LOINC
Version 2.67

77602-1Research study consentActive

Term 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).
Source: Regenstrief LOINC

Part Description

LP66710-2   Patient
Clinical information generated by a patient, or a patient agent (proxy), acting in a non-clinical role to provide clinically relevant information. The patient agent may not have a legally defined relationship with the patient (e.g. a close friend). Source: Regenstrief LOINC

Fully-Specified Name

Component
Research study consent
Property
Find
Time
Pt
System
{Setting}
Scale
Doc
Method
Patient

Additional Names

Short Name
Research study consent

Basic Attributes

Class
DOC.ONTOLOGY
Type
Clinical
First Released
Version 2.52
Last Updated
Version 2.67
Change Reason
Removed "Patient" from Long Common Name and Shortname.
Order vs. Observation
Both

Member of these Groups

LG41826-5 {Setting}|ANYTypeofService|ANYKindofDocument|ANYRole|ANYSubjectMatterDomain
LG39005-0 Patient|ANYTypeOfService|ANYKindOfNote|ANYSetting

Language Variants Get Info

zh-CNChinese (CHINA)
调查研究同意书:发现:时间点:{环境}:文档型:患者
it-ITItalian (ITALY)
Studio di ricerca, consenso:Osservazione:Pt:{Setting}:Doc:Paziente

LOINC FHIR® API Example - CodeSystem Request Get Info

https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=77602-1