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PDFClinical ethics
Improving the quality of consent to randomised controlled trials by using continuous consent and clinician training in the consent process
- Correspondence to: Dr Peter Allmark Northern General Hospital, University of Sheffield, Samuel Fox House, Herries Road, Sheffield S5 7AU, UK; p.j.allmark{at}shef.ac.uk
Citation
Improving the quality of consent to randomised controlled trials by using continuous consent and clinician training in the consent process
Publication history
- Received July 25, 2005
- Accepted October 14, 2005
- Revised October 12, 2005
- First published July 28, 2006.
Online issue publication
July 28, 2006
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Copyright information
Copyright 2006 by the Journal of Medical Ethics
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