Research and informed consent in africa — another look

Carel B. Ijsselmuiden, Ruth R. Faden

Research output: Contribution to journalEditorialpeer-review

98 Scopus citations

Abstract

The current practice of requiring the informed consent of research subjects is relatively new. The emphasis on a person's right to accept or refuse participation in biomedical research stems directly from the atrocities committed by Nazi “scientists” — an extreme instance of ignoring the value of individual human beings allegedly in the pursuit of knowledge.1 2 3 Similar but less dramatic disrespect for the subjects of medical research was common just after the Second World War and reflected the paternalistic atmosphere that pervaded medical practice at that time.1,4 More recent examples of unethical research, which stimulated the development of the current theory.

Original languageEnglish (US)
Pages (from-to)830-834
Number of pages5
JournalNew England Journal of Medicine
Volume326
Issue number12
DOIs
StatePublished - Mar 19 1992

ASJC Scopus subject areas

  • General Medicine

Fingerprint

Dive into the research topics of 'Research and informed consent in africa — another look'. Together they form a unique fingerprint.

Cite this