NCT04912843
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +13 more
- Locations
-
- Beijing Tongren Hospital, Capital Medical University Beijing, China
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
Not yet recruiting
Mechanisms of Fecal Incontinence in Wolfram Syndrome
NCT07313085
- Conditions
- Abnormalities, Multiple, Blindness, Congenital Abnormalities, +40 more
- Locations
-
- HEGP Paris, France
Not yet recruiting
Pilot Study of the Efficacy of Nicotinamide (Vitamin B3) in Leber's Hereditary Optic Neuropathy
NCT07258667
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +16 more
- Locations
-
- Angers University Hospital Angers, France
Not yet recruiting
Optic Nerve Head Evaluation Through Multimodal Blood Flow Analysis: a Prospective Observational, Multi-center Study
NCT07075887
- Conditions
- Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, +24 more
- Locations
-
Not specified
Active, not recruiting
AMX0035 in Adult Patients With Wolfram Syndrome
NCT05676034
- Conditions
- Abnormalities, Multiple, Blindness, Congenital Abnormalities, +35 more
- Locations
-
- Washington University St Louis, Missouri, United States
Active, not recruiting
A Phase 3, Multicenter, Randomized, Double-Masked, Sham-Controlled Clinical Trial for Leber's Hereditary Optic Neuropathy (LHON) Associated With ND4 Mutation
NCT07406854
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +13 more
- Locations
-
- Beijing Tongren Hospital, Capital Medical University Beijing, Beijing Municipality, China
Active, not recruiting
Gene Therapy Clinical Trial for the Treatment of Leber's Hereditary Optic Neuropathy Associated With ND4 Mutations
NCT05293626
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +13 more
- Locations
-
- Stanford Byers Eye Institute Palo Alto, California, United States
- University of Colorado Health Eye Center Aurora, Colorado, United States
- Wills Eye Hospital, Neuro Ophthalmology Department Philadelphia, Pennsylvania, United States
Active, not recruiting
A Study to Evaluate Efficacy, Safety, Tolerability and Exposure After a Repeat-dose of Sepofarsen (QR-110) in LCA10 (ILLUMINATE)
NCT03913143
- Conditions
- Blindness, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +26 more
- Locations
-
- University of Iowa Iowa City, Iowa, United States
- Universitair Ziekenhuis Gent (UZ) Ghent, Belgium
- INRET Clínica/ Santa Casa de Misericórdia de Belo Horizonte Belo Horizonte, Minas Gerais, Brazil
- Federal University of São Paulo - Hospital São Paulo (UNIFESP-HSP) São Paulo, Brazil
NCT03951298
- Conditions
- Abnormalities, Multiple, Blindness, Congenital Abnormalities, +37 more
- Locations
-
- Washington University School of Medicine St Louis, Missouri, United States
NCT03717909
- Conditions
- Abnormalities, Multiple, Blindness, Congenital Abnormalities, +35 more
- Locations
-
- CHU de Montpellier, Hopital Gui de Chauliac Montpellier, France
- Hôpital Européen Georges-Pompidou Paris, France
- Medical University of Lodz Lodz, Poland
- Unidad de Gestión Clínica Almería Periferia. Distrito Sanitario Almería Almería, Spain