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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01621022
Other study ID # IRB S-01-07
Secondary ID
Status Completed
Phase Phase 4
First received June 13, 2012
Last updated December 5, 2016
Start date January 2001
Est. completion date October 2002

Study information

Verified date December 2016
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Focus of this study was to determine if bupropion was more effective for smoking cessation when used alone or combined with nicotine gum.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
bupropion + nicotine gum
150 mg bupropion twice daily plus 4 mg nicotine gum as needed (up to 12 pcs/day)
Active bupropion-Placebo gum
150mg bupropion twice daily plus placebo nicotine gum as needed (up to 12 pcs/day)
Placebo bupropion-Placebo gum
Placebo bupropion twice daily + placebo nicotine gum as needed (up to 12 pcs/day)

Locations

Country Name City State
United States UW Center for Tobacco Research and Intervention Madison Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
University of Wisconsin, Madison National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

References & Publications (1)

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

Outcome

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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