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Selegiline Patch for Treatment of Nicotine Dependence

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Stanford University

Status and phase

Completed
Phase 2

Conditions

Tobacco Use Disorder

Treatments

Drug: Selegiline
Other: matching placebo

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01330030
SU-07232007-459
R01DA017457 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

243 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Smokes greater than 20 cigarettes per day

Exclusion criteria

  • History of Parkinson's disease, high blood pressure, or severe liver or kidney disease
  • Current substance abuse
  • Mental illness
  • Skin conditions that could interfere with patch use
  • Using antidepressant medications (e.g., levodopa/carbidopa, methyldopa, or any MAO inhibitor)
  • Pregnant or breastfeeding

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Quadruple Blind

243 participants in 2 patient groups, including a placebo group

Drug Selegiline
Experimental group
Description:
6 mg selegiline patch (transdermal) worn for 24 hours for 8 weeks
Treatment:
Drug: Selegiline
Matching placebo
Placebo Comparator group
Description:
matching placebo worn 24 hours for 8 weeks
Treatment:
Other: matching placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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