Treatment With Mecamylamine in Smoking and Non-smoking Alcohol Dependent Patients
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.
|Study Design:||Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
|Official Title:||Treatment With Mecamylamine in Smoking and Non-smoking Alcohol Dependent Patients|
- self-report weekly alcohol consumption and smoking [ Time Frame: 12 weeks ] [ Designated as safety issue: Yes ]
- self-report weekly craving [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- self-report weekly smoking craving [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- side effects [ Time Frame: 12 weeks ] [ Designated as safety issue: Yes ]
|Study Start Date:||May 2004|
|Estimated Study Completion Date:||October 2014|
|Estimated Primary Completion Date:||October 2014 (Final data collection date for primary outcome measure)|
|Placebo Comparator: Mecamylamine||
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.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00342563
|Contact: Elizabeth Ralevski, Ph.D.||203-932-5711 ext firstname.lastname@example.org|
|Contact: Ismene Petrakis, M.D.||203-932-5711 ext email@example.com|
|United States, Connecticut|
|VA Connecticut Healthcare System||Recruiting|
|West Haven, Connecticut, United States, 06516|
|Contact: Ismene Petrakis, M.D. 203-932-5711 ext 2244 firstname.lastname@example.org|
|Contact: Elizabeth Ralevski, Ph.D. 203-932-5711 ext 4282 email@example.com|
|Principal Investigator: Ismene Petrakis, M.D.|
|Principal Investigator:||Ismene Petrakis, M.D.||Yale University|