Preferred Label : Clinical Trial Registry;
NCIt definition : A publicly available database of clinical trial summary information, which may include
purpose of the study, recruiting status, condition and medical product under study,
study design, trial phase, participation criteria, contact information, primary outcome
measure, and results.;
Alternative definition : CDISC-GLOSS: A web-based publicly accessible platform for providing structured information
about clinical trials. NOTE: Such registries help patients, family members, health
care professionals, researchers, and the public identify studies in which they might
participate. Some registries include clinical trial results. Examples include: EU
Clinical Trials Register (EU CTR), for studies in the EU or the EEA after 1 May 2001;
ClinicalTrials.gov, a web-based resource from the National Library of Medicine (NLM)
in the US. [After International Committee of Medical Journal Editors];
NCI Metathesaurus CUI : CL540463;
Origin ID : C142452;
UMLS CUI : C4684606;
Semantic type(s)
- concept_is_in_subset
