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Mar 27, 2019 · Pragmatic RCTs aim to provide evidence of immediate relevance to the decisions of patients, healthcare professionals, and policy makers.
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.
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Mar 9, 2020 · This review addresses one important hurdle in the conduct of low-risk pRCTs: the need to seek participants' written informed consent.
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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, ...
Clinical trial regulations should remove unnecessary obstacles for the conduct of pragmatic trials assessing the comparative effectiveness of medicines ...
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. Dal-Ré, Rafael; Avendaño-Solà, Cristina; Bloechl-Daum, Brigitte; de Boer ...
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 ...
The current studies used retrospective, anonymised data extracted from medical records without the need for patient consent. This ethical method of data ...
Mar 27, 2019 · Dive into the research topics of 'Low risk pragmatic trials do not always require participants' informed consent'. Together they form a unique ...