Mar 27, 2019 · Low risk pragmatic trials do not always require participants' informed consent. BMJ. 2019 Mar 27:364:l1092. doi: 10.1136/bmj.l1092. Authors.
Mar 27, 2019 · Pragmatic RCTs aim to provide evidence of immediate relevance to the decisions of patients, healthcare professionals, and policy makers.
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“Low risk pragmatic trials do not always require participants' informed consent.” BMJ 364 (March 27, 2019): l1092. https://doi.org/10.1136/bmj.l1092. Dal-Ré R, ...
Low risk pragmatic trials do not always require participants' informed consent. Dal-Ré, Rafael; Avendaño-Solà, Cristina; Bloechl-Daum, Brigitte; de Boer ...
Clinical trial regulations should remove unnecessary obstacles for the conduct of pragmatic trials assessing the comparative effectiveness of medicines ...
Jul 3, 2024 · 6, 7,33 Waivers of consent may be granted when risks to study participants are minimal, when the research has important social value, and where ...
However, these trials may be undermined by the requirement to obtain written informed consent, which can decrease accrual and increase selection bias. Recent ...
Low risk pragmatic trials do not always require participants' informed consent. Dal-Ré, Rafael; Avendaño-Solà, Cristina; Bloechl-Daum, Brigitte; De Boer ...
Low risk pragmatic trials do not always require participants' informed consent. Clinical trial regulations should remove unnecessary obstacles for the ...
Low risk pragmatic trials do not always require participants' informed consent · University of Melbourne Researchers · Grants · Citation metrics · Keywords.