Rates and determinants of informed consent: A case study of an international thromboprophylaxis trial

Abstract Background Successful completion of randomized trials depends upon efficiently and ethically screening patients and obtaining informed consent. Awareness of modifiable barriers to obtaining consent may inform ongoing and future trials. Objective The objective of this study is to describe an...

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Veröffentlicht in:	Journal of critical care 2013-02, Vol.28 (1), p.28-39
Hauptverfasser:	Smith, Orla M., RN, McDonald, Ellen, RN, Zytaruk, Nicole, RN, Foster, Denise, RN, Matte, Andrea, RRT, Clarke, France, RRT, Meade, Laurie, RN, O'Callaghan, Nicole, BA, Vallance, Shirley, RN, Galt, Pauline, RN, Rajbhandari, Dorrilyn, RN, Rocha, Marcelo, MD, Mehta, Sangeeta, MD, Ferguson, Niall D., MD, Hall, Richard, MD, Fowler, Robert, MD, Burns, Karen, MD, Qushmaq, Ismael, MD, Ostermann, Marlies, MD, Heels-Ansdell, Diane, MSc, Cook, Deborah, MD
Format:	Artikel
Sprache:	eng
Schlagworte:	Clinical research Clinical trials Critical Care Guideline Adherence Humans Informed consent Informed Consent - ethics Intensive care Intensive Care Units Logistic Models Medical research Multivariate Analysis Organizational Case Studies Randomized Controlled Trials as Topic - ethics Randomized trials Studies Thromboembolism - prevention & control Vulnerable Populations
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