Sibutramine in weight control: a dose-ranging, efficacy study

Clin Pharmacol Ther. 1991 Sep;50(3):330-7. doi: 10.1038/clpt.1991.144.

Abstract

We tested the safety and efficacy of sibutramine, 5 and 20 mg, and placebo on weight loss. Medication was added to caloric restriction, behavior modification, and exercise in a parallel-group, double-blind clinical trial. Participants were 130% to 180% of ideal body weight and in good health. The study lasted 12 weeks over Thanksgiving, Christmas, and New Year's Day. Weight loss during 8 weeks of study medication was: placebo, 1.4 +/- 2.1 kg (n = 19); 5 mg sibutramine, 2.9 +/- 2.3 kg (n = 18); and 20 mg sibutramine, 5.0 +/- 2.7 kg (n = 18) (p less than 0.05 sibutramine, 5 and 20 mg, versus placebo; p less than 0.05 sibutramine, 20 mg versus 5 mg). There is a significant dose-effect relationship. Five participants left the study before completion, all because of adverse events; placebo (one patient), 5 mg sibutramine (one patient), and 20 mg sibutramine (three patients). Sleep difficulties were noted by eight participants (20 mg sibutramine, seven patients; 5 mg, one patient; and placebo, no patients). Six of 21 participants receiving 20 mg complained of irritability, unusual impatience, or "excitation." Sibutramine, 5 and 20 mg, added to a multimodal program assisted participants in losing weight.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Behavior Therapy
  • Body Weight / drug effects*
  • Cyclobutanes / adverse effects
  • Cyclobutanes / therapeutic use*
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Drug Evaluation
  • Energy Intake
  • Exercise
  • Humans
  • Middle Aged
  • Obesity / drug therapy*
  • Patient Compliance
  • Random Allocation

Substances

  • Cyclobutanes
  • sibutramine