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Deafness

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Deafness

Explore clinical trials studying Deafness. Study availability and eligibility vary by location and protocol.

37 public trials 11 recruiting studies

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Deafness trial results

Recruiting

A Study to Investigate the Safety of OpCT-001 in Adults Who Have Primary Photoreceptor Disease (CLARICO)

NCT06789445

Conditions: Abnormalities, Multiple, Blindness, Cone-Rod Disease (C-RD), +31 more
Locations: University of Southern California /Children's Hospital of Los Angeles Los Angeles, California, United States

University of Miami, Bascom Palmer Eye Institute Miami, Florida, United States

Mid Atlantic Retina/ Wills Eye Philadelphia, Pennsylvania, United States

Retina Foundation of the Southwest Dallas, Texas, United States

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Recruiting

Stem Cell Ophthalmology Treatment Study II

NCT03011541

Conditions: Abnormalities, Multiple, Age-Related Macular Degeneration, Autoimmune Diseases, +75 more
Locations: MD Stem Cells Westport, Connecticut, United States

MD Stem Cells Coral Springs, Florida, United States

MD Stem Cells Kobinia Med Vienna, Austria

The Saudi-German Hospital Dubai, United Arab Emirates

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Recruiting

Inherited Retinal Degenerative Disease Registry

NCT02435940

Conditions: Abetalipoproteinemia, Abnormalities, Multiple, Achromatopsia, +100 more
Locations: Foundation Fighting Blindness Columbia, Maryland, United States

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Recruiting

Adaptive Optics Imaging of Outer Retinal Diseases

NCT05355415

Conditions: Abnormalities, Multiple, Age-Related Macular Degeneration, Blindness, +31 more
Locations: NIH Clinical Center Bethesda, Maryland, United States

Food and Drug Administration Silver Spring, Maryland, United States

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Recruiting

Observational Study to Investigate the Short-term Effects of Transcorneal Electrical Stimulation on Visual Performance

NCT07548944

Conditions: Abnormalities, Multiple, Blindness, Cone Rod Dystrophy, +26 more
Locations: Augenzentrum Frankfurt Prof. Koch GmbH Frankfurt am Main, Germany

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Recruiting

Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset

NCT06475651

Conditions: Abnormalities, Multiple, Blindness, CHARGE Syndrome, +22 more
Locations: Department of Genomic Medicine for Rare Diseases and the Multidisciplinary Center for Prenatal Diagnosis of the Necker-Enfants malades Hospital Paris, France

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Recruiting

Natural History of Photoreceptor Degeneration in USH1B: Clinical Parameters and Validation of Functional Vision Tests in MYO7A

NCT07278843

Conditions: Abnormalities, Multiple, Blindness, Congenital Abnormalities, +23 more
Locations: Centre National d'Ophtalmologie des Quinze-Vingts Paris, Île-de-France Region, France

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Recruiting

Study of Subretinally Injected AAVB-081 in Patients With Usher Syndrome Type IB (USH1B) Retinitis Pigmentosa

NCT06591793

Conditions: Abnormalities, Multiple, Blindness, Congenital Abnormalities, +24 more
Locations: University of Campania Luigi Vanvitelli Naples, Italy

Moorfields Eye Hospital London, United Kingdom

Retina Clinic London London, United Kingdom

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Recruiting

Monogenic Diabetes Misdiagnosed as Type 1

NCT03988764

Conditions: Abnormalities, Multiple, Autoimmune Diseases, Blindness, +43 more
Locations: The Montreal Children's Hospital Montreal, Quebec, Canada

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Recruiting

GROWing Up With Rare GENEtic Syndromes

NCT04463316

Conditions: 17p- Deletiesyndrome, 1q25-32 Deletie, 22q11 Deletion Syndrome, +138 more
Locations: Erasmus Medical Center Rotterdam, South Holland, Netherlands

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Deafness

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