NCT00359684
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
- Locations
-
- National Institutes of Health Clinical Center Bethesda, Maryland, United States
Clinical trial condition
Cystinosis
Explore clinical trials studying Cystinosis. Study availability and eligibility vary by location and protocol.
41 public trials
10 recruiting studies
Cystinosis trial results
Recruiting
Cystinosis and Mitochondrial Metabolism
NCT07319091
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +9 more
- Locations
-
- Service de néphrologie pédiatrique, Hôpital Femme Mère Enfant, Hospices Civils de Lyon Bron, France
- Service de Néphrologie pédiatrique, Hôpital Jeanne de Flandre Lille, France
- Service de néphrologie et exploration fonctionnelle rénale, Hôpital Edouard Herriot, Hospices Civils de Lyon Lyon, France
- Service de Néphrologie pédiatrique, Hôpital de la Timone Marseille, France
NCT06910813
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Fanconi Syndrome, +13 more
- Locations
-
- University of California at San Diego - Rady Children's Hospital San Diego, California, United States
- Stanford University - Stanford Children's Health Stanford, California, United States
- Emory University School of Medicine - Children's Healthcare of Atlanta (recuiting Cohort 0) Atlanta, Georgia, United States
- Baylor College of Medicine - Texas Children's Hospital (recuiting Cohort 0) Houston, Texas, United States
Recruiting
European Cystinosis Cohort
NCT05901077
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
- Locations
-
- RaDiCo-ECYSCO Paris, Île-de-France Region, France
Recruiting
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
NCT01793168
- Conditions
- 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
- Locations
-
- Sanford Health Sioux Falls, South Dakota, United States
- Online Patient Enrollment System Sydney, Australia
Recruiting
CYSTEA-BONE Clinical Study
NCT03919981
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +5 more
- Locations
-
- CHU de Besançon Besançon, France
- CHU Bordeaux - Hôpital Pellegrin tripode Bordeaux, France
- Hôpital Femme Mère Enfant Bron, France
- Hôpital Jeanne de Flandre Lille, France
NCT05959668
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
- Locations
-
- University Medical Center Hamburg-Eppendorf | Center for Psychosocial Medicine | Department of Medical Psychology Hamburg, Germany
NCT06213402
- Conditions
- Anemia, Anemia Due to Membrane Defect, Anemia, Hemolytic, +29 more
- Locations
-
- Vall d'hebron Research Institute - Vall d'Hebron Research Institute - University Hospital Vall d'Hebrón (VHIR/HUVH) Barcelona, Catalonia, Spain
Recruiting
National Registry of Rare Kidney Diseases
NCT06065852
- Conditions
- AH Amyloidosis, AHL Amyloidosis, AL Amyloidosis, +207 more
- Locations
-
- Zoe Plummer Bristol, South West, United Kingdom
NCT05508009
- Conditions
- Autoimmune Diseases, CKD Stage 4, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +22 more
- Locations
-
- Lucile Packard Children's Hospital Palo Alto, California, United States