Clinical Trial

Endotoxin Exposure to Examine the Role of Inflammation in Alcohol Use

Not Yet Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
The study design consists of a randomized, double-blind, placebo-controlled study of low dose endotoxin. Individuals with current AUD (n=32) and matched controls without AUD (n=32) will be randomly assigned to receive a single intravenous (I.V.) infusion of either low dose endotoxin (0.8 ng/kg of body weight) or placebo (same volume of 0.9% saline solution) to determine the acute and protracted role of inflammation in alcohol use.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2026-02-27; most recent amendment 2026-04-28.
Trial Details
NCT Number NCT07452146
Lead Sponsor University of California, Los Angeles
Collaborators: National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Conditions Alcohol Use Disorder, Inflammatory Response, Craving
Enrollment 64 participants
Start Date 2026-06
Primary Completion 2028-06 (estimated)
Study Completion 2028-07 (estimated)
Updated on ClinicalTrials.gov 2026-05-04