293,031 терминов и синонимов из MeSH и LOINC
Lang Dictionary CODE | LUI | preferred no |
SUI | preference Yes / No |
Terms, descriptions |
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CUI C0008976 | |||||||
Russian | Medical Subject Headings Russian | D002986 | L13064863 | preferred | S16027630 | Y | КЛИНИЧЕСКИЕ ИСПЫТАНИЯ КАК ТЕМА |
Russian | Medical Subject Headings Russian | D002986 | L13057054 | no | S16013504 | Y | KLINICHESKIE ISPYTANIIA KAK TEMA |
(CPTSP) CRISP Thesaurus | A0595050 | AT51218891 | controlled study designed to assess the safety and efficacy of new drugs, devices, treatments, or preventive measures in humans by comparing two or more interventions or regimens; prefer specific phase NTs. | ||||
Medical Subject Headings | A12999508 | AT235428477 | Works about pre-planned studies of the safety, efficacy, or optimum dosage schedule (if appropriate) of one or more diagnostic, therapeutic, or prophylactic drugs, devices, or techniques selected according to predetermined criteria of eligibility and observed for predefined evidence of favorable and unfavorable effects. This concept includes clinical trials conducted both in the U.S. and in other countries.. | ||||
NCI NCI Dictionary of Cancer Terms | A15559115 | AT198021752 | A type of research study that tests how well new medical approaches work in people. These studies test new methods of screening, prevention, diagnosis, or treatment of a disease. | ||||
NCI Thesaurus | A15559115 | AT205727200 | A research study that prospectively assigns human participants or groups of humans to one or more health-related interventions to evaluate the effects on health outcomes. | ||||
NCI Clinical Data Interchange Standards Consortium | A15559115 | AT230072582 | 1) A research investigation involving human subjects that is designed to answer specific questions about the safety and efficacy of a biomedical intervention (drug, treatment, device) or new ways of using a known drug, treatment, or device). 2) A research study in which one or more human subjects are prospectively assigned to one or more interventions (which may include placebo or other control) to evaluate the effects of those interventions on health-related biomedical or behavioral outcomes.(1. modified from ICH E6 Glossary, Directive 2001/20/EC. 2. NIH revised definition 2015) (CDISC Glossary) | ||||
NCI_CDISC-GLOSS | A15559115 | AT234296676 | A research investigation involving human subjects that is designed to answer specific questions about the safety and efficacy of a biomedical intervention (drug, treatment, device) or new ways of using a known drug, treatment, or device). NOTE: NIH Office of Science Policy further specifies that a clinical trial is a type of research study that prospectively assigns subjects to interventions, and the EU clinical trial regulations set forth 3 specific conditions, any one of which qualifies a study as a clinical trial. These conditions include applying diagnostic or monitoring procedures not used in normal clinical practice to subjects. [after ICH E6 [R2], EU CTR 2014] See also clinical study, clinical investigation. | ||||
HL7V3.0 | A19720585 | AT202331260 | To perform health care as part of the clinical trial protocol. | ||||
MEDLINEPLUS | A21143362 | AT210362702 | Clinical trials are research studies that test how well new medical approaches work in people. Each study answers scientific questions and tries to find better ways to prevent, screen for, diagnose, or treat a disease. Clinical trials may also compare a new treatment to a treatment that is already available. Every clinical trial has a protocol, or action plan, for conducting the trial. The plan describes what will be done in the study, how it will be conducted, and why each part of the study is necessary. Each study has its own rules about who can take part. Some studies need volunteers with a certain disease. Some need healthy people. Others want just men or just women. An Institutional Review Board (IRB) reviews, monitors, and approves many clinical trials. It is an independent committee of physicians, statisticians, and members of the community. Its role is to
In the United States, a clinical trial must have an IRB if it is studying a drug, biological product, or medical device that the Food and Drug Administration (FDA) regulates, or it is funded or carried out by the federal government. NIH: National Institutes of Health | ||||
MSHNOR | A26532742 | AT204261549 | Forhåndsplanlagte studier av sikkerhet, effekt eller optimale doseringsplaner (når hensiktsmessig) av ett eller flere diagnostiske, terapeutiske eller profylaktiske medikamenter, utstyr eller teknikker som velges ut fra forhåndsbestemte kriterier for valg og observasjoner i henhold til forhåndsdefinert evidens for gunstige og uheldige resultater. Dette konseptet inkluderer kliniske studier som foretas både i USA og i andre land. | ||||
(PSY) Psychological Index Terms | A7559678 | AT46117209 | Systematic, planned studies to evaluate the safety and efficacy of drugs, devices, or diagnostic or therapeutic practices. Used only when the methodology is the focus of discussion. |