Rare Kidney Stone Consortium Patient Registry | ClinicalTrials HQ

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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

4 results · Page 1 of 1

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Organizations	Linked trials
Mayo Clinic	970
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)	617
National Institutes of Health (NIH)	667
Oxalosis and Hyperoxaluria Foundation (OHF)	1

4 results · Page 1 of 1

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Research sites	City	Country	Linked trials
APRT Registry - Landspitali Universtiy Hospital	Reykjavik	Iceland	1
Cystinuria Registry - New York University	New York	United States	1
Dent Disease Registry -Mayo Clinic	Rochester	United States	1
Primary Hyperoxaluria Registry - Mayo Clinic	Rochester	United States	1