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Treatment With Mecamylamine in Smoking and Non-smoking Alcohol Dependent Patients

Primary Purpose

Alcoholism

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
mecamylamine
Placebo
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcoholism focused on measuring mecamylamine, treatment, alcohol dependence, smoking

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: individuals with DSM-IV diagnosis of alcohol dependence smokers and non-smokers patients who do not require psychotropic medication for the management of their psychiatric symptoms individuals with a history of substance dependence (other than alcohol and tobacco) but have not met criteria for substance dependence in the past 30 days women with acceptable method of contraception Exclusion Criteria: pregnant women medications thought to influence drinking behavior including: acamprosate, disulfiram, naltrexone and ondansetron underlying medical conditions history of glaucoma, prostatic hypertrophy, urethral obstruction, cerebral arteriosclerosis, pyloric stenosis, or a history of hypersensitivity to mecamylamine DSM-IV diagnosis of bipolar disorder, schizophrenia, and schizophrenia-type disorders unstable medical conditions patients who require psychotropic medication for the management of an active psychiatric disorder patients on pharmacological treatment for alcohol and/or nicotine dependence

Sites / Locations

  • VA Connecticut Healthcare System

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

Mecamylamine- Smoker

Placebo-Smoker

Mecamylamine- Non-Smoker

Placebo-Non-Smoker

Arm Description

Outcomes

Primary Outcome Measures

Percent Heavy Drinking Days During Active Treatment Phase
Data were calculated as number of heavy drinking days (heavy drinking days is defined as 5 drinks on a single occasion for men and 4 for women) average during 90 days of treatment.
Self-report Weekly Craving Via Obsessive Compulsive Drinking Scale (OCDS)
The OCDS is a 14-item (rated 0-4), self-administered questionnaire for characterizing and quantifying the obsessive and compulsive cognitive aspects of craving and heavy (alcoholic) drinking, such as drinking-related thought, urges to drink, and the ability to resist those thoughts and urges. A higher total score indicates higher craving and ranges from 0-48.
Self-report Weekly Smoking Craving
Questionnaire of smoking urges (QSU). It has 32 questions that range from 1 to 7, there are 8 questions per sub-scale. The total range is 32 to 224. Each sub-scale ranges from 8- 56, with a higher score indicating higher craving.
Self-report Average Number of Cigarettes Per Day
self-report from only the smoking population for cigarettes per day

Secondary Outcome Measures

Full Information

First Posted
June 19, 2006
Last Updated
May 24, 2019
Sponsor
Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT00342563
Brief Title
Treatment With Mecamylamine in Smoking and Non-smoking Alcohol Dependent Patients
Official Title
Treatment With Mecamylamine in Smoking and Non-smoking Alcohol Dependent Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
May 2004 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study will be to evaluate the efficacy of mecamylamine in reducing alcohol consumption in smoking and non-smoking alcohol dependent patients. We hypothesize that mecamylamine will result in a greater reduction of alcohol consumption than placebo. We further hypothesize that mecamylamine will be effective in reducing both alcohol consumption and smoking in a subset of alcoholics who also smoke.
Detailed Description
RESEARCH PLAN: Although there are two FDA approved medications for the treatment of alcohol dependence (naltrexone and disulfiram), the robust efficacy of both compounds in reducing alcohol consumption has recently been called into question. Given the high rates of alcohol dependence among the general population, development and testing of novel medications is of great importance. Mecamylamine, a noncompetitive NACh receptor antagonist has been shown to be useful in smoking cessation when used in combination with transdermal nicotine. To our knowledge, clinical studies examining the effectiveness of mecamylamine in alcoholism have not been conducted. However, there is evidence from animal research that mecamylamine can block the effects of alcohol. Infusion of mecamylamine into the ventral tegmental area antagonized ethanol-induced dopamine release in rats. More importantly, mecamylamine decreased alcohol intake and preference in alcohol-preferring rats. In two studies with healthy volunteers mecamylamine was effective in attenuating the euphoric effects of alcohol and reducing the craving for alcohol. This is the first study designed to test the clinical efficacy of mecamylamine in a sample of alcohol dependent patients who either do or do not smoke. For the proposed project we will recruit 60 treatment seeking patients between the ages of 18 and 60 who meet criteria for alcohol dependence and may or may not smoke. Patients will be randomized into two groups (30 patients in each group): one dose of mecamylamine (10mg) or placebo in a double-blind fashion for 12 weeks. Patients will be asked to come for follow up 3 months after completing the study. Patients will be excluded if they: take medications thought to influence drinking behavior, have a significant underlying medical conditions, such as cerebral, renal, thyroid, hepatic or cardiac pathology; have a history of glaucoma, prostatic hypertrophy, urethral obstruction, cerebral arteriosclerosis, pyloric stenosis, or a history of hypersensitivity to mecamylamine; or meet current criteria for Bipolar Disorders, Schizophrenia and Schizophrenia-type Disorders, Major Depression or Posttraumatic Stress Disorders (PTSD). Females who are pregnant or lactating will also be excluded. We hypothesize that mecamylamine will result in a greater reduction of alcohol consumption than placebo among the alcohol dependent patients. We further hypothesize that mecamylamine will be effective in reducing both alcohol consumption and smoking in a subgroup of alcoholics who also smoke.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcoholism
Keywords
mecamylamine, treatment, alcohol dependence, smoking

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
136 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mecamylamine- Smoker
Arm Type
Experimental
Arm Title
Placebo-Smoker
Arm Type
Placebo Comparator
Arm Title
Mecamylamine- Non-Smoker
Arm Type
Experimental
Arm Title
Placebo-Non-Smoker
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
mecamylamine
Intervention Description
mecamylamine 10mg/day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Percent Heavy Drinking Days During Active Treatment Phase
Description
Data were calculated as number of heavy drinking days (heavy drinking days is defined as 5 drinks on a single occasion for men and 4 for women) average during 90 days of treatment.
Time Frame
12 weeks
Title
Self-report Weekly Craving Via Obsessive Compulsive Drinking Scale (OCDS)
Description
The OCDS is a 14-item (rated 0-4), self-administered questionnaire for characterizing and quantifying the obsessive and compulsive cognitive aspects of craving and heavy (alcoholic) drinking, such as drinking-related thought, urges to drink, and the ability to resist those thoughts and urges. A higher total score indicates higher craving and ranges from 0-48.
Time Frame
12 weeks
Title
Self-report Weekly Smoking Craving
Description
Questionnaire of smoking urges (QSU). It has 32 questions that range from 1 to 7, there are 8 questions per sub-scale. The total range is 32 to 224. Each sub-scale ranges from 8- 56, with a higher score indicating higher craving.
Time Frame
12 weeks
Title
Self-report Average Number of Cigarettes Per Day
Description
self-report from only the smoking population for cigarettes per day
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: individuals with DSM-IV diagnosis of alcohol dependence smokers and non-smokers patients who do not require psychotropic medication for the management of their psychiatric symptoms individuals with a history of substance dependence (other than alcohol and tobacco) but have not met criteria for substance dependence in the past 30 days women with acceptable method of contraception Exclusion Criteria: pregnant women medications thought to influence drinking behavior including: acamprosate, disulfiram, naltrexone and ondansetron underlying medical conditions history of glaucoma, prostatic hypertrophy, urethral obstruction, cerebral arteriosclerosis, pyloric stenosis, or a history of hypersensitivity to mecamylamine DSM-IV diagnosis of bipolar disorder, schizophrenia, and schizophrenia-type disorders unstable medical conditions patients who require psychotropic medication for the management of an active psychiatric disorder patients on pharmacological treatment for alcohol and/or nicotine dependence
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ismene Petrakis, M.D.
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Connecticut Healthcare System
City
West Haven
State/Province
Connecticut
ZIP/Postal Code
06516
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
29461925
Citation
Gandelman E, Petrakis I, Kachadourian L, Ralevski E. Negative Affect Intensity and Hostility in Individuals With Alcohol Use Disorder With or Without Posttraumatic Stress Disorder. J Dual Diagn. 2018 Apr-Jun;14(2):96-101. doi: 10.1080/15504263.2018.1434264. Epub 2018 Apr 25.
Results Reference
derived

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Treatment With Mecamylamine in Smoking and Non-smoking Alcohol Dependent Patients

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