In this study interviews were conducted with adult clinical trial participants in Ramu Upazila Health Complex
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.
Das, D. et al. Participants’ perceptions and understanding of a malaria clinical trial in Bangladesh. Malaria Journal (2014) 13:217