Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Explore linked clinical trials.15 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| AOSLO Imaging for the Study of Cellular Alterations in Retinal Neurodegeneration | eye disorder, retinal disorder | Not yet recruiting | Not applicable | 2026-07-24 | NCT07725055 | |
| Implementation and Evaluation of a Post-Diagnostic Announcement Protocol at the CRMR RefeRet, Quinze-Vingts Hospital | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosa | Recruiting | Not applicable | 2026-02-10 | NCT07292987 | |
| Natural History of Photoreceptor Degeneration in USH1B: Clinical Parameters and Validation of Functional Vision Tests in MYO7A | 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 | 2026-02-10 | NCT07278843 | |
| 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 | |
| Describe the Progression of Inflammatory Orbitopathy and the Biological Progression of Patients Receiving Second-line Treatment | Graves disease, autoimmune disease, disease of orbital part of eye adnexa, endocrine system disorder, exophthalmos, eye disorder, goiter, hyperthyroidism, immune system disorder, thyroid gland disorder | Recruiting | Not stated | 2025-08-15 | NCT07117981 | |
| 100 High Myopia Patient-reported Outcomes (PRO) and Performance Outcomes (PERFO) | High Myopia | Not yet recruiting | Not applicable | 2025-08-03 | NCT07101146 | |
| Study of BEST1 Vitelliform Macular Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, retinal degeneration, retinal disorder, retinitis pigmentosa, vitelliform macular dystrophy | Recruiting | Not stated | 2025-07-30 | NCT05809635 | |
| Study of Human Ocular Hemodynamics by Holography Dopple | Arterial Occlusive Diseases, brain disorder, cardiovascular disorder, carotid artery disorder, carotid stenosis, central nervous system disorder, cerebrovascular disorder, eye disorder, glaucoma, nervous system disorder, ocular hypertension, retinal vascular disorder, vascular disorder | Not yet recruiting | Not applicable | 2025-05-25 | NCT06989996 | |
| oCular Examination at Cell RESolution With Optical TransmissionTomography | Glaucoma Associated With Other Ocular Disorders | Recruiting | Not applicable | 2025-05-16 | NCT06976034 | |
| Impact of Age-related Macular Degeneration on Daily Living Activitie | age-related macular degeneration, eye disorder, macular degeneration, retinal degeneration, retinal disorder | Not yet recruiting | Not applicable | 2024-03-27 | NCT06333873 | |
| Prospective CoHoRt Of Non-infectious Intermediate, pOsterior or panuveitiS | Non-infectious Uveitis | Not yet recruiting | Not applicable | 2023-07-03 | NCT05928754 | |
| Large Cohort of 1000 Patients With Severe Myopia | eye disorder, myopia, refractive error | Not yet recruiting | Not applicable | 2023-05-23 | NCT05849974 | |
| STReetlab Assessment Tool of Activities Daily Living in Glaucoma Patient | cranial nerve neuropathy, eye disorder, nervous system disorder, optic nerve disorder | Not yet recruiting | Not applicable | 2023-02-28 | NCT05747781 | |
| 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 |