Clinical Trials Directory

Trials / Completed

CompletedNCT01330030

Selegiline Patch for Treatment of Nicotine Dependence

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
243 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

Relapse to smoking is a common problem affecting smokers who seek treatment. The purpose of this study is examine whether selegiline, given in the form of a skin patch, is effective in stopping smoking.

Detailed description

Most smokers relapse following smoking cessation treatment. More effective smoking cessation therapies are needed to prevent the high rates of relapse. Selegiline is a selective inhibitor of monoamine oxidase B (MAO B) and has been used clinically in combination with levodopa to treat Parkinson's disease. Selegiline permits the stabilization of dopamine (DA) levels in the brain by preventing the rapid degradation of DA by means of MAO B and is used as an adjunct to levodopa therapy causing a dose-sparing effect and enhancing dopaminergic transmission. Selegiline's effect on MAO B and the resulting effect on brain DA has interesting implications for the treatment of nicotine dependence because brain DA systems may play a key role in the mediation of reward learning behavior. Previous research suggests that the brains of living smokers show a 40% decrease in the level of MAO B relative to nonsmokers or former smokers. The purpose of this study is examine whether selegiline, administered in the form of a skin patch, is effective for smoking cessation. Participants will be randomly assigned to one of two treatments: 1) transdermal selegiline patch (STS) or 2) placebo. Treatment with STS or placebo will be given for a period of 8 weeks. Participants will be stratified by gender to evaluate the role that gender plays in moderating smoking cessation treatment. Study visits will take place once each week for 30 to 45 minutes, and will include adverse events monitoring, biochemical verification of smoking status, and a physical exam. Follow-up visits will occur at Weeks 24 and 52 to determine response to treatment.

Conditions

Interventions

TypeNameDescription
DRUGSelegiline6mg/24 hrs for 8 weeks
OTHERmatching placeboplacebo/24hrs for 8 weeks

Timeline

Start date
2005-07-01
Primary completion
2008-08-01
Completion
2011-07-01
First posted
2011-04-06
Last updated
2016-08-10
Results posted
2016-04-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01330030. Inclusion in this directory is not an endorsement.