Research study consent 77602-1
LOINC Code
LOINC code | 77602-1 | ||||
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name | Research study consent | ||||
description | Informed consent document for a patient to participate in a research study. The consent is signed by the patient at the beginning of a (clinical) research study, including observational or interventional research. It contains the study ID, study description and procedures that the patient will undergo during the study. In addition to a signature, it may contain choices selected by the patient (e.g., later use of collected tissue samples for related research). | ||||
status | ACTIVE | ||||
Fully-Specified Name | |||||
component | Research study consent | ||||
property | Find = Finding | ||||
time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||||
system | {Setting} | ||||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||||
method | Patient | ||||
Additional Names | |||||
short name | Research study consent | ||||
Basic Attributes | |||||
class | DOC.ONTOLOGY | ||||
type | 2 Clinical | ||||
order vs. observation | Both | ||||
Associated Observations | |||||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||||
Member of these Groups | |||||
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History/Usage | |||||
first released | |||||
last updated | 2.67 | ||||
last change type | MIN - change to field other than name | ||||
change reason | Removed "Patient" from Long Common Name and Shortname. | ||||
Related Names | |||||
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