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Influence of lack of blinding on the estimation of medication-related harms: a retrospective cohort study of randomized controlled trials.

Chang XuFengying ZhangSuhail A R DoiLuis Furuya-KanamoriLifeng LinHaitao ChuXi YangSheyu LiLiliane ZorzelaSu GolderYoon LokeSunita Vohra
Published in: BMC medicine (2024)
Lack of blinding of participants and health care providers in randomized controlled trials may underestimate medication-related harms. Adequate blinding in randomized trials, when feasible, may help safeguard against potential bias in estimating the effects of harms.
Keyphrases
  • healthcare
  • randomized controlled trial
  • adverse drug
  • emergency department
  • clinical trial
  • study protocol
  • social media
  • drug induced
  • electronic health record
  • meta analyses