Actively Recruiting
Investigating HepQuant DuO Test as a Biomarker in Alcohol-related Liver Disease
Led by HepQuant, LLC · Updated on 2025-07-11
40
Participants Needed
1
Research Sites
350 weeks
Total Duration
On this page
Sponsors
H
HepQuant, LLC
Lead Sponsor
L
Leland Stanford Junior University
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Investigating HepQuant DuO Test as a Biomarker in Alcohol-related Liver Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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)
You will not qualify if you...
- Clinical diagnosis of liver disease with an etiology other than alcohol liver disease unless combined ALD and NASH
- Patients with solid organ malignancy
- Patients with other liver disease including autoimmune, drug-related injury, hemochromatosis, or Wilson's disease
- Pregnancy
- Under the age of 18
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Stanford University Dept. of Medicine -Gastroenterology & Hepatology
Redwood City, California, United States, 94063
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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