Tobacco Dependence Clinical Trial
Official title:
Efficacy of Bupropion Alone and in Combination With Nicotine Gum
Focus of this study was to determine if bupropion was more effective for smoking cessation when used alone or combined with nicotine gum.
Status | Completed |
Enrollment | 608 |
Est. completion date | October 2002 |
Est. primary completion date | October 2002 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Smoke 10 or more cigarettes per day - Motivated to quit - No physical or mental health issues that would prevent participation - Not pregnant or willing to prevent pregnancy during treatment Exclusion Criteria: - Carbon monoxide (CO) breath test score below 10 parts per million (ppm) - Center for Epidemiologic Studies Depression Scale (CES-D) score greater than 16 - Heavy alcohol use - History of eating disorder - Suicidality |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | UW Center for Tobacco Research and Intervention | Madison | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
University of Wisconsin, Madison | National Institutes of Health (NIH) |
United States,
Piper ME, Federman EB, McCarthy DE, Bolt DM, Smith SS, Fiore MC, Baker TB. Efficacy of bupropion alone and in combination with nicotine gum. Nicotine Tob Res. 2007 Sep;9(9):947-54. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 7-day point prevalence abstinence measured at 6 months | No smoking, not evan a puff, during the 7 days prior to the 6 month follow-up | 6 months | No |
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