Journal article
Low risk pragmatic trials do not always require participants' informed consent
R Dal-Ré, C Avendaño-Solà, B Bloechl-Daum, A De Boer, S Eriksson, U Fuhr, S Holm, SK James, RJ Mentz, E Perucca, FR Rosendaal, S Treweek
BMJ | BMJ PUBLISHING GROUP | Published : 2019
DOI: 10.1136/bmj.l1092
Abstract
Clinical trial regulations should remove unnecessary obstacles for the conduct of pragmatic trials assessing the comparative effectiveness of medicines posing no or minimal risk to participants, say Rafael Dal-Ré and colleagues