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首页> Trials> Coerced consent in clinical research: study protocol for a randomized controlled trial.

Coerced consent in clinical research: study protocol for a randomized controlled trial.

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作者： Connor T A,Brenna ^[1] ; Nancy,Walton ^[2] ; Melanie,Cohn ^[3] ; Urooj,Siddiqui ^[4] ; Ella,Huszti ^[5] ; Richard,Brull ^[6]

作者单位： Department of Anesthesiology & Pain Medicine, University of Toronto, Toronto, ON, Canada. connor.brenna@mail.utoronto.ca. ^[1] Department of Physiology, University of Toronto, Toronto, ON, Canada. connor.brenna@mail.utoronto.ca. ^[2] Yeates School of Graduate Studies, Toronto Metropolitan University, Toronto, ON, Canada. ^[3] Krembil Brain Institute, University Health Network, Toronto, ON, Canada. ^[4] Department of Anesthesiology and Pain Medicine, Mount Sinai Hospital, Toronto, ON, Canada. ^[5] Biostatistics Department, University Health Network, Toronto, ON, Canada. ^[6] Department of Anesthesia and Pain Management, University Health Network, Toronto, ON, Canada. richard.brull@uhn.ca. ^[7] Department of Anesthesia, Women's College Hospital, Toronto, ON, Canada. richard.brull@uhn.ca. ^[8]

关键词 Clinical trials Coercion Perioperative research Research consent Voluntariness

主题词人类(Humans);知情同意(Informed Consent);前瞻性研究(Prospective Studies);随机对照试验(主题)(Randomized Controlled Trials as Topic);病人遴选(Patient Selection);研究对象(Research Subjects);时间因素(Time Factors);女(雌)性(Female);麻醉, 全身(Anesthesia, General)

DOI 10.1186/s13063-024-08294-4

PMID 38965542

发布时间 2024-07-07

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Trials

Trials

2024年25卷1期

452页

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