StateChangeReason - HL7 Terminology (THO) v7.2.0

HL7 Terminology (THO)
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CodeSystem: StateChangeReason

Official URL: http://terminology.hl7.org/CodeSystem/state-change-reason		Version: 2.0.0	Highlight text changes?
Active as of 2026-03-05	Maturity Level: 1	Responsible: Health Level Seven International	Computable Name: StateChangeReason
Other Identifiers: OID:2.16.840.1.113883.4.642.1.0
Copyright/Legal: This material derives from the HL7 Terminology (THO). THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license.html

Indicates why the state of the subject changed.

This Code system is referenced in the definition of the following value sets:

StateChangeReason

Last updated: 2020-04-09 21:10:28+0000

Properties

This code system defines the following properties for its concepts

Name

Code

URI

Type

Description

Status

status

http://hl7.org/fhir/concept-properties#status

code

Designation of a concept's state. Normally is not populated unless the state is retired.

Concepts

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

Code	Display	Definition	Deprecated
unable-to-participate	Unable to Participate	The subject (ResearchSubject) is not able to take part in the ResearchStudy. Examples: subject has moved away; subject cannot drive and therefore unable to participate, etc.
unwilling-to-participate	Unwilling to Participate	The subject (ResearchSubject) is refusing to take part in the ResearchStudy. Note: Subject refusal is a synonymous term and is used in some studies.
screening-failure	Screening Failure	The failure of the potential subject (ResearchSubject) of meeting one or more criteria required for participation in a trial.
intervention-complete	Intervention Complete	The subject (ResearchSubject) has finished the planned protocol-specified treatment phase.
follow-up-complete	Follow-up Complete	The subject (ResearchSubject) has finished the planned protocol-specified follow-up phase.
adverse-event	Adverse Event	The subject (ResearchSubject) has experienced any unfavorable or unintended disease, sign, or symptom that is temporally associated with the use of a medical treatment or procedure and that may or may not be considered related to the medical treatment or procedure.
consent-withdrawn	Consent Withdrawn	The subject (ResearchSubject) has revoked permission to participate in the study or one or more components of the study.
non-compliance	Non-compliance	The subject (ResearchSubject) has failed to follow medical advice, take medication as directed, or adhere to a prescribed course of treatment.
informedConsentSigned	Informed consent signed	The subject (ResearchSubject) has signed informed consent.
intOrObsComplete	intervention or observation complete	intervention or observation complete.	Deprecated
death	Death	The subject (ResearchSubject) has died.