Clinical Trial Final Report

Preferred Label : Clinical Trial Final Report;

NCIt related terms : CTrial Fin Rept Subcat; Reports; final report; Central Trial Final Reports Subcategory;

NCIt definition : Records containing any interim or final results, as well as clinical and statistical descriptions, presentations, analyses and interpretations of any therapeutic, prophylactic, or diagnostic agent used in human subjects in a clinical trial.;

Alternative definition : CDISC-GLOSS: A written description of a trial/study of any therapeutic, prophylactic, or diagnostic agent conducted in human subjects, in which the clinical and statistical description, presentations, and analyses are fully integrated into a single report. [ICH E3]; CareLex: Subcategory name for the eTMF domain used to classify clinical study report documents.;

Details

Origin ID

C115575;

UMLS CUI

C3889645;

Automatic exact mappings (from CISMeF team)
- Final report (record artifact) [SNOMED CT concept]
- Informing (procedure) [SNOMED CT concept]
- Rapport [LOINC component]
- Report [LOINC System]
- Report [EDAM data]
- Report [LOINC component]
- Report (record artifact) [SNOMED CT concept]
- Reported [LOINC method]
- Reported (qualifier value) [SNOMED CT concept]
- Reporter (occupation) [SNOMED CT concept]
- Reporting [ICNP action]
- report [MeSH concept]
- report [Radlex concept]
- report [OBI concept]
- report [IUPAC Term]
- reporter [SNOMED Notion]
- reporting [Blood Transfusion thesaurus concept]
- research report [MeSH Descriptor]
Semantic type(s)
- Intellectual Product [UMLS semantic type]
concept_is_in_subset
- CDISC Glossary Terminology [NCIt concept]
- CareLex eTMF Terminology [NCIt concept]
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

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