Participants’ perceptions and understanding of a malaria clinical trial in Bangladesh

In this study interviews were conducted with adult clinical trial participants in Ramu Upazila Health Complex

Abstract

This paper suggest that using a standard consent form following the current International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Good Clinical Practice guidelines does not achieve fully informed consent. It concludes that the process should be revised, simplified and adapted to individual trial settings.

Citation

Das, D. et al. Participants’ perceptions and understanding of a malaria clinical trial in Bangladesh. Malaria Journal (2014) 13:217

Participants’ perceptions and understanding of a malaria clinical trial in Bangladesh

Help us improve GOV.UK

Don’t include personal or financial information, eg your National Insurance number or credit card details.