Mar 27, 2019 · Low risk pragmatic trials do not always require participants' informed consent. BMJ. 2019 Mar 27:364:l1092.
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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Nov 15, 2021 · Low risk pragmatic trials do not always require participants' informed consent. BMJ 2019;364(March):l1092 doi: 10.1136/bmj.l1092. [PubMed] ...
Clinical trial regulations should remove unnecessary obstacles for the conduct of pragmatic trials assessing the comparative effectiveness of medicines ...
Jul 3, 2024 · ... The need to obtain participants' written informed consent in low-risk pRCTs has been shown that could jeopardize the conduct of these trials ...
Low risk pragmatic trials do not always require participants' informed consent. Dal-Ré, Rafael; Avendaño-Solà, Cristina; Bloechl-Daum, Brigitte; de Boer ...
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 ...
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Low risk pragmatic trials do not always require participants' informed consent ... consent for clinical investigations involving no more than minimal risk ...
Low risk pragmatic trials do not always require participants' informed consent. Rafael Dal-Ré, Cristina Avendaño-Solà, Brigitte Bloechl-Daum, Anthonius de ...