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ABSTRACT: Objectives
Randomised trials for the management of drug-resistant infections are challenging to conduct as target patient populations often lack decision-making capacity, and enrolment windows are typically short. Improving informed consent and risk communication in these trials is especially crucial for protecting patient interests and maximising trial efficiency. This study aimed to understand challenges in risk communication and informed consent in antimicrobial clinical trials.Design
Scoping review.Data sources
Searches were conducted in Embase, Medline, CINAHL and Web of Science Core for peer-reviewed English articles that were published from January 2000 to April 2023.Eligibility criteria
Included articles were empirical studies or expert opinions that
SUBMITTER: Shou Y
PROVIDER: S-EPMC11590817 | biostudies-literature | 2024 Nov
REPOSITORIES: biostudies-literature