Participation in Research Section Content
This is to flag participation in a clinical trial. PRSB Elements should be formatted as subheadings in any HTML sent.
|Section||Description||Card.||MRO*||FHIR Target and Guidance|
|Participation in research||The details of any research studies participated in.||O||Carried in the CodeableConcept of Composition.section.code FHIR element.|
|PRSB Element||Description||Card.||MRO*||FHIR Target and Guidance|
|Name of research study||Name of the research study/trial and/or drug/intervention||0 to 1||O||Record(s) of participation in clinical trial(s). Each record should include information about the trial and the patient's participation, as recorded by the clinician. Text only.|
|* M=Mandatory R=Required O=Optional|
Example Participation in Research Section
This text section should be linked to the following FHIR Resources to provide the textual information in a coded format.
- The ITK3 FHIR eDischarge does not currently support coded participation in research information.