Clinical Trials Directory

Trials / Completed

CompletedNCT00108537

Non-Nicotine Agents for Smoking Cessation

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
Sponsor
US Department of Veterans Affairs · Federal
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to determine which is the better approach to smoking cessation in veterans: bupropion combined with transdermal nicotine or high dose nicotine replacement therapy (NRT) using transdermal nicotine combined with nicotine inhaler.

Detailed description

This study is a two-arm open-label, randomized controlled trial of bupropion combined with transdermal nicotine versus high dose NRT (transdermal nicotine and nicotine inhaler) with all subjects receiving a behavioral counseling program for smoking cessation.

Conditions

Interventions

TypeNameDescription
DRUGbupropion and transdermal patch
DRUGtransdermal patch and nicotine inhaler

Timeline

Start date
2003-10-01
Completion
2005-09-01
First posted
2005-04-18
Last updated
2008-04-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00108537. Inclusion in this directory is not an endorsement.

Non-Nicotine Agents for Smoking Cessation (NCT00108537) · Clinical Trials Directory