Enhancing informed consent in clinical trials and exploring resistances to disclosing adverse clinical trial results
- PMID: 19998159
- PMCID: PMC3717209
- DOI: 10.1080/15265160902948330
Enhancing informed consent in clinical trials and exploring resistances to disclosing adverse clinical trial results
Comment on
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The duty to disclose adverse clinical trial results.Am J Bioeth. 2009 Aug;9(8):24-32. doi: 10.1080/15265160902984988. Am J Bioeth. 2009. PMID: 19998154
References
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- Brendel DH, Miller FG. A plea for pragmatism in clinical research ethics. American Journal of Bioethics. 2008;8(4):24–31. - PubMed
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- Freedman A, Fuks A, Weijer C. Demarcating research and treatment: A systematic approach for the analysis of the ethics of clinical research. Clinical Research. 1992;40:653–660. - PubMed
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- Liao SM, Sheehan M, Clarke S. The duty to disclose adverse clinical trials results. American Journal of Bioethics. 2009;9(8):24–32. - PubMed
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- Miller FG, Brody H. What makes placebo-controlled trials unethical? American Journal of Bioethics. 2002;2:3–9. - PubMed
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