cone dystrophy
cone dystrophy
Explore linked clinical trials. Standard reference: MONDO:000045517 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Vulvodynia Intervention: the Effect of Multimodal Treatment for Provoked Vulvodynia | Chronic Pain, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Neurologic Manifestations, Pain, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Urogenital Diseases, color vision disorder, cone dystrophy, eye disorder, female reproductive system disorder, nervous system disorder, vision disorder, vulvar disease, vulvodynia | Active, not recruiting | Not applicable | 2026-08-12 | NCT06981611 | |
| Optilume™ BPH Catheter System in Men With Symptomatic BPH | Eye Diseases, Hereditary, Genital Diseases, Male Urogenital Diseases, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Urogenital Diseases, benign prostatic hyperplasia, color vision disorder, cone dystrophy, eye disorder, male reproductive system disorder, nervous system disorder, prostate disorder, vision disorder | Active, not recruiting | Not applicable | 2026-07-30 | NCT04131907 | |
| Naturally Produced Cannabinoids for Neuroprotection From Concussion | Brain Concussion, Brain Injuries, Traumatic, Chemically-Induced Disorders, Craniocerebral Trauma, Eye Diseases, Hereditary, Head Injuries, Closed, Inflammation, Neurologic Manifestations, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Wounds, Nonpenetrating, brain disorder, brain injury, cannabis dependence, central nervous system disorder, color vision disorder, cone dystrophy, eye disorder, injury, nervous system disorder, nervous system injury, psychiatric disorder, substance-related disorder, vision disorder | Recruiting | Phase 2 | 2026-07-21 | NCT07715864 | |
| Imaging Studies in Corticobasal Syndrome | Eye Diseases, Hereditary, Nerve Degeneration, Neurologic Manifestations, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, corticobasal degeneration disorder, eye disorder, nervous system disorder, neurodegenerative disease, tauopathy, vision disorder | Recruiting | Not stated | 2026-07-14 | NCT07000851 | |
| Stem Cell Ophthalmology Treatment Study II | Abnormalities, Multiple, CNS demyelinating autoimmune disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Injuries, Craniocerebral Trauma, Deaf-Blind Disorders, Deafness, Doyne honeycomb retinal dystrophy, Ear Diseases, Eye Diseases, Hereditary, Geographic Atrophy, Hearing Loss, Sensorineural, Leber hereditary optic neuropathy, Neurologic Manifestations, Nutritional and Metabolic Diseases, Optic Atrophy, Autosomal Dominant, Optic Neuropathy, Ischemic, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Stargardt disease, Usher syndrome, Vision, Low, acute transverse myelitis, age-related macular degeneration, autoimmune disease, autoimmune disorder of the nervous system, blindness (disorder), cardiovascular disorder, cone dystrophy, cone-rod dystrophy, cranial nerve neuropathy, demyelinating disease, eye disorder, glaucoma, hearing disorder, hearing loss disorder, hereditary disease, hereditary optic atrophy, immune system disorder, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, inherited retinal dystrophy, injury, macular degeneration, metabolic disease, nervous system disorder, nervous system injury, neurodegenerative disease, neuromyelitis optica, nutritional deficiency disease, nutritional disorder, ocular hypertension, optic atrophy, optic nerve disorder, optic neuritis, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, traumatic optic neuropathy, vascular disorder, vision disorder, vitamin A deficiency, vitamin deficiency disorder, wet macular degeneration | Recruiting | Not applicable | 2026-06-29 | NCT03011541 | |
| Alcohol Use Disorder and Cannabidiol | Alcohol Use Disorder, Chemically-Induced Disorders, Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, alcohol-related disorders, cannabis dependence, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, psychiatric disorder, substance-related disorder, vision disorder | Recruiting | Phase 2 / Phase 3 | 2026-06-15 | NCT05613608 | |
| 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 | |
| Adaptive Optics Imaging of Outer Retinal Diseases | 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, Rod-Cone Dystrophy, Sensation Disorders, Signs and Symptoms, Usher syndrome, age-related macular degeneration, blindness (disorder), cone dystrophy, cone-rod dystrophy, eye disorder, hearing disorder, hearing loss disorder, hereditary disease, inherited retinal dystrophy, late-onset retinal degeneration, macular degeneration, nervous system disorder, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorder | Recruiting | Not stated | 2026-05-08 | NCT05355415 | |
| The Effect of Emotional Freedom Techniques (EFT) in Smokers Failing a Smoking Cessation Program | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, eye disorder, injury, nervous system disorder, vision disorder | Recruiting | Early phase 1 | 2026-04-27 | NCT00981396 | |
| Topical CBD Scar Outcomes Study | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, eye disorder, injury, nervous system disorder, vision disorder | Not yet recruiting | Early phase 1 | 2026-04-01 | NCT05650697 | |
| Analysis of the Therapeutic and Clinical Profile of Cannabinoid Treatments: A Real-World Study | Chemically-Induced Disorders, Chronic Pain, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytopenia, Eye Diseases, Hereditary, Hemic and Lymphatic Diseases, Neurologic Manifestations, Pain, Pathological Conditions, Signs and Symptoms, Primary Immunodeficiency Diseases, Sensation Disorders, Signs and Symptoms, Wiskott-Aldrich syndrome, X-linked disease, anxiety disorder, blood coagulation disease, cannabis dependence, color vision disorder, cone dystrophy, eye disorder, hematologic disorder, hemorrhagic disease, hereditary disease, immune system disorder, inborn error of immunity, inherited blood coagulation disorder, leukocyte disorder, leukopenia, lymphopenia, nervous system disorder, psychiatric disorder, substance-related disorder, vision disorder | Enrolling by invitation | Not stated | 2026-03-30 | NCT07362407 | |
| Natural History Study of Inherited Retinal Diseases | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, achromatopsia, color vision disorder, cone dystrophy, eye disorder, inherited retinal dystrophy, macular degeneration, nervous system disorder, retinal degeneration, retinal disorder, vision disorder | Recruiting | Not stated | 2025-12-10 | NCT07085533 | |
| RCT of CBT Based C.A.T Project for Pakistani Adolescents With Anxiety Disorders. | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, vision disorder | Active, not recruiting | Not applicable | 2025-10-02 | NCT07202715 | |
| Study of Visual Perception Phenomena: Phosphene Mapping Induced by TMS and Its Relationship With Eye Movements | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, vision disorder, visual snow syndrome | Recruiting | Not applicable | 2025-08-07 | NCT07110493 | |
| Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Bowel | Constriction, Pathologic, Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, vision disorder | Recruiting | Phase 3 | 2025-06-25 | NCT05561127 | |
| Treating Suicidality Remotely | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, vision disorder | Recruiting | Not applicable | 2024-05-20 | NCT06370104 | |
| Safety and Efficacy of rAAV.hCNGA3 Gene Therapy in Patients With CNGA3-linked Achromatopsia | Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, achromatopsia, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, vision disorder | Active, not recruiting | Phase 1 / Phase 2 | 2024-04-18 | NCT02610582 |