Placebo-controlled trials and the logic of clinical purpose

IRB. Nov-Dec 1990;12(6):1-6.
No abstract available

MeSH terms

  • Control Groups
  • Deception
  • Drug-Related Side Effects and Adverse Reactions
  • Ethical Analysis
  • Ethics
  • Human Experimentation*
  • Humans
  • Informed Consent
  • Organizational Policy
  • Pharmaceutical Preparations
  • Physicians
  • Placebos*
  • Random Allocation
  • Reference Standards
  • Research Design*
  • Risk
  • Risk Assessment
  • Societies
  • United States Food and Drug Administration

Substances

  • Pharmaceutical Preparations
  • Placebos