Release 5 Draft Ballot

This page is part of the FHIR Specification (v4.6.0: R5 Draft Ballot - see ballot notes). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

4.3.16.342 Code System http://terminology.hl7.org/CodeSystem/state-change-reason

Biomedical Research and Regulation Work Group Maturity Level: 1Draft Use Context: Any

This is a code system defined by the FHIR project.

Summary

Defining URL:http://terminology.hl7.org/CodeSystem/state-change-reason
Version:4.6.0
Name:StateChangeReason
Title:StateChangeReason
Definition:

Indicates why the state of the subject changed.

Committee:Biomedical Research and Regulation Work Group
OID:2.16.840.1.113883.4.642.1.1477 (for OID based terminology systems)
Source ResourceXML / JSON

This Code system is used in the following value sets:

4.3.16.342.1 Content

This code system http://terminology.hl7.org/CodeSystem/state-change-reason defines the following codes:

CodeDisplayDefinition
adverseEvent adverse eventadverse event.
death death (adverse event)death (adverse event).
notEligible did not meet eligibility criteriadid not meet eligibility criteria.
eligibleButNo eligible but unwilling or unable to participateeligible but unwilling or unable to participate.
enrolled enrolled or registeredenrolled or registered.
exclusion exclusionexclusion.
followUpComplete follow-up completefollow-up complete.
inclusion inclusioninclusion.
informedConsentSigned Informed consent signedInformed consent signed.
intOrObsComplete intervention or observation completeintervention or observation complete.
nonCompliance non-compliancenon-compliance.
preReg pre-registered or slot reservedpre-registered or slot reserved.
refuseConsent refuse consentrefuse consent.
screenFailure screen failurescreen failure.
studyClosed study permanently closed to accrualstudy permanently closed to accrual.
studyTerminated study terminatedstudy terminated.
subjectRefusal subject refusalsubject refusal.
unwillingOrUnable unwilling or unable to participateunwilling or unable to participate.
withdrawnConsent withdrawn consentwithdrawn consent.
diseaseRelapse Disease RelapseRelapse of disease.
failedRandomization Failed RandomizationSubject failed randomization.
lackOfEfficacy Lack Of EfficacyThe study activities were not efficient in dealing with the underlying issue.
lostToFollowUp Lost To Follow UpThe subject can no longer be followed up.
physicianDecision Physician DecisionA physician has decided the subject should no longer continue on the study.
pregnancy PregnancySubject is now pregnant and no longer meets the inclusion criteria.
progressiveDisease Progressive DiseaseThe subject has a disease that has progressed to far to allow them to continue in the study.
protocolDeviation Protocol DeviationThere has been a protocol deviation that cannot be corrected or compensated for.
recovery RecoveryThe subject has recovered and no longer meets the inclusion criteria.
siteTerminated Site TerminatedThe site where the subject was being treated is no longer in the study.
technicalProblems Technical ProblemsThe subject cannot continue on the study due to technical issues.
complete CompleteThe study is now complete.

 

See the full registry of code systems defined as part of FHIR.

Explanation of the columns that may appear on this page:

LevelA few code lists that FHIR defines are hierarchical - each code is assigned a level. See Code System for further information.
SourceThe source of the definition of the code (when the value set draws in codes defined elsewhere)
CodeThe code (used as the code in the resource instance). If the code is in italics, this indicates that the code is not selectable ('Abstract')
DisplayThe display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
DefinitionAn explanation of the meaning of the concept
CommentsAdditional notes about how to use the code