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, ...
This review addresses one important hurdle in the conduct of low-risk pRCTs: the need to seek participants' written informed consent, and suggests the EU ...
Oct 22, 2024 · Finally, our finding that few pragmatic RCTs reported using a waiver of consent is in contrast to recent academic writing, and research funding ...
Who is willing to participate in low-risk pragmatic clinical trials without consent? Rafael Dal-Ré. European Journal of Clinical Pharmacology, 2017. download ...
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 ...
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