Cincinnati Children's Hosptial Medical Center

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Prospective Research Rare Kidney Stones (ProRKS)	Abnormalities, Multiple, Amino Acid Transport Disorders, Inborn, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dent disease, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hyperoxaluria, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Diseases, X-linked disease, adenine phosphoribosyltransferase deficiency, brain disorder, central nervous system disorder, cystinuria, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, kidney disorder, metabolic disease, nervous system disorder, oculocerebrorenal syndrome, primary hyperoxaluria, renal aminoaciduria, renal tubular transport disease, urinary system disorder	Recruiting	Not stated	2026-08-07		NCT02780297

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