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Clinical Trials/NCT00063323
NCT00063323
Completed
Phase 3

Maintenance Treatment for Prevention of Smoking Relapse

National Institute on Drug Abuse (NIDA)1 site in 1 country589 target enrollmentAugust 2000
InterventionsBupropion

Overview

Phase
Phase 3
Intervention
Bupropion
Conditions
Tobacco Use Disorder
Sponsor
National Institute on Drug Abuse (NIDA)
Enrollment
589
Locations
1
Primary Endpoint
Survival abstinence rate with maintenance treatment
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to determine the efficacy and cost-effectiveness of long-term pharmacotherapy (using Zyban and/or nicotine replacement) for reducing the relapse rate associated with stopping smoking.

Detailed Description

The goal of this study was to assess relapse prevention outcomes among individuals able to stop smoking when pharmacotherapy is extended beyond the standard duration of treatment. We hypothesized that maintenance treatment with prolonged bupropion use and/or "as needed" use of nicotine gum will reduce relapse to smoking. Participants were recruited through advertisements on radio, television, newspapers, the Internet, and various community outlets. Respondents were pre-screened by telephone using a standard interview. The first participant entered the OLT phase in February 2001; the final NTFU visit took place in October 2005. The study was multi-phased consisting of: 1) eight-week open-label treatment (OLT) with bupropion and nicotine patch; 2) randomized double-blind assignment of OLT successes to 16 weeks of placebo-controlled maintenance treatment (MT); and 3) 24 weeks of non-treatment follow-up (NTFU). Participants received $25 compensation for completing the NTFU visits at Weeks 36 and 48. The Institutional Review Board of the New York State Psychiatric Institute approved the study. The study was performed at the Columbia University Medical Center Smoking Cessation Clinic in New York City.

Registry
clinicaltrials.gov
Start Date
August 2000
End Date
July 2006
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients who smoke at least 10 cigarettes daily and have attempted to quit smoking at least once

Exclusion Criteria

  • Seizure History
  • Unstable Blood Pressure
  • Current major depression
  • Current alcohol/drug abuse or dependency
  • Lifetime psychotic illness
  • Current use of psychotropic drugs
  • Unstable medical condition

Arms & Interventions

Bupropion

Bupropion (brand name Zyban Sustained Release). Participants used bupropion SR 150 mg twice daily during the 16-week maintenance treatment.

Intervention: Bupropion

Nicotine gum

Nicotine gum (brand name Nicorette) During the maintenance 16-week maintenance treatment phase, participants assigned to this arm received 2 mg. nicotine gum.

Intervention: Bupropion

Bupropion+Nicotine Gum

Combined active treatments: Bupropion (Zyban SR) and nicotine gum (Nicorette). Participants were instructed to use the 150 mg bupropion pill twice daily and the 2 mg. gum as needed during the 16-week maintenance treatment phase.

Intervention: Bupropion

Double placebo

Placebo gum + placebo pill. Identical placebo pill was used twice daily and identical placebo gum was used as needed.

Intervention: Bupropion

Outcomes

Primary Outcomes

Survival abstinence rate with maintenance treatment

Time Frame: 48 weeks after start of treatment

Study Sites (1)

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