Expired Study
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New Haven, Connecticut 06519


Purpose:

The purpose of this study is to evaluate the effects of the study medication, memantine (placebo, 20 mg or 40 mg/day) on alcohol drinking behavior in a laboratory setting in which participants are given an initial drink of alcohol followed by the choice to drink up to 12 more drinks over a three-hour period. We hypothesize that memantine will reduce craving and number of drinks consumed prior to and after exposure to the initial drink of alcohol and during the three hour drinking period. We will also evaluate the influence of family history of alcoholism on the efficacy of memantine in reducing alcohol drinking behavior.


Criteria:

Inclusion Criteria: - Ages 21-50 - Able to read English at 6th grade level or higher and to complete study evaluations - Regular alcohol drinker Exclusion Criteria: - Individuals who are seeking alcohol treatment - Medical conditions that would contraindicate the use of memantine - Regular use of other substances


NCT ID:

NCT00630955


Primary Contact:

Principal Investigator
Suchitra Krishnan-Sarin, Ph.D.
Yale School of Medicine


Backup Contact:

N/A


Location Contact:

New Haven, Connecticut 06519
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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