NCT03475173
- Conditions
- Acute Zonal Occult Outer Retinopathy, Acute zonal occult outer retinopathy, Arterial Occlusive Diseases, +31 more
- Locations
-
- University of Iowa Department of Ophthalmology Iowa City, Iowa, United States
Clinical trial condition
Optic Atrophies, Hereditary
Explore clinical trials studying Optic Atrophies, Hereditary. Study availability and eligibility vary by location and protocol.
43 public trials
11 recruiting studies
Optic Atrophies, Hereditary trial results
NCT07729982
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +13 more
- Locations
-
- Department of Ophthalmology, LMU University Hospital, LMU Medizin, Ludwig-Maximilians-Universität München Munich, Bavaria, Germany
Recruiting
Stem Cell Ophthalmology Treatment Study II
NCT03011541
- Conditions
- Abnormalities, Multiple, Age-Related Macular Degeneration, Autoimmune Diseases, +75 more
- Locations
-
- MD Stem Cells Westport, Connecticut, United States
- MD Stem Cells Coral Springs, Florida, United States
- MD Stem Cells Kobinia Med Vienna, Austria
- The Saudi-German Hospital Dubai, United Arab Emirates
Recruiting
Study to Evaluate Sepofarsen in Subjects With Leber Congenital Amaurosis (LCA) Type 10 (HYPERION)
NCT06891443
- Conditions
- Blindness, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +28 more
- Locations
-
- UCSF Wayne and Gladys Valley Center for Vision San Francisco, California, United States
- University of Miami - Bascom Palmer Eye Institute Miami, Florida, United States
- University of Iowa Iowa City, Iowa, United States
- University of Minnesota Medical School Minneapolis, Minnesota, United States
Recruiting
Efficacy and Safety Study of Bilateral IVT Injection of GS010 at Two Dose Levels in LHON Patients
NCT07303296
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +13 more
- Locations
-
- Hopital national des quinze-vingts Paris, France
Recruiting
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)
NCT01694940
- Conditions
- Abnormalities, Multiple, Acid-Base Imbalance, Acidosis, +86 more
- Locations
-
- University of California San Diego San Diego, California, United States
- Lucile Packard Children's Hospital Stanford, California, United States
- Children's Hospital of Colorado Aurora, Colorado, United States
- Children's National Medical Center Washington D.C., District of Columbia, United States
NCT02841553
- Conditions
- Abnormalities, Multiple, Ataxia, Blindness, +40 more
- Locations
-
- Washington University School of Medicine St Louis, Missouri, United States
NCT06682819
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +14 more
- Locations
-
- HEGP Paris, 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
Monogenic Diabetes Misdiagnosed as Type 1
NCT03988764
- Conditions
- Abnormalities, Multiple, Autoimmune Diseases, Blindness, +43 more
- Locations
-
- The Montreal Children's Hospital Montreal, Quebec, Canada