CDISC MRCT Center Clinical Research Glossary

Preferred Label : CDISC MRCT Center Clinical Research Glossary;

NCIt synonyms : MRCT-Ctr;

NCIt related terms : MRCT Center Clinical Research Glossary;

NCIt definition : The terminology relevant to the plain language glossary of CDISC and the Multi-Regional Clinical Trial (MRCT) Center of Brigham and Women's Hospital and Harvard.;

Alternative definition : MRCT-Ctr: The terminology relevant to the plain language glossary of the Multi-Regional Clinical Trial (MRCT) Center of Brigham and Women's Hospital and Harvard.;

NCI Metathesaurus CUI : CL1926545;

Details

Origin ID

C203912;

UMLS CUI

C5907824;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
concept_is_in_subset
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
subset_includes_concept
- Additive Effect [NCIt concept]
- Adherence [NCIt concept]
- Adverse Event [NCIt concept]
- Adverse Reaction [NCIt concept]
- Agender Identity [NCIt concept]
- Anonymization [NCIt concept]
- Antibody [NCIt concept]
- Antigen [NCIt concept]
- Arithmetic Mean [NCIt concept]
- Aromantic [NCIt concept]
- Asexual [NCIt concept]
- Assent Form [NCIt concept]
- Assessment [NCIt concept]
- Baseline Assessment [NCIt concept]
- Basket Trial [NCIt concept]
- Benefits of a Research Study [NCIt concept]
- Best Practice [NCIt concept]
- Bias [NCIt concept]
- Biomarker [NCIt concept]
- Cisgender Man [NCIt concept]
- Cisgender Woman [NCIt concept]
- Clinical Benefit [NCIt concept]
- Clinical Coordinator [NCIt concept]
- Clinical Generalizability [NCIt concept]
- Clinical Intervention or Procedure [NCIt concept]
- Clinical Research and Development [NCIt concept]
- Clinical Study Sponsor [NCIt concept]
- Clinical Trial [NCIt concept]
- Clinical Trial Eligibility Criteria [NCIt concept]
- Clinical Trial Objective [NCIt concept]
- Clinical Trial Protocol [NCIt concept]
- Clinician [NCIt concept]
- Cohort [NCIt concept]
- Comparative Effectiveness Research [NCIt concept]
- Comparator [NCIt concept]
- Computed Tomography [NCIt concept]
- Concomitant Agent [NCIt concept]
- Confidence Interval [NCIt concept]
- Confidentiality [NCIt concept]
- Confounding Effect [NCIt concept]
- Confounding Variable [NCIt concept]
- Consent Form [NCIt concept]
- Continued Access Study [NCIt concept]
- Contraception [NCIt concept]
- Contract Research Organization [NCIt concept]
- Control Group [NCIt concept]
- Correlation [NCIt concept]
- Data [NCIt concept]
- Data Monitoring Committee [NCIt concept]
- Diagnostic Sensitivity [NCIt concept]
- Diagnostic Specificity [NCIt concept]
- Disease Progression [NCIt concept]
- Disease-Free Survival [NCIt concept]
- Double Blind Study [NCIt concept]
- Drug Holiday [NCIt concept]
- Drug Withdrawn [NCIt concept]
- Effectiveness [NCIt concept]
- Efficacy [NCIt concept]
- Electronic Consent Form [NCIt concept]
- Emergency Use Authorization [NCIt concept]
- End Point [NCIt concept]
- Enrollment [NCIt concept]
- Epidemiologist [NCIt concept]
- Equivalence Trial [NCIt concept]
- Equivalent Effect [NCIt concept]
- Exclusion Criteria [NCIt concept]
- Expanded Access Study [NCIt concept]
- Exploratory Research [NCIt concept]
- Focus Group [NCIt concept]
- Gender Fluid [NCIt concept]
- Genderqueer [NCIt concept]
- Genetic Testing [NCIt concept]
- Hazard Ratio [NCIt concept]
- Healthy Subject [NCIt concept]
- Hereditary [NCIt concept]
- Heterosexuality [NCIt concept]
- Immune Response Process [NCIt concept]
- Incidence [NCIt concept]
- Inclusion Criteria [NCIt concept]
- Informed Assent [NCIt concept]
- Informed Consent [NCIt concept]
- Infusion Procedure [NCIt concept]
- Institutional Review Board [NCIt concept]
- Investigational Medicinal Product [NCIt concept]
- Investigational New Drug Application [NCIt concept]
- Investigator [NCIt concept]
- Lesbian [NCIt concept]
- Longitudinal Study [NCIt concept]
- Magnetic Resonance Imaging [NCIt concept]
- Master Protocol [NCIt concept]
- Maximum [NCIt concept]
- Median [NCIt concept]
- Minimum [NCIt concept]
- Minor Person [NCIt concept]
- Monitoring [NCIt concept]
- Morbidity Rate [NCIt concept]
- Mortality Rate [NCIt concept]
- Multi-Institutional Clinical Trial [NCIt concept]
- Negative Test Result [NCIt concept]
- Negligible [NCIt concept]
- Non-Binary Gender Identity [NCIt concept]
- Non-Inferiority Trial [NCIt concept]
- Observational Study [NCIt concept]
- Odds Ratio [NCIt concept]
- Off-Label Treatment [NCIt concept]
- Open Label Study [NCIt concept]
- P-Value [NCIt concept]
- Pansexuality [NCIt concept]
- Patient Compliance [NCIt concept]
- Patient Reported Outcome [NCIt concept]
- Peer Review [NCIt concept]
- Pharmacodynamic Study [NCIt concept]
- Pharmacokinetics [NCIt concept]
- Pharmacotherapy [NCIt concept]
- Pharmacovigilance [NCIt concept]
- Phlebotomy [NCIt concept]
- Physical Medical Procedure [NCIt concept]
- Pilot Study [NCIt concept]
- Placebo [NCIt concept]
- Placebo-Controlled Study [NCIt concept]
- Platform Trial [NCIt concept]
- Positive Finding [NCIt concept]
- Postmarketing Surveillance [NCIt concept]
- Preclinical Study [NCIt concept]
- Prevalence [NCIt concept]
- Primary Endpoint [NCIt concept]
- Probability [NCIt concept]
- Progression-free Survival [NCIt concept]
- Prospective Study [NCIt concept]
- Protocol Agent [NCIt concept]
- Protocol Treatment Arm [NCIt concept]
- Proxy [NCIt concept]
- Pseudonymization [NCIt concept]
- Quality of Life [NCIt concept]
- Queer [NCIt concept]
- Questionnaire [NCIt concept]
- Randomization [NCIt concept]
- Randomized Controlled Clinical Trial [NCIt concept]
- Real-world Data [NCIt concept]
- Real-world Evidence [NCIt concept]
- Relative Risk [NCIt concept]
- Research Database [NCIt concept]
- Research Hypothesis [NCIt concept]
- Research Repository [NCIt concept]
- Retrospective Study [NCIt concept]
- Risk-Benefit Ratio [NCIt concept]
- Sample Size [NCIt concept]
- Schedule Of Assessments [NCIt concept]
- Secondary Endpoint [NCIt concept]
- Serious Adverse Event [NCIt concept]
- Side Effect [NCIt concept]
- Single Blind Study [NCIt concept]
- Statistical Significance [NCIt concept]
- Study Compensation [NCIt concept]
- Study Conduct [NCIt concept]
- Study Design [NCIt concept]
- Study Feasibility [NCIt concept]
- Study Intervention Tolerability [NCIt concept]
- Study Life Cycle [NCIt concept]
- Study Outcome Description [NCIt concept]
- Study Outcome Measurement [NCIt concept]
- Study Participant [NCIt concept]
- Study Population [NCIt concept]
- Study Registry [NCIt concept]
- Study Results [NCIt concept]
- Study Subject Discontinuation [NCIt concept]
- Subject Noncompliance [NCIt concept]
- Subject Risk [NCIt concept]
- Substudy [NCIt concept]
- Superiority Trial [NCIt concept]
- Synergistic Effect [NCIt concept]
- Temporal Frequency [NCIt concept]
- Titration Study [NCIt concept]
- Transgender Man [NCIt concept]
- Transgender Woman [NCIt concept]
- Treatment Effect [NCIt concept]
- Trial Phase [NCIt concept]
- Trial Screening [NCIt concept]
- Trial Statistician [NCIt concept]
- Umbrella Trial [NCIt concept]
- Voluntary Participation [NCIt concept]
- Washout Period [NCIt concept]
- Withdrawal by Subject [NCIt concept]
- X-Ray Imaging [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients