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Collects blood and liver samples to study liver diseases

Stores blood and liver samples for future research on liver disease.

Key facts

Who runs it
State University of New York at Buffalo
Where
Buffalo, United StatesSee the site
Trial code
Registry title
Blood Collection Biorepository for Liver Disease Research
Status
Recruiting
People taking part
1,000 people, planned
Started
Jul 2013
Expected to end
Dec 2099
Type of study
Observational
Record updated
8 October 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is collecting blood samples from people with or without liver disease. The samples will be stored for future liver research.

Age
7 Years and older
Sex
All sexes can join.
Disease stage
People with liver diseases such as viral hepatitis, liver cancer or NASH can join. People without liver disease can also join as comparison samples.

Main reasons for not taking part

  • Adults who cannot give consent
  • Infants
  • Pregnant women
  • Prisoners

The registry criteria, word for word

Show all 3 criteriaShow less

Who can take part

  • This protocol is to establish a biobank of blood samples from individuals with or without liver diseases including viral hepatitis, liver cancer, NASH, and negative control samples
  • Children and teenagers will be special populations considered in this protocol

Who cannot take part

  • Vulnerable populations such as adults unable to consent, infants, pregnant women or prisoners will not be considered for this research study

Where in United States

  • University at Buffalo, Buffalo General Medical CenterBuffalo, United StatesContact: Barbara Bauer, BATaking people

About the trial

What the trial wants to find out

The purpose of establishing a biorepository is to provide high quality specimens (serum, plasma, buffy coat and liver tissue) for future researchers who are studying the effects that fatty liver and viral diseases have on the liver.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Virology, Immunology and Mechanisms of Liver Disease in Patients With Hepatitis C and Other Liver Diseases
Plain-language title
Collects blood and liver samples to study liver diseasesGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
8 October 2026