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

Status: Recruiting
Location: See location...
Intervention Type: Other, Procedure
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Females and Males ≥ 18 years of age.

• Understands the procedures and agrees to participate by giving written informed consent.

⁃ Biopsy Group Only:

⁃ • Scheduled for standard of care liver biopsy for any reason.

⁃ Non-Biopsy Group Only:

⁃ • BMI ≥ 25, with or without type 2 diabetes, without any level of NAFLD based on: (1) Recent medical history (within 6 months of screening visit). (2) Data collected from participation in a prior research study where they consented to be re-contacted for future studies.

Locations
United States
Florida
AdventHealth Translational Research Institute
RECRUITING
Orlando
Contact Information
Primary
Recruitment Department
Fh.tri.recruitment@adventhealth.com
407-303-7100
Time Frame
Start Date: 2021-04-22
Estimated Completion Date: 2026-03
Participants
Target number of participants: 1250
Treatments
Biopsy Group
Adults undergoing a standard of care liver biopsy at AdventHealth Central Florida Division for any reason
Non-Biopsy Group
Adults without any history of NAFLD
Related Therapeutic Areas
Sponsors
Leads: AdventHealth Translational Research Institute
Collaborators: BPGbio

This content was sourced from clinicaltrials.gov