NCT07573059
- Conditions
- ARG1 Deficiency, Amino Acid Metabolism, Inborn Errors, Brain Diseases, +11 more
- Locations
-
- Rare Disease Research Atlanta, Georgia, United States
Clinical trial condition
Hyperargininemia
Explore clinical trials studying Hyperargininemia. Study availability and eligibility vary by location and protocol.
13 public trials
4 recruiting studies
Hyperargininemia trial results
NCT04908319
- Conditions
- ARGI Deficiency, ASL Deficiency, ASS Deficiency, +27 more
- Locations
-
- Children's National Medical Center Washington D.C., District of Columbia, United States
- Baylor College of Medicine Houston, Texas, United States
Recruiting
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
NCT01793168
- Conditions
- 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
- Locations
-
- Sanford Health Sioux Falls, South Dakota, United States
- Online Patient Enrollment System Sydney, Australia
NCT04602325
- Conditions
- Amino Acid Metabolism, Inborn Errors, Argininosuccinic Aciduria, Brain Diseases, +38 more
- Locations
-
- Children's National Research Institute Washington D.C., District of Columbia, United States
NCT06582524
- Conditions
- Amino Acid Metabolism, Inborn Errors, Arginase 1 Deficiency, Brain Diseases, +11 more
- Locations
-
- Univ. Klinik für Kinder- und Jugendheilkunde Medizinische Universität Graz, Austria
- Unidade de Doenças Metabólicas Pediatria, Hospital Santa Maria Lisbon, Portugal
- Bradford Royal Infirmary Duckworth Lane Bradford, United Kingdom
Completed
Improving Quality of Life and Daily Life Activities With Bioarginine in Patients With COPD
NCT05412160
- Conditions
- Amino Acid Metabolism, Inborn Errors, Argininemia, Brain Diseases, +24 more
- Locations
-
- L. Sacco Hospital Milan, Italy
Completed
Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
-
- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
NCT06683820
- Conditions
- Adenocarcinoma, Amino Acid Metabolism, Inborn Errors, Brain Diseases, +25 more
- Locations
-
- 2ndAffiliated Hospital, School of Medicine, Zhejiang University Hangzhou, Zhejiang, China
NCT03921541
- Conditions
- Amino Acid Metabolism, Inborn Errors, Arginase I Deficiency, Brain Diseases, +11 more
- Locations
-
- Harvey Pediatrics Rogers, Arkansas, United States
- Children's Hospital of Orange County Orange, California, United States
- Stanford University School of Medicine Stanford, California, United States
- Children's National Medical Center Washington D.C., District of Columbia, United States
NCT03378531
- Conditions
- Amino Acid Metabolism, Inborn Errors, Arginase I Deficiency, Brain Diseases, +11 more
- Locations
-
- Stanford University School of Medicine Stanford, California, United States
- University of Florida Gainesville, Florida, United States
- Icahn School of Medicine at Mount Sinai New York, United States
- UTSW Dallas, Texas, United States