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RECRUITING
NCT04612764

Liver Disease in Urea Cycle Disorders

Sponsor: Baylor College of Medicine

View on ClinicalTrials.gov

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

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