A Pilot Clinical Trial of Varenicline as a Treatment for Alcohol Dependence
Primary Purpose
Substance Dependence
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
varenicline
placebo
Sponsored by
About this trial
This is an interventional basic science trial for Substance Dependence
Eligibility Criteria
Inclusion Criteria:
- Age between 21 and 75 years.
- Currently seeking treatment for nicotine dependence (smoke at least 10 cigarettes daily) and found to have problem drinking, alcohol abuse or alcohol dependence (non-physiological) as determined by amount of alcohol consumed weekly (Average weekly alcohol consumption (last 30 days), >7 standard drinks (for women) or >14 standard drinks (for men), clinical interview, and AUDIT score > 8.
- Generally healthy, without serious or unstable medical/mental illness(es).
- Smokers only will be included (degree of nicotine dependence will be assessed and included in analysis).
- Able to give voluntary, written, informed consent
Exclusion Criteria:
- More than 30 days of abstinence from alcohol in the prior 90 days.
- History of major alcohol-related complications within the preceding 2 years (liver failure/cirrhosis, pancreatitis, esophageal varices, liver function tests > 3 X ULN).
- Intolerance to the study medication.
- Current psychiatric disorder(s) requiring clinical treatment.
- Any recent history (i.e. within the preceding 5 years) of suicide attempt or current suicidal ideation.
- Use of illicit or non-prescribed psychotropic drug use (opiates, benzodiazepines, cocaine, PCP, methamphetamine, cocaine, or marijuana more than twice a week).
- A history of complicated alcohol or other drug withdrawal syndrome(s), e.g.: delirium tremens or seizures.
Sites / Locations
- UCSF: Ernest Gallo Clinic and Research Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
varenicline
placebo
Arm Description
Drug: varenicline (Chantix) 12 weeks of oral tablet treatment in an escalating dosing regimen (0.5 mg 1x daily, days 1-3; 0.5mg 2x daily, days 4-7, 1.0 mg 2x daily, days 8-84).
Drug: placebo for varenicline 12 weeks of oral tablet treatment in an escalating dosing regimen (1 - 2x daily).
Outcomes
Primary Outcome Measures
Average Number of Cigarettes Smoked Between the Varenicline and Placebo Groups for Completers Through Week 12.
Secondary Outcome Measures
Average Number of Alcoholic Drinks Consumed Between the Varenicline and Placebo Groups for Completers of the Study Through Week 12.
Alcohol Craving as Measured by the Obsessive Compulsive Drinking Scale (OCDS) Between Varenicline and Placebo Groups for Completers of the Study.
Higher scores on the OCDS indicate increased craving. OCDS possible score range = 0 - 40. Difference in average OCDS scores from week 1 to week 12 were reported for the varenicline and placebo groups in subjects that completed the study.
Full Information
NCT ID
NCT01011907
First Posted
November 9, 2009
Last Updated
February 22, 2013
Sponsor
University of California, San Francisco
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
1. Study Identification
Unique Protocol Identification Number
NCT01011907
Brief Title
A Pilot Clinical Trial of Varenicline as a Treatment for Alcohol Dependence
Official Title
Characterizing Alpha5 Nicotinic Receptors in Alcohol and Nicotine Dependence
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
June 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Purpose: This is an outpatient, randomized, double-blinded, placebo-controlled study in which either varenicline (twice daily) or placebo will be administered over a 12 week study period to examine genetic influences on treatment response to varenicline for reduction of hazardous drinking.
Detailed Description
Hazardous alcohol use and alcohol use disorders (AUDs) are an area of large unmet medical needs. Although there has been some progress with pharmacotherapy for alcohol-dependent individuals, a critical need for the development of novel and additional therapeutic approaches remains. Pharmacotherapy development for AUDs as a therapeutic area has had several recent advancements, where clinically as well as commercially successful additions to available treatment options are available and several more are expected in the near future. Based on recent preclinical work, we believe that varenicline has potential to become one of the first among those newly evolving treatments.
In this study, participants with nicotine dependence will receive standard varenicline or placebo treatment over the recommended course of 12 weeks. Since our research question addresses whether alcohol drinking also diminishes with varenicline treatment, we will not ask participants to alter alcohol use; we will simply follow their use over time. Study visits will take place at the Ernest Gallo Clinic and Research Center. The procedures to be completed include vital signs, blood samples at screening and end of study, urine toxicology screening and the completion of standard questionnaires. No special facilities are required for these procedures. Group therapy (which is not a research procedure, but part of standard nicotine dependence treatment) will take place at the Gallo Center.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance Dependence
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
99 (Actual)
8. Arms, Groups, and Interventions
Arm Title
varenicline
Arm Type
Experimental
Arm Description
Drug: varenicline (Chantix) 12 weeks of oral tablet treatment in an escalating dosing regimen (0.5 mg 1x daily, days 1-3; 0.5mg 2x daily, days 4-7, 1.0 mg 2x daily, days 8-84).
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
Drug: placebo for varenicline 12 weeks of oral tablet treatment in an escalating dosing regimen (1 - 2x daily).
Intervention Type
Drug
Intervention Name(s)
varenicline
Other Intervention Name(s)
Chantix
Intervention Description
12 weeks of oral tablet treatment in an escalating dosing regimen (0.5 mg 1x daily, days 1-3; 0.5mg 2x daily, days 4-7, 1.0 mg 2x daily, days 8-84).
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
12 weeks of oral tablet treatment in an escalating dosing regimen (1 - 2x daily).
Primary Outcome Measure Information:
Title
Average Number of Cigarettes Smoked Between the Varenicline and Placebo Groups for Completers Through Week 12.
Time Frame
Weeks 1-12
Secondary Outcome Measure Information:
Title
Average Number of Alcoholic Drinks Consumed Between the Varenicline and Placebo Groups for Completers of the Study Through Week 12.
Time Frame
Weeks 1-12
Title
Alcohol Craving as Measured by the Obsessive Compulsive Drinking Scale (OCDS) Between Varenicline and Placebo Groups for Completers of the Study.
Description
Higher scores on the OCDS indicate increased craving. OCDS possible score range = 0 - 40. Difference in average OCDS scores from week 1 to week 12 were reported for the varenicline and placebo groups in subjects that completed the study.
Time Frame
Week 1 to Week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age between 21 and 75 years.
Currently seeking treatment for nicotine dependence (smoke at least 10 cigarettes daily) and found to have problem drinking, alcohol abuse or alcohol dependence (non-physiological) as determined by amount of alcohol consumed weekly (Average weekly alcohol consumption (last 30 days), >7 standard drinks (for women) or >14 standard drinks (for men), clinical interview, and AUDIT score > 8.
Generally healthy, without serious or unstable medical/mental illness(es).
Smokers only will be included (degree of nicotine dependence will be assessed and included in analysis).
Able to give voluntary, written, informed consent
Exclusion Criteria:
More than 30 days of abstinence from alcohol in the prior 90 days.
History of major alcohol-related complications within the preceding 2 years (liver failure/cirrhosis, pancreatitis, esophageal varices, liver function tests > 3 X ULN).
Intolerance to the study medication.
Current psychiatric disorder(s) requiring clinical treatment.
Any recent history (i.e. within the preceding 5 years) of suicide attempt or current suicidal ideation.
Use of illicit or non-prescribed psychotropic drug use (opiates, benzodiazepines, cocaine, PCP, methamphetamine, cocaine, or marijuana more than twice a week).
A history of complicated alcohol or other drug withdrawal syndrome(s), e.g.: delirium tremens or seizures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Howard Fields, MD PhD
Organizational Affiliation
UCSF: Ernest Gallo CLinic and Research Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jennifer Mitchell, PhD
Organizational Affiliation
UCSF: Ernest Gallo Clinic and Research Center
Official's Role
Study Director
Facility Information:
Facility Name
UCSF: Ernest Gallo Clinic and Research Center
City
Emeryville
State/Province
California
ZIP/Postal Code
94608
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
22547331
Citation
Mitchell JM, Teague CH, Kayser AS, Bartlett SE, Fields HL. Varenicline decreases alcohol consumption in heavy-drinking smokers. Psychopharmacology (Berl). 2012 Oct;223(3):299-306. doi: 10.1007/s00213-012-2717-x. Epub 2012 May 1.
Results Reference
result
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A Pilot Clinical Trial of Varenicline as a Treatment for Alcohol Dependence
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