77602-1
ClinicalResearch study consent
Definition
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).
LOINC 6-Axis Classification
Component
Research study consent
Property
Find
Time Aspect
Pt
System
{Setting}
Scale Type
Doc
Method Type
Patient
Details
Class
DOC.ONTOLOGY
Order/Observation
Both
Short Name
Research study consent
Related Names
Frequently Asked Questions
What is LOINC code 77602-1?
LOINC code 77602-1 identifies "Research study consent". 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).
What does 77602-1 measure?
This code measures Research study consent in {Setting}. It belongs to the DOC.ONTOLOGY class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.