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Clinical trial condition

Hyperoxaluria, Primary

Explore clinical trials studying Hyperoxaluria, Primary. Study availability and eligibility vary by location and protocol.

33 public trials 6 recruiting studies
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Hyperoxaluria, Primary trial results

Recruiting

Rare Kidney Stone Consortium Patient Registry

NCT00588562

Conditions
APRT Deficiency, Adenine phosphoribosyltransferase deficiency, Carbohydrate Metabolism, Inborn Errors, +19 more
Locations
  • 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
View Trial Details
Recruiting

Monogenic Kidney Stone - Genetic Testing

NCT03305835

Conditions
Adenine phosphoribosyltransferase deficiency, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +18 more
Locations
  • Mayo Clinic Rochester, Minnesota, United States
View Trial Details
Recruiting

Phase 1/2 Study of ABO-101 in Primary Hyperoxaluria Type 1 (redePHine)

NCT06839235

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +13 more
Locations
  • Mayo Clinic Rochester, Minnesota, United States
  • Nucleus Network Saint Paul, Minnesota, United States
  • Hospices Civils de Lyon- Hôpital Femmes Mères Enfants Lyon, France
  • Kindernierenzentrum Bonn Bonn, Germany
View Trial Details
Recruiting

Prospective Research Rare Kidney Stones (ProRKS)

NCT02780297

Conditions
Abnormalities, Multiple, Adenine Phosphoribosyltransferase Deficiency, Adenine phosphoribosyltransferase deficiency, +28 more
Locations
  • 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
View Trial Details
Completed

Nedosiran in Pediatric Patients From Birth to 11 Years of Age With PH and Relatively Intact Renal Function

NCT05001269

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +17 more
Locations
  • Clinical Research Site Rochester, Minnesota, United States
  • Clinical Research Site Hamilton, Ontario, Canada
  • Clinical Trial Site Bonn, Germany
  • Clinical Research Site Heidelberg, Germany
View all 13 locations
View Trial Details
Completed

Baby Detect : Genomic Newborn Screening

NCT05687474

Conditions
3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
Locations
  • CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
View Trial Details

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