Rare Kidney Stone Consortium Biobank
Rare Kidney Stone Consortium Biobank
Recruiting · NCT02026388 · Registry updated 2026-07-22Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Rare Kidney Stone Consortium Biobank | 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, primary hyperoxaluria type 1, primary hyperoxaluria type 2, renal aminoaciduria, renal tubular transport disease, urinary system disorder | Recruiting | Not stated | 2026-07-22 | NCT02026388 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Mayo Clinic | 970 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Mayo Clinic | Rochester | United States | 664 |