Hepatic Histopathology in Urea Cycle Disorders
Hepatic Histopathology in Urea Cycle Disorders
Recruiting · NCT04908319 · Registry updated 2025-07-20Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Hepatic Histopathology in Urea Cycle Disorders | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Citrullinemia 1, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, X-linked disease, arginase deficiency, argininosuccinic aciduria, brain disorder, carbamoyl phosphate synthetase I deficiency disease, central nervous system disorder, citrullinemia, hereditary disease, hyperammonemia due to N-acetylglutamate synthase deficiency, inborn disorder of amino acid metabolism, inborn errors of metabolism, inborn mitochondrial metabolism disorder, liver disorder, metabolic disease, nervous system disorder, ornithine carbamoyltransferase deficiency, urea cycle disorder | Recruiting | Not stated | 2025-07-20 | NCT04908319 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Baylor College of Medicine | 267 |
| Children's National Research Institute | 84 |
2 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Baylor College of Medicine | Houston | United States | 306 |
| Children's National Medical Center | Washington D.C. | United States | 177 |