Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04807868

AdventHealth Research Institute Non-Alcoholic Fatty Liver Disease Biobank and Registry (AVAIL)

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,250 (estimated)
Sponsor
AdventHealth Translational Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to create a resource that will advance research that is focused on discovery of novel therapies, risk stratification, and aggressive interventions for those at highest risk for non-alcoholic fatty liver disease (NAFLD). To achieve this, we will generate a biobank of liver tissue collected during standard of care liver biopsies. Paired blood/urine samples, FibroScan and relevant data will also be collected.

Conditions

Interventions

TypeNameDescription
PROCEDUREStandard of care liver biopsyPatients undergoing a standard of care liver biopsy for any reason who are willing to participate will be consented for collecting additional biopsy tissue for research purposes. 1-2 additional biopsy tissue cores will be collected for research. Liver tissue will be biobanked for future use.
OTHERFibroscanA FibroScan will be performed to evaluate longitudinal changes in liver fat and fibrosis.
OTHERBiospecimen CollectionBlood and urine will be collected.

Timeline

Start date
2021-04-22
Primary completion
2025-12-01
Completion
2026-03-01
First posted
2021-03-19
Last updated
2025-03-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04807868. Inclusion in this directory is not an endorsement.