A comparison of sustained-release bupropion and placebo for smokeless tobacco cessation

Am J Health Behav. 2002 Sep-Oct;26(5):386-93. doi: 10.5993/ajhb.26.5.7.

Abstract

Objective: To evaluate the potential efficacy of bupropion sustained release when used in combination with minimal counseling for moist snuff cessation in males.

Methods: A double-blind, placebo-controlled 3-month trial. The active treatment group (n = 35) received bupropion SR at 150 mg/qd day for the first 3 days, then beginning day 4 through day 49 (7 weeks) 150 mg/ b.i.d. The placebo group (n= 35) received 1 tablet qd for 3 days and beginning day 4 through day 49, 1 tablet/b.i.d.

Results: Bupropion 300 mg/day (150 b.i.d.) produced significantly higher quit rates for smokeless tobacco cessation at the end of treatment (7 weeks) than placebo (p = 0.04) with an OR of 2.73.

Conclusion: Bupropion SR appears to be effective for smokeless tobacco cessation.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Bupropion / administration & dosage*
  • Bupropion / adverse effects
  • Delayed-Action Preparations
  • Dopamine Uptake Inhibitors / administration & dosage*
  • Dopamine Uptake Inhibitors / adverse effects
  • Double-Blind Method
  • Humans
  • Male
  • Middle Aged
  • Motivation
  • Placebos
  • Tobacco Use Disorder / drug therapy*
  • Tobacco Use Disorder / prevention & control
  • Tobacco, Smokeless*
  • Treatment Outcome

Substances

  • Delayed-Action Preparations
  • Dopamine Uptake Inhibitors
  • Placebos
  • Bupropion