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NCT07060547Recruiting

Investigating HepQuant DuO Test as a Biomarker in Alcohol-related Liver Disease

HepQuant, LLC

Start Date

6/10/2025

Completion Date

3/1/2032

Summary

This is a study to measure liver recovery in patients with recent alcohol-associated liver injury by assessing liver function and physiology using HepQuant DuO. The HepQuant DuO Test is a blood-based test that involves a drink of a natural compound, cholate, and 2 blood samples at 20 and 60 minutes. The study team is collecting clinical and laboratory data to better monitor and treat patients who have been affected by alcohol-associated liver disease. The study has 4 visits at an outpatient clinic at 1, 3, 6, and 12 months. At each of these visits, participants will undergo a HepQuant DuO test and other standard tests. In addition, the study team will ask about a participant's alcohol use, symptoms, and quality of life.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * adult with a clinical diagnosis of liver disease due to alcohol who have acute hepatic decompensation. adult with a combined clinical diagnosis of alcohol-related liver disease (ALD) and nonalcoholic steatohepatitis (NASH). Exclusion Criteria: * Clinical diagnosis of liver disease with an etiology other than alcohol liver disease unless it is a combined clinical diagnosis of ALD and NASH. * patients with solid organ malignancy. * patients with other disease affecting the liver including autoimmune, drug-related liver injury, hemochromatosis or Wilson's disease * pregnancy * under the age of 18

Interventions

DEVICE

HepQuant DuO Test

Interested in This Trial?

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Conditions

Alcoholic HepatitisAlcohol-related Liver Disease

Locations

Stanford University Dept. of Medicine -Gastroenterology & Hepatology

Redwood City, California 94063

United States