{"resourceType":"ValueSet","id":"v3-ClinicalResearchEventReason","language":"en","text":{"status":"extensions","div":"<div xmlns=\"http://www.w3.org/1999/xhtml\" xml:lang=\"en\" lang=\"en\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet v3-ClinicalResearchEventReason</b></p><a name=\"v3-ClinicalResearchEventReason\"> </a><a name=\"hcv3-ClinicalResearchEventReason\"> </a><a name=\"v3-ClinicalResearchEventReason-en-US\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Language: en</p></div><ul><li>Include these codes as defined in <a href=\"CodeSystem-v3-ActReason.html\"><code>http://terminology.hl7.org/CodeSystem/v3-ActReason</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-RET\">RET</a></td><td style=\"color: #cccccc\">retest</td><td>**Definition:**The event occurred so that a test or observation performed at a prior event could be performed again due to conditions set forth in the protocol.</td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-SCH\">SCH</a></td><td style=\"color: #cccccc\">scheduled</td><td>**Definition:**The event occurred due to it being scheduled in the research protocol.</td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-TRM\">TRM</a></td><td style=\"color: #cccccc\">termination</td><td>**Definition:**The event occurred in order to terminate the subject's participation in the study.</td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-UNS\">UNS</a></td><td style=\"color: #cccccc\">unscheduled</td><td>**Definition:**The event that occurred was initiated by a study participant (e.g. the subject or the investigator), and did not occur for protocol reasons.</td></tr></table></li></ul></div>"},"url":"http://terminology.hl7.org/ValueSet/v3-ClinicalResearchEventReason","identifier":[{"system":"urn:ietf:rfc:3986","value":"urn:oid:2.16.840.1.113883.1.11.19755"}],"version":"3.0.0","name":"ClinicalResearchEventReason","title":"ClinicalResearchEventReason","status":"active","experimental":false,"date":"2014-03-26","publisher":"Health Level Seven International","contact":[{"telecom":[{"system":"url","value":"http://hl7.org"},{"system":"email","value":"hq@HL7.org"}]}],"description":"**Definition:**Specifies the reason that an event occurred in a clinical research study.","copyright":"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","compose":{"include":[{"system":"http://terminology.hl7.org/CodeSystem/v3-ActReason","concept":[{"code":"RET"},{"code":"SCH"},{"code":"TRM"},{"code":"UNS"}]}]}}