0..1 Reason for terminating study early
  fhir:ResearchStudy.note [ Annotation ], ... ; # 0..* Comments made about the event
  fhir:ResearchStudy.arm [ # 0..* Defined path through the study for a subject
    fhir:ResearchStudy.arm.name [ string ]; # 1..1 Label for study arm
    fhir:ResearchStudy.arm.code [ CodeableConcept ]; # 0..1 Categorization of study arm
    fhir:ResearchStudy.arm.description [ string ]; # 0..1 Short explanation of study path
  ], ...;
]

Changes since DSTU2

This resource did not exist in Release 2

This analysis is available as XML or JSON.

Structure

NameFlagsCard.TypeDescription & Constraintsdoco
.. ResearchStudy DomainResourceInvestigation to increase healthcare-related patient-independent knowledge
Elements defined in Ancestors: id, meta, implicitRules, language, text, contained, extension, modifierExtension
... identifier Σ0..*IdentifierBusiness Identifier for study
... title Σ0..1stringName for this study
... protocol Σ0..*Reference(PlanDefinition)Steps followed in executing study
... partOf Σ0..*Reference(ResearchStudy)Part of larger study
... status ?!Σ1..1codedraft | in-progress | suspended | stopped | completed | entered-in-error
ResearchStudyStatus (Required)
... category Σ0..*CodeableConceptClassifications for the study
... focus Σ0..*CodeableConceptDrugs, devices, conditions, etc. under study
... contact Σ0..*ContactDetailContact details for the study
... relatedArtifact 0..*RelatedArtifactReferences and dependencies
... keyword Σ0..*CodeableConceptUsed to search for the study
... jurisdiction Σ0..*CodeableConceptGeographic region(s) for study
Jurisdiction ValueSet (Extensible)
... description 0..1markdownWhat this is study doing
... enrollment Σ0..*Reference(Group)Inclusion & exclusion criteria
... period Σ0..1PeriodWhen the study began and ended
... sponsor Σ0..1Reference(Organization)Organization responsible for the study
... principalInvestigator Σ0..1Reference(Practitioner)The individual responsible for the study
... site Σ0..*Reference(Location)Location involved in study execution
... reasonStopped Σ0..1CodeableConceptReason for terminating study early
... note 0..*AnnotationComments made about the event
... arm 0..*BackboneElementDefined path through the study for a subject
.... name 1..1stringLabel for study arm
.... code 0..1CodeableConceptCategorization of study arm
.... description 0..1stringShort explanation of study path

doco Documentation for this format

UML Diagram (Legend)

ResearchStudy (DomainResource)Identifiers assigned to this research study by the sponsor or other systemsidentifier : Identifier [0..*]A short, descriptive user-friendly label for the studytitle : string [0..1]The set of steps expected to be performed as part of the execution of the studyprotocol : Reference [0..*] PlanDefinition A larger research study of which this particular study is a component or steppartOf : Reference [0..*] ResearchStudy The current state of the study (this element modifies the meaning of other elements)status : code [1..1] Codes that convey the current status of the research study (Strength=Required)ResearchStudyStatus! Codes categorizing the type of study such as investigational vs. observational, type of blinding, type of randomization, safety vs. efficacy, etccategory : CodeableConcept [0..*]The condition(s), medication(s), food(s), therapy(ies), device(s) or other concerns or interventions that the study is seeking to gain more information aboutfocus : CodeableConcept [0..*]Contact details to assist a user in learning more about or engaging with the studycontact : ContactDetail [0..*]Citations, references and other related documentsrelatedArtifact : RelatedArtifact [0..*]Key terms to aid in searching for or filtering the studykeyword : CodeableConcept [0..*]Indicates a country, state or other region where the study is taking placejurisdiction : CodeableConcept [0..*] Countries and regions within which this artifact is targeted for use (Strength=Extensible)Jurisdiction ValueSet+ A full description of how the study is being conducteddescription : markdown [0..1]Reference to a Group that defines the criteria for and quantity of subjects participating in the study. E.g. " 200 female Europeans between the ages of 20 and 45 with early onset diabetes"enrollment : Reference [0..*] Group Identifies the start date and the expected (or actual, depending on status) end date for the studyperiod : Period [0..1]The organization responsible for the execution of the studysponsor : Reference [0..1] Organization Indicates the individual who has primary oversite of the execution of the studyprincipalInvestigator : Reference [0..1] Practitioner Clinic, hospital or other healthcare location that is participating in the studysite : Reference [0..*] Location A description and/or code explaining the premature termination of the studyreasonStopped : CodeableConcept [0..1]Comments made about the event by the performer, subject or other participantsnote : Annotation [0..*]ArmUnique, human-readable label for this arm of the studyname : string [1..1]Categorization of study arm, e.g. experimental, active comparator, placebo comparatercode : CodeableConcept [0..1]A succinct description of the path through the study that would be followed by a subject adhering to this armdescription : string [0..1]Describes an expected sequence of events for one of the participants of a study. E.g. Exposure to drug A, wash-out, exposure to drug B, wash-out, follow-uparm[0..*]

XML Template

<ResearchStudy xmlns="http://hl7.org/fhir"> doco
 <!-- from Resource: id, meta, implicitRules, and language -->
 <!-- from DomainResource: text, contained, extension, and modifierExtension -->
 <identifier><!-- 0..* Identifier Business Identifier for study --></identifier>
 <title value="[string]"/><!-- 0..1 Name for this study -->
 <protocol><!-- 0..* Reference(PlanDefinition) Steps followed in executing study --></protocol>
 <partOf><!-- 0..* Reference(ResearchStudy) Part of larger study --></partOf>
 <status value="[code]"/><!-- 1..1 draft | in-progress | suspended | stopped | completed | entered-in-error -->
 <category><!-- 0..* CodeableConcept Classifications for the study --></category>
 <focus><!-- 0..* CodeableConcept Drugs, devices, conditions, etc. under study --></focus>
 <contact><!-- 0..* ContactDetail Contact details for the study --></contact>
 <relatedArtifact><!-- 0..* RelatedArtifact References and dependencies --></relatedArtifact>
 <keyword><!-- 0..* CodeableConcept Used to search for the study --></keyword>
 <jurisdiction><!-- 0..* CodeableConcept Geographic region(s) for study --></jurisdiction>
 <description value="[markdown]"/><!-- 0..1 What this is study doing -->
 <enrollment><!-- 0..* Reference(Group) Inclusion & exclusion criteria --></enrollment>
 <period><!-- 0..1 Period When the study began and ended --></period>
 <sponsor><!-- 0..1 Reference(Organization) Organization responsible for the study --></sponsor>
 <principalInvestigator><!-- 0..1 Reference(Practitioner) The individual responsible for the study --></principalInvestigator>
 <site><!-- 0..* Reference(Location) Location involved in study execution --></site>
 <reasonStopped><!-- 0..1 CodeableConcept Reason for terminating study early --></reasonStopped>
 <note><!-- 0..* Annotation Comments made about the event --></note>
 <arm>  <!-- 0..* Defined path through the study for a subject -->
  <name value="[string]"/><!-- 1..1 Label for study arm -->
  <code><!-- 0..1 CodeableConcept Categorization of study arm --></code>
  <description value="[string]"/><!-- 0..1 Short explanation of study path -->
 </arm>
</ResearchStudy>

JSON Template

{doco
  "resourceType" : "ResearchStudy",
  // from Resource: id, meta, implicitRules, and language
  // from DomainResource: text, contained, extension, and modifierExtension
  "identifier" : [{ Identifier }], // Business Identifier for study
  "title" : "<string>", // Name for this study
  "protocol" : [{ Reference(PlanDefinition) }], // Steps followed in executing study
  "partOf" : [{ Reference(ResearchStudy) }], // Part of larger study
  "status" : "<code>", // R!  draft | in-progress | suspended | stopped | completed | entered-in-error
  "category" : [{ CodeableConcept }], // Classifications for the study
  "focus" : [{ CodeableConcept }], // Drugs, devices, conditions, etc. under study
  "contact" : [{ ContactDetail }], // Contact details for the study
  "relatedArtifact" : [{ RelatedArtifact }], // References and dependencies
  "keyword" : [{ CodeableConcept }], // Used to search for the study
  "jurisdiction" : [{ CodeableConcept }], // Geographic region(s) for study
  "description" : "<markdown>", // What this is study doing
  "enrollment" : [{ Reference(Group) }], // Inclusion & exclusion criteria
  "period" : { Period }, // When the study began and ended
  "sponsor" : { Reference(Organization) }, // Organization responsible for the study
  "principalInvestigator" : { Reference(Practitioner) }, // The individual responsible for the study
  "site" : [{ Reference(Location) }], // Location involved in study execution
  "reasonStopped" : { CodeableConcept }, // Reason for terminating study early
  "note" : [{ Annotation }], // Comments made about the event
  "arm" : [{ // Defined path through the study for a subject
    "name" : "<string>", // R!  Label for study arm
    "code" : { CodeableConcept }, // Categorization of study arm
    "description" : "<string>" // Short explanation of study path
  }]
}

Turtle Template

@prefix fhir: <http://hl7.org/fhir/> .doco


[ a fhir:ResearchStudy;
  fhir:nodeRole fhir:treeRoot; # if this is the parser root

  # from Resource: .id, .meta, .implicitRules, and .language
  # from DomainResource: .text, .contained, .extension, and .modifierExtension
  fhir:ResearchStudy.identifier [ Identifier ], ... ; # 0..* Business Identifier for study
  fhir:ResearchStudy.title [ string ]; # 0..1 Name for this study
  fhir:ResearchStudy.protocol [ Reference(PlanDefinition) ], ... ; # 0..* Steps followed in executing study
  fhir:ResearchStudy.partOf [ Reference(ResearchStudy) ], ... ; # 0..* Part of larger study
  fhir:ResearchStudy.status [ code ]; # 1..1 draft | in-progress | suspended | stopped | completed | entered-in-error
  fhir:ResearchStudy.category [ CodeableConcept ], ... ; # 0..* Classifications for the study
  fhir:ResearchStudy.focus [ CodeableConcept ], ... ; # 0..* Drugs, devices, conditions, etc. under study
  fhir:ResearchStudy.contact [ ContactDetail ], ... ; # 0..* Contact details for the study
  fhir:ResearchStudy.relatedArtifact [ RelatedArtifact ], ... ; # 0..* References and dependencies
  fhir:ResearchStudy.keyword [ CodeableConcept ], ... ; # 0..* Used to search for the study
  fhir:ResearchStudy.jurisdiction [ CodeableConcept ], ... ; # 0..* Geographic region(s) for study
  fhir:ResearchStudy.description [ markdown ]; # 0..1 What this is study doing
  fhir:ResearchStudy.enrollment [ Reference(Group) ], ... ; # 0..* Inclusion & exclusion criteria
  fhir:ResearchStudy.period [ Period ]; # 0..1 When the study began and ended
  fhir:ResearchStudy.sponsor [ Reference(Organization) ]; # 0..1 Organization responsible for the study
  fhir:ResearchStudy.principalInvestigator [ Reference(Practitioner) ]; # 0..1 The individual responsible for the study
  fhir:ResearchStudy.site [ Reference(Location) ], ... ; # 0..* Location involved in study execution
  fhir:ResearchStudy.reasonStopped [ CodeableConcept ]; # 0..1 Reason for terminating study early
  fhir:ResearchStudy.note [ Annotation ], ... ; # 0..* Comments made about the event
  fhir:ResearchStudy.arm [ # 0..* Defined path through the study for a subject
    fhir:ResearchStudy.arm.name [ string ]; # 1..1 Label for study arm
    fhir:ResearchStudy.arm.code [ CodeableConcept ]; # 0..1 Categorization of study arm
    fhir:ResearchStudy.arm.description [ string ]; # 0..1 Short explanation of study path
  ], ...;
]

Changes since DSTU2

This resource did not exist in Release 2

This analysis is available as XML or JSON.

 

Alternate definitions: Master Definition (XML, JSON), XML Schema/Schematron (for ) + JSON Schema, ShEx (for Turtle)

PathDefinitionTypeReference
ResearchStudy.status Codes that convey the current status of the research studyRequiredResearchStudyStatus
ResearchStudy.category Codes that describe the type of research study. E.g. Study phase, Interventional/Observational, blinding type, etc.UnknownNo details provided yet
ResearchStudy.focus Codes for medications, devices, conditions and other interventionsUnknownNo details provided yet
ResearchStudy.keyword Words associated with the study that may be useful in discoveryUnknownNo details provided yet
ResearchStudy.jurisdiction Countries and regions within which this artifact is targeted for useExtensibleJurisdiction ValueSet

Search parameters for this resource. The common parameters also apply. See Searching for more information about searching in REST, messaging, and services.

NameTypeDescriptionExpressionIn Common
categorytokenClassifications for the studyResearchStudy.category
datedateWhen the study began and endedResearchStudy.period
focustokenDrugs, devices, conditions, etc. under studyResearchStudy.focus
identifiertokenBusiness Identifier for studyResearchStudy.identifier
jurisdictiontokenGeographic region(s) for studyResearchStudy.jurisdiction
keywordtokenUsed to search for the studyResearchStudy.keyword
partofreferencePart of larger studyResearchStudy.partOf
(ResearchStudy)
principalinvestigatorreferenceThe individual responsible for the studyResearchStudy.principalInvestigator
(Practitioner)
protocolreferenceSteps followed in executing studyResearchStudy.protocol
(PlanDefinition)
sitereferenceLocation involved in study executionResearchStudy.site
(Location)
sponsorreferenceOrganization responsible for the studyResearchStudy.sponsor
(Organization)
statustokendraft | in-progress | suspended | stopped | completed | entered-in-errorResearchStudy.status
titlestringName for this studyResearchStudy.title