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Showing 1–11 of 11 trials
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Published and searchable clinical trials
Rare Kidney Stone Consortium Biobank
NCT02026388
- Conditions
- APRT Deficiency, Adenine phosphoribosyltransferase deficiency, Carbohydrate Metabolism, Inborn Errors, +21 more
- Locations
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- Mayo Clinic Rochester, Minnesota, United States
NCT00588562
- Conditions
- APRT Deficiency, Adenine phosphoribosyltransferase deficiency, Carbohydrate Metabolism, Inborn Errors, +19 more
- Locations
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- Dent Disease Registry -Mayo Clinic Rochester, Minnesota, United States
- Primary Hyperoxaluria Registry - Mayo Clinic Rochester, Minnesota, United States
- Cystinuria Registry - New York University New York, United States
- APRT Registry - Landspitali Universtiy Hospital Reykjavik, Iceland
Monogenic Kidney Stone - Genetic Testing
NCT03305835
- Conditions
- Adenine phosphoribosyltransferase deficiency, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +18 more
- Locations
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- Mayo Clinic Rochester, Minnesota, United States
Ultrasound for Socket Healing Evaluation
NCT06017193
- Conditions
- Alveolar Bone Loss, Alveolar; Wound, Bone Diseases, +20 more
- Locations
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- Ohio State University Columbus, Ohio, United States
NCT02780297
- Conditions
- Abnormalities, Multiple, Adenine Phosphoribosyltransferase Deficiency, Adenine phosphoribosyltransferase deficiency, +28 more
- Locations
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- University of Alabama @ Birmingham Birmingham, Alabama, United States
- Mayo Clinic Jacksonville Jacksonville, Florida, United States
- Children's Memorial Hospital Chicago, Illinois, United States
- Children's Hospital, Harvard Medical School Boston, Massachusetts, United States
National Registry of Rare Kidney Diseases
NCT06065852
- Conditions
- AH Amyloidosis, AHL Amyloidosis, AL Amyloidosis, +207 more
- Locations
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- Zoe Plummer Bristol, South West, United Kingdom
NCT04459013
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dent Disease, Female Urogenital Diseases, +8 more
- Locations
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- Service Odontology, Hôpital Pitié-Salpêtrière Paris, Île-de-France Region, France
NCT02124395
- Conditions
- Adenine Phosphoribosyl Transferase Deficiency, Adenine phosphoribosyltransferase deficiency, Carbohydrate Metabolism, Inborn Errors, +19 more
- Locations
-
- Primary Hyperoxaluria and Dent Disease Registry - Mayo Clinic Rochester, Minnesota, United States
- New York University School of Medicine - Cystinuria Registry New York, United States
- APRT Registry - Landspitali Universtiy Hospital Reykjavik, Iceland
Dent Disease Mutation Genotyping
NCT01783795
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dent Disease, Female Urogenital Diseases, +8 more
- Locations
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- Mayo Clinic Rochester, Minnesota, United States
NCT02016235
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dent Disease, Female Urogenital Diseases, +8 more
- Locations
-
- Mayo Clinic Rochester, Minnesota, United States
NCT02022189
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dent Disease, Female Urogenital Diseases, +8 more
- Locations
-
- Mayo Clinic Rochester, Minnesota, United States