CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 111 enrolled
Drug / intervention
memantine +2 moredrug
Likely dose
memantine 20 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00630955
NCT00630955Phase 2Completed

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

Yale University·interventional·Posted Mar 7, 2008·Updated Mar 17, 2020

In Brief

A Phase 2 clinical trial evaluating memantine, Memantine, and 1 other intervention for Alcohol Drinking. Completed, enrolled 111 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 7, 2008
Enrollment StartJun 1, 2006
Primary CompletionMay 1, 2011
Study CompletionAug 1, 2011
TodayJul 2, 2026
Enrollment to primary: 4.9 yearsPosted 18.3 years ago

Interventions

memantinedrug

Memantine 20 mg once per day for 7 days

Memantinedrug

Memantine 40 mg once per day for 7 days

Placebodrug

Placebo once per day for 7 days