RecruitingPhase 2NCT05781009

Pregnenolone for the Treatment of Alcohol Use Disorder


Sponsor

Yale University

Enrollment

150 participants

Start Date

Jan 8, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This Phase 2 randomized cotrolled trial (RCT) will assess the safety and efficacy of pregnenolone (PREG; 300 mg/day, b.i.d dosing) vs. placebo (PBO) over a 12 week treatment period, and at 1-month post-treatment follow-up in individuals with Alcohol Use Disorder (AUD).


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Placebo and a drug called Pregnenolone for people with alcohol use disorder. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 70 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPregnenolone

300mg

DRUGPlacebo

placebo


Locations(1)

The Yale Stress Center: Yale University

New Haven, Connecticut, United States

View Full Details on ClinicalTrials.gov

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NCT05781009


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