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
Links
Participants’ perceptions and understanding of a malaria clinical trial in Bangladesh
Updates to this page
Published 4 June 2014