The role of an initial single-blind placebo period in phase I clinical trials

Fundam Clin Pharmacol. 1994;8(2):185-7. doi: 10.1111/j.1472-8206.1994.tb00796.x.

Abstract

The effect of an initial single-blind placebo period in a phase I clinical trial was assessed in 12 volunteers who underwent five weekly treatment periods, consisting of treatment on the first day and a six-day wash-out period. An initial single-blind placebo period was followed by three different single doses of a platelet-aggregation factor inhibitor and another placebo period, under a double-blind Latin square design. Reports of abnormal symptoms were collected using a questionnaire designed by our group. A total of 13 abnormal symptoms were reported during the first period and only nine for the following four periods, indicating a clear placebo period effect. These preliminary results suggest that an initial single-blind period may be usefully included in phase I clinical trials.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I
  • Randomized Controlled Trial

MeSH terms

  • Clinical Trials, Phase I as Topic / methods*
  • Double-Blind Method
  • Humans
  • Male
  • Placebo Effect*
  • Platelet Activating Factor / antagonists & inhibitors*
  • Platelet Aggregation Inhibitors / adverse effects
  • Single-Blind Method
  • Surveys and Questionnaires

Substances

  • Platelet Activating Factor
  • Platelet Aggregation Inhibitors