77602-1

LOINC 2.82

Research 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).

Component

  • Research study consent

Specimen / system

  • {Setting}

Class

  • DOC.ONTOLOGY

Property

  • Find

Scale

  • Doc

Method

  • Patient

Related names

  • DOC.ONT; Document; Finding; Findings; Form; Point in time; Random; Study report

Index terms

  • DOC.ONT
  • Document
  • Finding
  • Findings
  • Form
  • Point in time
  • Random
  • Study report