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Open-label trial

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(Redirected from Open-label) Research study in which both the researcher and the participant know which treatment is being used

An open-label trial, or open trial, is a type of clinical trial in which information is not withheld from trial participants. In particular, both the researchers and participants know which treatment is being administered. This contrasts with a double-blinded trial, where information is withheld both from the researchers and the participants to reduce bias.

Open-label trials may be appropriate for comparing two similar treatments to determine which is most effective, such as a comparison of different prescription anticoagulants, or possible relief from symptoms of some disorders when a placebo is given.

An open-label trial may still be randomized. Open-label trials may also be uncontrolled (without a placebo group), with all participants receiving the same treatment.

References

  1. ^ "Open label study". National Cancer Institute, US National Institutes of Health. 2020. Retrieved 20 November 2020.
  2. "Double-blind (trial)". Merriam-Webster Medical Dictionary. 2020. Retrieved 20 November 2020.
  3. "Double-blind study". HIV.gov, Office of AIDS Research, US National Institutes of Health. 2020. Retrieved 20 November 2020.
  4. ^ Beyer-Westendorf, J.; Buller, H. (2011). "External and internal validity of open label or double-blind trials in oral anticoagulation: better, worse or just different?". Journal of Thrombosis and Haemostasis. 9 (11): 2153–2158. doi:10.1111/j.1538-7836.2011.04507.x. ISSN 1538-7933. PMID 21920015.
  5. Ballou, Sarah; Kaptchuk, Ted J.; Hirsch, William; Nee, Judy; Iturrino, Johanna; Hall, Kathryn T.; Kelley, John M.; Cheng, Vivian; Kirsch, Irving; Jacobson, Eric; Conboy, Lisa; Lembo, Anthony; Davis, Roger B. (25 May 2017). "Open-label versus double-blind placebo treatment in irritable bowel syndrome: study protocol for a randomized controlled trial". Trials. 18 (1): 234. doi:10.1186/s13063-017-1964-x. ISSN 1745-6215. PMC 5445390. PMID 28545508.
Clinical research and experimental design
Overview
Controlled study
(EBM I to II-1)
Observational study
(EBM II-2 to II-3)
Measures
OccurrenceIncidence, Cumulative incidence, Prevalence, Point prevalence, Period prevalence
AssociationRisk difference, Number needed to treat, Number needed to harm, Risk ratio, Relative risk reduction, Odds ratio, Hazard ratio
Population impactAttributable fraction among the exposed, Attributable fraction for the population, Preventable fraction among the unexposed, Preventable fraction for the population
OtherClinical endpoint, Virulence, Infectivity, Mortality rate, Morbidity, Case fatality rate, Specificity and sensitivity, Likelihood-ratios, Pre- and post-test probability
Trial/test types
Analysis of clinical trials
Interpretation of results
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