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.
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Mar 27, 2019 · EU clinical trial regulations should be revised to allow the waiver or modification of informed consent in low risk pragmatic trials. Real ...
“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 ...
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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The current studies used retrospective, anonymised data extracted from medical records without the need for patient consent. This ethical method of data ...
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Low risk pragmatic trials do not always require participants' informed consent. Dal-Ré, Rafael; Avendaño-Solà, Cristina; Bloechl-Daum, Brigitte; De Boer ...
Oct 22, 2024 · ... The need to obtain participants' written informed consent in low-risk pRCTs has been shown that could jeopardize the conduct of these trials ...