Ancillary-care responsibilities in observational research: two cases, two issues

dc.contributor.authorMutabingwa, Theonest K.
dc.date.accessioned2020-10-08T07:15:17Z
dc.date.available2020-10-08T07:15:17Z
dc.date.issued2007
dc.description.abstractInternational collaborative research in developing countries raises difficult ethical issues in the setting of severe diseases and complex costly treatments. Discussion of two matters has characterized the debate on this type of research. First, what standard of care should be provided to participants in intervention studies, particularly those in control groups? 1,2,3,4 Second, what level of benefits should be provided to individuals and communities during a study and after completion, particularly with respect to treatments proven effective through research? 4, 5, 6 Here, we focus on a third issue, investigators' responsibilities for meeting participants' needs for ancillary care.en_US
dc.identifier.citationDickert, N., DeRiemer, K., Duffy, P.E., Garcia-Garcia, L., Mutabingwa, T.K., Sina, B.J., Tindana, P. and Lie, R., 2007. Ancillary-care responsibilities in observational research: two cases, two issues. The Lancet, 369(9564), pp.874-877.en_US
dc.identifier.otherDOI:https://doi.org/10.1016/S0140-6736(07)60416-4
dc.identifier.urihttp://hdl.handle.net/123456789/620
dc.language.isoenen_US
dc.publisherThe Lanceten_US
dc.subjectResearch methodologyen_US
dc.subjectEthical issuesen_US
dc.subjectDiseaseen_US
dc.titleAncillary-care responsibilities in observational research: two cases, two issuesen_US
dc.typeArticleen_US

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