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Evaluation of the ability of clinical research participants to comprehend informed consent form
Contemporary Clinical Trials , 08/24/09
Bhansali S et al. – CS of patients in trials conducted in developing countries can be reasonably good if the investigators explain the consent form in simple language to the participants and CS is not related to the educational status of the participants. Moreover, though a larger majority of patients agree to participate after knowing study details, some patients exercise their right to refuse.
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