Oxalosis and Hyperoxaluria Foundation (OHF)

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Rare Kidney Stone Consortium Patient Registry	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, cystinuria, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, kidney disorder, metabolic disease, primary hyperoxaluria, renal aminoaciduria, renal tubular transport disease, urinary system disorder	Recruiting	Not stated	2026-07-10		NCT00588562

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