Actively Recruiting
Functional Neuroimaging of Alcoholism Vulnerability: Probing Glutamate and Reward, Using the mGluR5 Inhibitor Mavoglurant
Led by Yale University · Updated on 2025-10-09
80
Participants Needed
1
Research Sites
219 weeks
Total Duration
On this page
Sponsors
Y
Yale University
Lead Sponsor
N
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the role of Mavoglurant in clarifying the neurobiology of alcoholism risk. This is a one-site, randomized, within subjects, counterbalanced double-blind study of a single dose (200mg) of Mavoglurant and placebo.
CONDITIONS
Official Title
Functional Neuroimaging of Alcoholism Vulnerability: Probing Glutamate and Reward, Using the mGluR5 Inhibitor Mavoglurant
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ages 18-45 years
- Estimated full-scale IQ greater than 70
- Ability to cooperate with all study procedures
- No history of neurological disorders such as epilepsy
- No major medical conditions like cancer
- No history of significant head trauma
- Stable medication treatment for at least 6 weeks before enrollment
- Negative urine drug and breath alcohol tests at the time of MRI scan
- Negative urine pregnancy test at the time of MRI scan
- No MRI contraindications such as in-body metal implants or severe claustrophobia
- No contraindications to the study drug
You will not qualify if you...
- Any diagnosis of psychotic disorders or current mood or anxiety disorders
- Severe alcohol use disorder or current substance use disorder (mild or moderate alcohol use disorder allowed if no craving, tolerance, or withdrawal in past 3 months)
- Psychotic disorder reported in a first-degree relative
- Auditory or visual impairments that interfere with test-taking
- Prenatal alcohol exposure plus current features of fetal alcohol syndrome
- Not fluent in English or primarily educated in a non-English language beyond grade 1
- Intellectual disability with full-scale IQ below 70
- Traumatic brain injury with loss of consciousness over 30 minutes or concussion in past 30 days
- History of neurosurgery or neurologic illness affecting brain function including epilepsy or multiple sclerosis
- Major medical conditions such as cancer or heart failure
- Current pregnancy or not using effective birth control to prevent drug exposure to fetus
- Current substance use except marijuana if last use was more than 24 hours before visit
- Inability to understand consent or cooperate with study procedures
- MRI exclusions including metal devices, clips, or fragments in the body
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Trial Site Locations
Total: 1 location
1
Hartford Hospital
Hartford, Connecticut, United States, 06106
Actively Recruiting
Research Team
G
Godfrey D Pearlson, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
4
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