Testing a drug during labour: the experiences of women who participated in a clinical trial

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    Abstract

    Interviews were conducted with 104 patients who had participated in medical research involving pharmaceutical drugs. All patients were asked about the amount of information they had been given prior to being invited to participate, and about their understanding of, and satisfaction with, that information. Patients were also invited to comment on their reasons for having agreed to take part in medical research. Each had participated in one of 14 different drug studies. One of these studies involved a drug that was being used for the first time during labour When analysing these data, it became apparent to the author that responses from some of those involved in the labour drug study were different from those of patients who had participated in the other studies. This paper compares the views of the 26 patients in the labour study with those of the 78 other patients. The women in the labour trial were generally less satisfied than patients in the comparative sample with the information which they had been given, and reported lower levels of understanding of that information. They had asked fewer questions about their study and reported lower levels of satisfaction with the answers they had received to those questions. This raises concerns as to whether the consent to participation given by women in the labour trial was in all cases fully informed. This in turn suggests the possibility of a gender bias in fulfilling ethical obligations in medical research.
    Original languageEnglish
    Pages (from-to)117-131
    Number of pages15
    JournalJournal of Reproductive and Infant Psychology
    Volume18
    Issue number2
    DOIs
    Publication statusPublished - May 2000

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    Keywords

    • Medical research
    • Drug trials
    • Informed consent

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