maple syrup urine disease | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
MyRareDiet A Novel Diet Tracking Tool	Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, maple syrup urine disease, metabolic disease, methylmalonic acidemia, nervous system disorder, propionic acidemia, urea cycle disorder	Not yet recruiting	Not applicable	2024-10-30		NCT06664840
Systemic Biomarkers of Brain Injury From Hyperammonemia	Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypoxia, Hypoxia, Brain, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Signs and Symptoms, Respiratory, X-linked disease, arginase deficiency, argininosuccinic aciduria, brain disorder, brain hypoxia - ischemia, brain ischemia, carbamoyl phosphate synthetase I deficiency disease, cardiovascular disorder, carnitine-acylcarnitine translocase deficiency, central nervous system disorder, cerebrovascular disorder, citrullinemia, glutaryl-CoA dehydrogenase deficiency, hereditary disease, hyperammonemia due to N-acetylglutamate synthase deficiency, inborn disorder of amino acid metabolism, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inborn organic aciduria, maple syrup urine disease, medium chain acyl-CoA dehydrogenase deficiency, metabolic disease, mitochondrial trifunctional protein deficiency, nervous system disorder, ornithine carbamoyltransferase deficiency, ornithine translocase deficiency, perinatal asphyxia, urea cycle disorder, vascular disorder, very long chain acyl-CoA dehydrogenase deficiency	Recruiting	Not stated	2024-02-07		NCT04602325