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Selegiline Patch for Treatment of Nicotine Dependence

Primary Purpose

Tobacco Use Disorder

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Selegiline
matching placebo
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tobacco Use Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts 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

Sites / Locations

  • Stanford University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Drug Selegiline

Matching placebo

Arm Description

6 mg selegiline patch (transdermal) worn for 24 hours for 8 weeks

matching placebo worn 24 hours for 8 weeks

Outcomes

Primary Outcome Measures

Expired-air Carbon Monoxide Confirmed Smoking Abstinence
expired-air carbon monoxide confirmed smoking abstinence at 52 weeks

Secondary Outcome Measures

Full Information

First Posted
November 8, 2010
Last Updated
June 29, 2016
Sponsor
Stanford University
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01330030
Brief Title
Selegiline Patch for Treatment of Nicotine Dependence
Official Title
Selegiline Patch for Treatment of Nicotine Dependence
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
243 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Drug Selegiline
Arm Type
Experimental
Arm Description
6 mg selegiline patch (transdermal) worn for 24 hours for 8 weeks
Arm Title
Matching placebo
Arm Type
Placebo Comparator
Arm Description
matching placebo worn 24 hours for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Selegiline
Other Intervention Name(s)
EMSAM
Intervention Description
6mg/24 hrs for 8 weeks
Intervention Type
Other
Intervention Name(s)
matching placebo
Other Intervention Name(s)
Placebo
Intervention Description
placebo/24hrs for 8 weeks
Primary Outcome Measure Information:
Title
Expired-air Carbon Monoxide Confirmed Smoking Abstinence
Description
expired-air carbon monoxide confirmed smoking abstinence at 52 weeks
Time Frame
52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joel D Killen
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20707784
Citation
Killen JD, Fortmann SP, Murphy GM Jr, Hayward C, Fong D, Lowenthal K, Bryson SW, Killen DT, Schatzberg AF. Failure to improve cigarette smoking abstinence with transdermal selegiline + cognitive behavior therapy. Addiction. 2010 Sep;105(9):1660-8. doi: 10.1111/j.1360-0443.2010.03020.x.
Results Reference
result

Learn more about this trial

Selegiline Patch for Treatment of Nicotine Dependence

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