choroideremia
choroideremia
Explore linked clinical trials. Standard reference: MONDO:00105577 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Inherited Retinal Degenerative Disease Registry | Abnormalities, Multiple, Bardet-Biedl syndrome, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Charcot-Marie-Tooth disease, Chronic Disease, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Disease Attributes, Dyslipidemias, Ear Diseases, Eye Diseases, Hereditary, Goldmann-Favre syndrome, Hearing Loss, Sensorineural, Juvenile Macular Degeneration, Kearns-Sayre syndrome, Leber congenital amaurosis, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Neurologic Manifestations, Neuronal Ceroid-Lipofuscinoses, Nutritional and Metabolic Diseases, Ocular Motility Disorders, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Peroxisomal Disorders, Rod-Cone Dystrophy, Sensation Disorders, Signs and Symptoms, Stargardt disease, Usher syndrome, X-linked disease, abetalipoproteinemia, achromatopsia, achromatopsia 3, adult Refsum disease, blindness (disorder), brain disorder, cardiomyopathy, cardiovascular disorder, central areolar choroidal dystrophy, central nervous system disorder, central nervous system malformation, choroideremia, color vision disorder, cone dystrophy, cone-rod dystrophy, congenital stationary night blindness, cranial nerve neuropathy, enhanced S-cone syndrome, eye disorder, fundus albipunctatus, hearing disorder, hearing loss disorder, heart disorder, hereditary disease, hereditary motor and sensory neuropathy, hypobetalipoproteinemia, hypolipoproteinemia, hypothalamic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, inherited neurodegenerative disorder, inherited retinal dystrophy, juvenile neuronal ceroid lipofuscinosis, lysosomal lipid storage disorder, macular degeneration, metabolic disease, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, ophthalmoplegia, optic choroid disorder, ornithine aminotransferase deficiency, otorhinolaryngologic disease, palsy, peripheral nervous system disorder, polyneuropathy, progressive external ophthalmoplegia, retinal degeneration, retinal disorder, retinitis pigmentosa, retinitis punctata albescens, retinoschisis, uveal disorder, vision disorder, vitelliform macular dystrophy | Recruiting | Not stated | 2026-05-19 | NCT02435940 | |
| High Resolution Retinal Imaging | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Geographic Atrophy, X-linked disease, age-related macular degeneration, choroideremia, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, optic choroid disorder, retinal degeneration, retinal disorder, retinitis pigmentosa, uveal disorder | Recruiting | Not stated | 2026-05-05 | NCT01866371 | |
| Study to Evaluate Safety of RTx-015 Injection in Retinitis Pigmentosa or Choroideremia Patients (ENVISION) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, X-linked disease, choroideremia, eye disorder, hereditary disease, inherited retinal dystrophy, optic choroid disorder, retinal degeneration, retinal disorder, retinitis pigmentosa, uveal disorder | Active, not recruiting | Phase 1 | 2026-02-20 | NCT06460844 | |
| HYPER MIND - Hyperoxia Effects on Cerebral Hemodynamics | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Critical Illness, Disease Attributes, Eye Diseases, Hereditary, Hyperoxia, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Signs and Symptoms, Respiratory, X-linked disease, choroideremia, eye disorder, hereditary disease, optic choroid disorder, uveal disorder | Recruiting | Not applicable | 2026-01-29 | NCT07377162 | |
| Dose Escalation Study of Intravitreal 4D-110 in Patients With Choroideremia | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, X-linked disease, choroideremia, eye disorder, hereditary disease, optic choroid disorder, uveal disorder | Active, not recruiting | Phase 1 | 2025-05-22 | NCT04483440 | |
| Observational Study to Assess Endpoint Operational Feasibility & Measurement Properties in Patients with Retinal Degeneration | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, X-linked disease, choroideremia, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, optic choroid disorder, retinal degeneration, retinal disorder, retinitis pigmentosa, uveal disorder | Recruiting | Not stated | 2025-01-08 | NCT06375239 | |
| Longitudinal Study of a Bionic Eye | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, X-linked disease, choroideremia, eye disorder, hereditary disease, inherited retinal dystrophy, optic choroid disorder, retinal degeneration, retinal disorder, retinitis pigmentosa, uveal disorder | Enrolling by invitation | Not stated | 2024-08-23 | NCT05158049 |