Ketamine/Placebo Family History Positive Study

Brief Summary

The proposed study is the first to explore the contribution of brain glutamate systems, a major target of ethanol in the brain, to the vulnerability to develop alcoholism. This study may lead to an enhanced understanding of the underlying neurobiological mechanism in high-risk individuals that may lead to the transition from moderate to excessive use of alcohol.

Intervention / Treatment

  • Drug: Ketamine and Placebo

Condition or Disease

  • Alcoholism

Phase

Study Design

Study type: Interventional
Status: Completed
Study results: Has Results
Age: 21 Years to 30 Years   (Adult)
Enrollment: 99 ()
Funded by: Other|U.S. Fed|NIH

Masking

Clinical Trial Dates

Start date: Mar 01, 2020
Primary Completion: Jun 15, 2020
Completion Date: Jun 15, 2020
Study First Posted: Jan 09, 2008
Results First Posted: Mar 03, 2017
Last Updated: Mar 03, 2017

Sponsors / Collaborators

Lead Sponsor: N/A
Responsible Party: N/A

Males and females with a paternal family history of alcoholism have a high risk for developing alcoholism. These individuals have been shown to decrease dysphoric responses to alcohol self-administration that may promote the excessive use of alcohol. Ethanol has been shown to be an antagonist at the N-methyl-D-aspartate (NMDA) glutamate receptor. We have recently shown that sober alcoholics have decreased dysphoric response to the NMDA antagonist, ketamine. We propose to test the hypothesis that this characteristic exists as a vulnerability factor in those individuals susceptible to develop alcoholism. Specifically, the objective is to determine whether individuals with a family history positive (FHP) for alcoholism will experience less dysphoric, anxiogenic, and psychotogenic effects to ketamine infusion when compared to family history negative (FHN) control subjects.

Male and female subjects, FHP (biological father and one other first degree relative) between the ages of 21-30, and matched controls (FHN) will complete 2 test days in a randomized balanced order under double-blind conditions. Test days will involve the 60-minute intravenous infusion of placebo and ketamine. Outcome measures include the Biphasic Alcohol Scale and visual analog scales for mood states. Secondary measures include visual analog scales for high, similarity to ethanol, the Sensation Scale (a validated measure of ethanol-like sensations) and aspects of craving for alcohol.

Eligibility Criteria

Sex: All
Minimum Age: 21
Maximum Age: 30

More Details

NCT Number: NCT00588952
Other IDs: 0103012310|VA Alcohol Research Center|P50AA012870
Study URL: https://ClinicalTrials.gov/show/NCT00588952
Last updated: Jan 28, 2021