Conduct of emergency research in patients unable to give consent—Experiences and perceptions of patients, their consent providing next of kin, and treating physicians following a prehospital resuscitation trial

Author:

Kämäräinen Antti,Silfvast Tom,Saarinen Sini,Virta Janne,Virkkunen Ilkka

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Emergency Nursing,Emergency Medicine

Reference14 articles.

1. Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. Official Journal of the European Communities, http://eur-lex.europa.eu/RECH_naturel.do?ihmlang=en; 2001 [accessed 15.10.10]; L121:34–44.

2. EU harmonises rules for trials;Watson;BMJ,2001

3. Necessary time to achieve next of kin proxy consent for acutely injured altered status patients;Wright;Acad Emerg Med,2001

4. ‘No Time to be Lost!’ Ethical considerations on consent for inclusion in emergency pharmacological research in severe traumatic brain injury in the European Union;Kompanje;Sci Eng Ethics,2007

5. Ethical and legal issues in emergency research: barriers to conducting prospective randomized trials in an emergency setting;Morrison;J Surg Res,2009

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