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A Comparison of Sustained-release Bupropion and Placebo for Smokeless Tobacco Cessation

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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.
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Document Type: Research Article

Affiliations: 1: Addiction and Psychiatric Medicine Research, Department of Behavioral Medicine & Psychiatry, West Virginia University School of Medicine, Morgantown, WV. 2: Department of Community Medicine, West Virginia University School of Medicine, Morgantown, WV.

Publication date: 2002-09-01

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  • The American Journal of Health Behavior seeks to improve the quality of life through multidisciplinary health efforts in fostering a better understanding of the multidimensional nature of both individuals and social systems as they relate to health behaviors.

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