Clinical Trials Directory

Trials / Completed

CompletedNCT00802412

Topiramate to Aid Smoking Cessation in Alcohol Dependent Men

Topiramate to Aid Smoking Cessation in Recovering Alcohol Dependent Men

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
132 (actual)
Sponsor
VA Office of Research and Development · Federal
Sex
Male
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether topiramate is effective as an aid to smoking cessation for recovering alcohol dependent men.

Detailed description

This study is a 12-week, double-blind, placebo-controlled trial to test the efficacy of topiramate versus placebo as an aid to smoking cessation for recovering alcohol dependent men. Another aim of the study is to explore whether or not topiramate reduces relapse to alcohol use in patients with comorbid alcohol and nicotine dependence. All participants will receive a standardized psychosocial intervention in combination with the medication (or placebo). Following completion of the treatment phase of the study, participants will enter a 24-week follow-up period during which the longer-term outcome of the intervention will be assessed.

Conditions

Interventions

TypeNameDescription
DRUGTopiramateTopiramate will be titrated over 5 weeks to a maximum dosage of 200 mg according to the following schedule: 25mg daily for days 1-7, 50mg daily for days 8-14, 75mg daily for days 15-21, 100mg daily for days 22-28, 150mg daily for days 29-35, 200mg daily for days 36-42. Maximum dosage will be maintained for 6 weeks, followed by a one-week taper-off period (100mg daily for 4 days and 50mg daily for 3 days).
DRUGPlaceboPlacebo/study medication will be administered in opaque capsules in an identical fashion to maintain the double-blind study design.

Timeline

Start date
2009-01-01
Primary completion
2014-11-01
Completion
2015-06-01
First posted
2008-12-04
Last updated
2017-01-31
Results posted
2017-01-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00802412. Inclusion in this directory is not an endorsement.