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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Follow-on Study for Second-Eye Treatment for Participants Previously Treated With Gene Therapy for X-Linked Retinitis Pigmentosa (XLRP)X-Linked Retinitis PigmentosaActive, not recruitingPhase 22026-09-25NCT06646289
Follow-up Gene Therapy Trial for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR GeneX-Linked Retinitis PigmentosaActive, not recruitingPhase 32026-09-25NCT04794101
A Study Investigating Subcutaneously Administered Pozelimab in Combination With Cemdisiran or Cemdisiran Alone in Adult Participants With Geographic AtrophyGeographic Atrophy, eye disorder, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 32026-09-18NCT06541704
Targeting Reactive Oxygen Species Production as a Novel Therapeutic in Fuch's Endothelial Corneal DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary diseaseRecruitingPhase 22026-09-02NCT04440280
A Study of AMG 732 in Healthy Participants and Participants With Thyroid Eye DiseaseCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Graves Ophthalmopathy, Graves disease, autoimmune disease, disease of orbital part of eye adnexa, endocrine system disorder, exophthalmos, eye disorder, goiter, hereditary disease, hyperthyroidism, immune system disorder, thyroid gland disorderActive, not recruitingPhase 1 / Phase 22026-08-10NCT06401044
Study of Remimazolam for Cataract SurgeryCataract Surgery AnesthesiaNot yet recruitingPhase 42026-07-15NCT07325227
A Registry of Subjects With Primary Indeterminate Lesions or Choroidal MelanomaNeoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Uveal Neoplasms, eye disorder, malignant choroid melanoma, melanocytic neoplasm, melanoma, neoplasm, neuroendocrine neoplasm, ocular cancer, primitive neuroectodermal tumor, uveal disorder, uveal melanomaActive, not recruitingNot stated2026-05-22NCT03941379
Outcomes Tracking in Unilateral Vocal Fold Paralysis (UVFP) and Atrophy After Medialization Laryngeal SurgeryNeurologic Manifestations, Paralysis, Unilateral, Vocal Cord, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Vocal Cord Paralysis, cranial nerve neuropathy, laryngeal disorder, nervous system disorder, otorhinolaryngologic disease, palsy, respiratory system disorder, vagus nerve disorderEnrolling by invitationNot stated2026-05-12NCT07579364
A Randomized Clinical Trial of Ex Vivo Corneal Cross-Linking of Donor Keratoplasty Tissue for Keratoconus Used for Keratoplasty in Keratoconus Patientscorneal disorder, eye disorder, keratoconusNot yet recruitingNot applicable2026-04-08NCT04584125
Dark Adaptation as an Early Indicator of Response to Statin Therapy for Intermediate AMDage-related macular degeneration, eye disorder, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 22026-01-26NCT04735263
Clinical Validation of DystoniaNet Deep Learning Platform for Diagnosis of Isolated DystoniaCraniomandibular Disorders, Cumulative Trauma Disorders, Dyskinesias, Jaw Diseases, Mandibular Diseases, Myoclonus, Neurologic Manifestations, Parkinson disease, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Sprains and Strains, Stomatognathic Diseases, Ulnar Nerve Compression Syndromes, Ulnar Nerve Entrapment Syndrome, arthropathy, basal ganglia disorder, brain disorder, central nervous system disorder, dystonic disorder, essential tremor, inherited torticollis, injury, laryngeal disorder, mononeuropathy, movement disorder, muscle tissue disorder, musculoskeletal system disorder, nerve compression syndrome, nervous system disorder, neurodegenerative disease, neurodevelopmental disorder, neuromuscular disease, otorhinolaryngologic disease, parkinsonian disorder, peripheral nervous system disorder, psychiatric disorder, respiratory system disorder, spasmodic dystonia, synucleinopathy, temporomandibular joint disorder, tic disorder, ulnar neuropathy, voice disordersRecruitingNot applicable2025-12-02NCT05317390
Brain-Computer Interfaces in Laryngeal DystoniaNeurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, laryngeal disorder, nervous system disorder, otorhinolaryngologic disease, respiratory system disorder, spasmodic dystonia, voice disordersRecruitingNot applicable2025-12-02NCT04421365
An fMRI Investigation of the Effects of IV Lidocaine on TinnitusEar Diseases, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, hearing disorder, hearing loss disorder, nervous system disorder, otorhinolaryngologic disease, tinnitusRecruitingEarly phase 12025-12-02NCT04192773
Imaging Genetics of Laryngeal DystoniaDyskinesias, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, dystonic disorder, laryngeal disorder, nervous system disorder, otorhinolaryngologic disease, respiratory system disorder, spasmodic dystonia, voice disordersRecruitingNot stated2025-12-02NCT03042975
A Study Of Lorlatinib Versus Crizotinib In First Line Treatment Of Patients With ALK-Positive NSCLCNeoplasms by Site, Thoracic Neoplasms, bronchial neoplasm, bronchogenic carcinoma, lung disorder, lung neoplasm, neoplasm, non-small cell lung carcinoma, respiratory system disorder, respiratory tract neoplasmActive, not recruitingPhase 32025-11-25NCT03052608
Efgartigimod for the Treatment of Acute Optic NeuritisCNS demyelinating autoimmune disease, acute transverse myelitis, autoimmune disease, autoimmune disorder of the nervous system, cranial nerve neuropathy, demyelinating disease, eye disorder, immune system disorder, multiple sclerosis, nervous system disorder, neuromyelitis optica, optic nerve disorder, optic neuritisRecruitingPhase 22025-11-10NCT06453694
An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 GeneCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingNot stated2025-09-19NCT06435000
A Phase 1/2, First-in-Human Dose Escalation/Expansion Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of a Subretinal Injection of SB-007 in Subjects With Stargardt Disease (STGD1)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 1 / Phase 22025-04-29NCT06942572