Report from the panel on the Case for Registers of Clinical Trials at the Eighth Annual Meeting of the Society for Clinical Trials

Control Clin Trials. 1988 Mar;9(1):76-81. doi: 10.1016/0197-2456(88)90010-4.

Abstract

A plenary session at the Eighth Annual Meeting of the Society for Clinical Trials addressed "The Case for Registers of Clinical Trials." There are a number of reasons for having registers of clinical trials: to promote collaboration and communication among investigators regarding new and ongoing clinical trials, to provide a basis for methodologic research, and to facilitate meta-analysis by the availability of a system of trial identification that is independent of the published literature. The experience gleaned by those involved with two existing trial registers, the International Committee on Thrombosis and Haemostasis Registry and the Oxford Database of Perinatal Trials, can be used to provide insight into the issues generic to trial registration. The time perspective to be used, inclusion and exclusion criteria, the practicability of comprehensive prospective registration, and funding are central considerations for these and other registers.

MeSH terms

  • Clinical Trials as Topic*
  • Database Management Systems
  • Female
  • Humans
  • Pregnancy
  • Registries*
  • World Health Organization