NCT03489993
- Conditions
- Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +35 more
- Locations
-
- Wake Forest University Health Sciences Winston-Salem, North Carolina, United States
Clinical trial condition
Renal Tubular Transport, Inborn Errors
Explore clinical trials studying Renal Tubular Transport, Inborn Errors. Study availability and eligibility vary by location and protocol.
92 public trials
15 recruiting studies
Renal Tubular Transport, Inborn Errors trial results
NCT03920072
- Conditions
- Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +26 more
- Locations
-
- CHU de Bicetre Le Kremlin-Bicêtre, France
- Hopital Lariboisiere Paris, France
- Hopital Cochin Paris, France
- St. Vincent's University Hospital Dublin, Ireland
Completed
Effect of Urine Alkalinazation on Urinary Inflammatory Markers in Patients With Cystinuria
NCT03836144
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinuria, Female Urogenital Diseases, +18 more
- Locations
-
- Eurpean Georges Pompidou Hospital Paris, Île-de-France Region, France
NCT03663855
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinuria, Female Urogenital Diseases, +8 more
- Locations
-
- New York University School of Medicine New York, United States
NCT02125721
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinuria, Female Urogenital Diseases, +8 more
- Locations
-
- NYU Langone Medical Center New York, United States
NCT00195936
- Conditions
- Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +26 more
- Locations
-
- Section of Pediatric Nephrology, Children's Mercy Hospitals and Clinics Kansas City, Missouri, United States
Completed
X-linked Hypophosphatemia and FGF21
NCT03596554
- Conditions
- Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +26 more
- Locations
-
- Centre de Référence des Maladies Rénales Rares - Centre de Référence des Maladies Rares du Calcium et du Phosphate - Service de Néphrologie, Rhumatologie et Dermatologie Pédiatriques - Hôpital Femme Mère Enfant Bron, France
- Centre de Référence des Maladies Rares du Calcium et du Phosphore, Service d'Endocrinologie Pédiatrique - Hôpital du Kremlin Bicêtre Paris, France
- Endocrinologie, Maladies Osseuses, Gynécologie, Génétique, Hôpital des Enfants, CHU de Toulouse Toulouse, France
NCT02538016
- Conditions
- Calculi, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinuria, +15 more
- Locations
-
- Boston Children's Hospital Boston, Massachusetts, United States
Completed
Dent Disease Mutation Genotyping
NCT01783795
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dent Disease, Female Urogenital Diseases, +8 more
- Locations
-
- 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