Expired Study
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New York, New York 10029


Purpose:

This study is a double-blind, placebo-controlled outpatient trial to improve, through the addition of sertraline (Zoloft), the abstinence and relapse rates in alcohol- dependent individuals currently taking naltrexone (Revia).


Criteria:

Inclusion Criteria: - Meets the criteria for alcohol dependence. - Abstinent from alcohol for a period of at least 5 days and not greater than 30 days. - Able to read English and complete study evaluations. - A stable residence and a telephone to ensure that subjects can be located during the study. Exclusion Criteria: - Currently meets criteria for substance abuse or dependence with the exception of nicotine dependence. - Current use of disulfiram (Antabuse) or a MAO Inhibitor. - Psychotic or otherwise severely psychiatrically disabled (i.e., depressed, suicidal, current mania). - Major depression at the time of assessment. - Previous treatment with naltrexone (Revia) for alcohol dependence. - Significant underlying medical conditions such as cerebral, renal, thyroid, or cardiac disease. - Abstinent longer than 30 days prior to admission to program. - Hepatocellular disease or elevated bilirubin levels. - Females who are pregnant, nursing, or not using a reliable method of birth control.


NCT ID:

NCT00000440


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

New York, New York 10029
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: July 22, 2017

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