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Completed No phase listed Observational Accepts healthy volunteers Results available

Alcoholic Hepatitis Network Observational Study

ClinicalTrials.gov ID: NCT03850899

Public ClinicalTrials.gov record NCT03850899. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 20, 2026, 11:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this research study is to create a clinical database and bio-repository. To do this, we will obtain blood, urine, saliva, and stool samples (e.g., biological samples) and personal health information from you to use in future research studies related to alcoholic hepatitis or other diseases. Part of your blood sample will be used to extract your DNA. DNA is the genetic material that gives us unique characteristics. We are doing this research study because we are trying to find out more about how and why illnesses related to alcoholic hepatitis or other diseases occur in people. To do this, we will study the biological samples and personal health information from healthy and sick people. A "biological sample" is usually blood, but can be any body fluid. "Personal Health Information" includes such items as your name, age, gender, race, and/or your medical information. It can also include data from measurements and tests that you had while participating in another research study or that were done during the course of your regular medical care or doctor visits.

Study identification

NCT ID
NCT03850899
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Indiana University
Other
Enrollment
1,133 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 16, 2019
Primary completion
Jun 20, 2024
Completion
Jun 20, 2024
Last update posted
Feb 13, 2025

2019 – 2024

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
IU School of Medicine Indianapolis Indiana 46202-2879
University of Louisville Louisville Kentucky 40292
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
University Of Massachusetts Worcester Massachusetts 01655
Mayo Clinic Rochester Minnesota 55901
Cleveland Clinic Cleveland Ohio 44195
University of Pittsburgh Pittsburgh Pennsylvania 15260
University of Texas Southwestern Medical School Dallas Texas 75390
Virginia Commonwealth University Richmond Virginia 23284

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03850899, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 13, 2025 · Synced Sep 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03850899 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →