NCT02766855
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Cystine Crystals, Cystinosis, +6 more
- Locations
-
Not specified
Clinical trial condition
Cystinosis
Explore clinical trials studying Cystinosis. Study availability and eligibility vary by location and protocol.
41 public trials
9 recruiting studies
Cystinosis trial results
Completed
The Functional Consequences of the CTNS-deletion for the TRPV1-receptor in Cystinosis Patients
NCT02533076
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
- Locations
-
- Centre for Clinical Pharmacology, UZ Leuven Leuven, Vlaams-Brabant, Belgium
NCT00010426
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Disease Attributes, +9 more
- Locations
-
Not specified
NCT00001213
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT01432561
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +5 more
- Locations
-
- University of California, San Diego Center for Clinical Research Services (CCR) La Jolla, California, United States
NCT01614431
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Female Urogenital Diseases, +11 more
- Locations
-
Not specified
NCT00001736
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
- Locations
-
- National Eye Institute (NEI) Bethesda, Maryland, United States
NCT00004350
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Disease Attributes, +16 more
- Locations
-
Not specified
Completed
Establishment of a Database for Long-Term Monitoring of Patients With Nephropathic Cystinosis
NCT00004312
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Disease Attributes, +9 more
- Locations
-
- University of California San Diego School of Medicine La Jolla, California, United States
Active, Not Recruiting
Early Check: Expanded Screening in Newborns
NCT03655223
- Conditions
- 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
- Locations
-
- RTI International Research Triangle Park, North Carolina, United States