NCT02202694
- Conditions
- Color Vision Defects, Cone Dystrophy, Eye Diseases, +11 more
- Locations
-
- Dow University of Health Sciences Karachi, Sindh, Pakistan
Clinical trial condition
Eye Diseases, Hereditary
Explore clinical trials studying Eye Diseases, Hereditary. Study availability and eligibility vary by location and protocol.
849 public trials
191 recruiting studies
Eye Diseases, Hereditary trial results
Completed
Molecular Analysis of Retinoblastoma
NCT00718783
- Conditions
- Eye Diseases, Eye Diseases, Hereditary, Eye Neoplasms, +11 more
- Locations
-
- Hospital Calvo Mackenna Santiago, Santiago Metropolitan, Chile
- Hospital Escuela Bloque Materno Infantil Tegucigalpa, Honduras
NCT00857519
- Conditions
- Eye Diseases, Eye Diseases, Hereditary, Eye Neoplasms, +11 more
- Locations
-
- Oncology Service, Wills Eye Institute Philadelphia, Pennsylvania, United States
Completed
Genetic Decryption of Leber Congenital Amaurosis (LCA) in a Large Cohort of Independent Families.
NCT02970266
- Conditions
- Eye Diseases, Eye Diseases, Hereditary, Leber Congenital Amaurosis, +1 more
- Locations
-
- Necker-Enfants Malades Hospital Paris, France
Completed
CNTF Implants for CNGB3 Achromatopsia
NCT01648452
- Conditions
- Achromatopsia, Color Vision Defects, Cone Dystrophy, +9 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT01603576
- Conditions
- Choroid Diseases, Choroideremia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
- Locations
-
- Nicta / Data61 Canberra, Australian Capital Territory, Australia
- Centre for Eye Research Australia East Melbourne, Victoria, Australia
NCT00336076
- Conditions
- Albinism, Amino Acid Metabolism, Inborn Errors, Anaphylaxis, +21 more
- Locations
-
- University of Michigan Ann Arbor, Michigan, United States
NCT01610973
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Diseases, Corneal Dystrophies, Hereditary, +5 more
- Locations
-
- UH Rouen Rouen, France
NCT02875145
- Conditions
- Cataract, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Diseases, +7 more
- Locations
-
- Ophthalmology Department, CHU Besançon Besançon, France
NCT01979250
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Diseases, Corneal Dystrophies, Hereditary, +5 more
- Locations
-
- Department of Ophthalmology Aarhus, Aarhus C, Denmark