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Liver Disease in Urea Cycle Disorders
Sponsor: Baylor College of Medicine
Summary
This is a multi-center, cross-sectional study to assess risk for liver fibrosis and hepatic injury in individuals with urea cycle disorders (UCDs) using serum biomarkers, Fibroscan, and MRE. This study will be conducted at 5 sites of the Urea Cycle Disorders Consortium: Baylor College of Medicine in Houston, TX, Seattle Children's Hospital in Seattle, WA, Children's Hospital Colorado in Aurora, CO, Children's Hospital of Philadelphia in Philadelphia, PA, and Children's National Medical Center in Washington D.C.
Official title: Noninvasive Biomarkers of Hepatic Fibrosis in Urea Cycle Disorders
Key Details
Gender
All
Age Range
6 Years - 65 Years
Study Type
OBSERVATIONAL
Enrollment
62
Start Date
2021-11-04
Completion Date
2025-12-31
Last Updated
2025-04-17
Healthy Volunteers
No
Conditions
Locations (5)
Children's Hospital Colorado
Aurora, Colorado, United States
Children's National Medical Center
Washington D.C., District of Columbia, United States
The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Baylor College of Medicine
Houston, Texas, United States
Seattle Children's Hospital
Seattle, Washington, United States