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GABA (Gamma Amino Butyric Acid) Medication for Tobacco

Primary Purpose

Nicotine Dependence

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
pregabalin
cigarettes
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nicotine Dependence focused on measuring smoking sensations, no cravings, desire to smoke

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Female and male smokers, aged 18 to 55 years
  • History of smoking daily for the past 12 months
  • at least 15 cigarettes daily
  • In good health as verified by medical history
  • screening examination
  • screening laboratory tests
  • not pregnant as determined by pregnancy screening, nor breast feeding
  • using acceptable birth control methods.

Exclusion Criteria:

  • History of pregabalin allergy
  • Use of psychotropic medication antidepressants, antipsychotics DSM-IV axis I diagnosis (schizophrenia, bipolar disorder, major depression
  • Dependence or abuse of alcohol or any other illicit or prescription drugs
  • current use of any other tobacco products, including smokeless tobacco
  • history of seizures
  • Inability to fulfill all scheduled visits and examination procedures

Sites / Locations

  • Yale University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

A

2

Arm Description

pregabalin 300mg/day given in conjunction with smoking cigarettes.

cigarettes given in conjunction with pregabalin

Outcomes

Primary Outcome Measures

We believe this medication will help people to stop smoking

Secondary Outcome Measures

Full Information

First Posted
March 24, 2008
Last Updated
March 31, 2020
Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA), US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT00644137
Brief Title
GABA (Gamma Amino Butyric Acid) Medication for Tobacco
Official Title
Pregabalin Given to Tobacco Users to Study Addiction
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
February 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA), US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to examine the effects of a GABA (gamma amino butyric acid)-enhancing medication, pregabalin (300 mg/day), on smoking behavior, tobacco withdrawal and cigarette craving in smokers. We hypothesize that in smokers, pregabalin at 300 mg/day, will be more effective than placebo in decreasing smoking behavior and attenuating tobacco withdrawal and cigarette craving.
Detailed Description
A total of 40 smokers will be randomly assigned to a sequence of treatment conditions: 300 mg/day pregabalin or placebo treatment. Each treatment condition will last 4 days, separated by 3 to 15 days of washout period. Smokers will have twice daily outpatient visits during the first 3 days and a test session on day 4. In each treatment period, smokers will abstain from smoking for 2.5 days, starting at 10 pm on Day 1 until the test session on Day 4. During the test sessions, measures of smoking behavior and tobacco withdrawal will be obtained. Smoking is an important public health problem costing over 430,000 lives a year in this county alone. The first line-treatments, Nicotine Replacement Treatments (NRT) or bupropion, compared to placebo, approximately double the long-term success rate for smoking cessation. Given that there remains 46 million smokers in this country and over 70 percent of them interested in quitting smoking, development of new treatments for smoking cessation will have great public health implications. Currently this protocol is complete with 24 completers. This study has been published. (April 2011)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nicotine Dependence
Keywords
smoking sensations, no cravings, desire to smoke

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
pregabalin 300mg/day given in conjunction with smoking cigarettes.
Arm Title
2
Arm Type
Experimental
Arm Description
cigarettes given in conjunction with pregabalin
Intervention Type
Drug
Intervention Name(s)
pregabalin
Other Intervention Name(s)
300mg/day for pregabalin with smoking cigarettes
Intervention Description
Help stop smoking
Intervention Type
Other
Intervention Name(s)
cigarettes
Intervention Description
help stop smoking with study medication
Primary Outcome Measure Information:
Title
We believe this medication will help people to stop smoking
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Female and male smokers, aged 18 to 55 years History of smoking daily for the past 12 months at least 15 cigarettes daily In good health as verified by medical history screening examination screening laboratory tests not pregnant as determined by pregnancy screening, nor breast feeding using acceptable birth control methods. Exclusion Criteria: History of pregabalin allergy Use of psychotropic medication antidepressants, antipsychotics DSM-IV axis I diagnosis (schizophrenia, bipolar disorder, major depression Dependence or abuse of alcohol or any other illicit or prescription drugs current use of any other tobacco products, including smokeless tobacco history of seizures Inability to fulfill all scheduled visits and examination procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mehmet Sofuoglu, M.D., Ph.D.
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale University
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06520
Country
United States

12. IPD Sharing Statement

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GABA (Gamma Amino Butyric Acid) Medication for Tobacco

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