Relief of epigastric pain in nonulcer dyspepsia: controlled trial of the promotility drug cisapride

Clin Ther. 1989;11(1):62-8.

Abstract

In a randomized, double-blind, placebo-controlled study, 32 patients with nonulcer dyspepsia received 5 mg of cisapride or placebo three times daily for four weeks after a two-week run-in phase on placebo. Limited antacid use was allowed. Cisapride was superior to placebo in reducing the intensity of epigastric pain at two weeks (P = 0.03) and four weeks (P = 0.01). At the end of treatment, 82% of the cisapride-treated patients and 43% of the controls had no or only mild pain. Minor, gastrointestinal side effects were observed in two cisapride-treated patients and in one control.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Antacids / administration & dosage
  • Antacids / therapeutic use
  • Cisapride
  • Clinical Trials as Topic
  • Double-Blind Method
  • Dyspepsia / complications
  • Dyspepsia / drug therapy*
  • Female
  • Humans
  • Male
  • Pain / drug therapy*
  • Pain / etiology
  • Piperidines / therapeutic use*
  • Random Allocation
  • Serotonin Antagonists / therapeutic use*
  • Time Factors

Substances

  • Antacids
  • Piperidines
  • Serotonin Antagonists
  • Cisapride