Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Paris, France6 results · Page 1 of 1
Clinical trials
Swipe the table sideways for more columns.
| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Follow-up Gene Therapy Trial for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR Gene | X-Linked Retinitis Pigmentosa | Active, not recruiting | Phase 3 | 2026-09-25 | NCT04794101 | |
| Rate of Progression in USH2A-related Retinal Degeneration | Usher syndrome type 2A, retinitis pigmentosa 39 | Active, not recruiting | Not stated | 2026-07-23 | NCT03146078 | |
| High Resolution, High-speed Multimodal Ophthalmic Imaging | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, age-related macular degeneration, brain disorder, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, corneal disorder, corneal dystrophy, diabetes mellitus, dry eye syndrome, endocrine system disorder, eye disorder, glaucoma, glucose metabolism disease, hereditary disease, hypertensive disorder, inherited retinal dystrophy, injury, keratoconus, lacrimal apparatus disorder, macular degeneration, macular retinal edema, metabolic disease, nervous system disorder, ocular hypertension, retinal degeneration, retinal detachment, retinal disorder, retinitis pigmentosa, stroke disorder, vascular disorder | Recruiting | Not applicable | 2025-11-18 | NCT04129021 | |
| Feasibility and Tolerability Study of Smart Contact Lens With Healthy Subjects and Patients With Stargardt's Disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorder | Not yet recruiting | Not applicable | 2025-09-18 | NCT06989658 | |
| oCular Examination at Cell RESolution With Optical TransmissionTomography | Glaucoma Associated With Other Ocular Disorders | Recruiting | Not applicable | 2025-05-16 | NCT06976034 | |
| Natural History Study of Usher Syndrome ( Light4Deaf ) | Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Usher syndrome, blindness (disorder), eye disorder, hearing disorder, hearing loss disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorder | Recruiting | Not stated | 2020-12-14 | NCT04665726 |