Consent to open label extension studies: some ethical issues

Wainwright, Paul (2002) Consent to open label extension studies: some ethical issues. Journal of Medical Ethics, 28(6), pp. 373-376. ISSN (print) 0306-6800

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A frequent feature of pharmaceutical research is the open label extension study, in which patients participating in double blind placebo controlled trials of new medications are invited, on completion of the initial trial, to take the study drug for some further period. Patients are openly given the active substance at this stage, regardless of their assignment in the initial trial. Investigators are typically reluctant to unblind the patients’ assignment at the point of entry into the open label phase, on the grounds that this may introduce ascertainment bias in the main study. It is argued that patients invited to participate in open label extension studies cannot give a proper consent to such research unless they know to which arm of the main trial they were recruited. It is further argued that to recruit certain groups of patients from placebo controlled trials into open label extension studies may also be unethical for clinical reasons.

Item Type: Article
Uncontrolled Keywords: Ethics, research ethics, open label extension studies, consent
Research Area: Nursing and midwifery
Faculty, School or Research Centre: Faculty of Health and Social Care Sciences (until 2013)
Depositing User: Paul Wainwright
Date Deposited: 15 May 2007
Last Modified: 16 Jul 2012 21:47

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