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 VohraPublished 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.