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Blind (clinical trial terms)

A clinical trial is "blind" if participants are unaware of whether they are in the experimental or control arm of the study; also referred to as masked.

See also:
Clinical trial
Placebo
Placebo-controlled study Baseline
Bias
Blind
Brief Summary
Baseline
Clinical Trial Enrolment
Clinical
Clinical Trial
Cohort
Control Group
Controlled Trial
Diagnostic Trials
Dichotomous Question
Dose-ranging Trial
Double blind Trial
Drop Out
Drug-drug interaction
Effectiveness
Efficacy
Eligibility Criteria
Endpoint
Experimental Drug
Informed Consent
International Clinical Trial Registry Platform (ICTRP)
Methodology
Open label Trial
Phase I Trials
Phase II Trials
Phase III Trials
Phase IV Trials
Placebo
Placebo Effect
Pre-clinical Trials
Prevention Trials
Quality of Life Trials
Randomisation
Randomised Trial
Risk-benefit analysis
Screening Trials
Single-blind Trial
Trial endpoint
Treatment Trials
Adverse Event
Adverse Reaction

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Related terms

Control group, Treatment trials, Safety assessment of marketed medicines studies (SAMM), Brief summary, Prompted recall, New product development (NPD), Single-blind trial, Lifestyle drug, Epidemiology, Empirical, Research and development (R&D), European Union of Medical Specialists (UEMS), Placebo effect, Placebo-controlled trial, Data sheet,

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