Clinical Trials Directory

Trials / Completed

CompletedNCT00630955

Family History Study of Alcohol Consumption Using Memantine

NMDA Antagonist Efficacy in Reducing Human Alcohol Consumption: Impact of Family History

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
111 (actual)
Sponsor
Yale University · Academic / Other
Sex
All
Age
21 Years – 50 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGmemantineMemantine 20 mg once per day for 7 days
DRUGMemantineMemantine 40 mg once per day for 7 days
DRUGPlaceboPlacebo once per day for 7 days

Timeline

Start date
2006-06-01
Primary completion
2011-05-01
Completion
2011-08-01
First posted
2008-03-07
Last updated
2020-03-17
Results posted
2014-03-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00630955. Inclusion in this directory is not an endorsement.