The CIOMS view on the use of placebo in clinical trials

Sci Eng Ethics. 2004 Jan;10(1):23-8. doi: 10.1007/s11948-004-0058-9.

Abstract

Based on worldwide consultations with experts in science and ethics the revised CIOMS 2002 International Ethical Guidelines for Biomedical Research Involving Human Subjects provide guidance on when the use of placebo as a comparator in clinical research is ethically acceptable. The article reviews the main points of the CIOMS Guidelines and commentaries including the use of placebo in situations where the best current method is available and the relation of placebo to established effective intervention. It discusses the use of placebo in externally sponsored research in low-resource countries and requirements for informed consent related to placebo studies.

MeSH terms

  • Europe
  • Guidelines as Topic*
  • Human Experimentation / ethics*
  • Human Experimentation / standards
  • Humans
  • Informed Consent / ethics
  • Informed Consent / standards
  • International Agencies
  • International Cooperation
  • Moral Obligations
  • Placebos*
  • Research Subjects

Substances

  • Placebos