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Retinitis Pigmentosa

Clinical trial condition

Retinitis Pigmentosa

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

199 public trials 37 recruiting studies

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Retinitis Pigmentosa trial results

Recruiting

BS01 in Patients With Retinitis Pigmentosa

NCT04278131

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: New Jersey Retina Teaneck, New Jersey, United States

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Recruiting

High Resolution, High-speed Multimodal Ophthalmic Imaging

NCT04129021

Conditions: Brain Diseases, Cardiovascular Diseases, Central Nervous System Diseases, +36 more
Locations: Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts Paris, France

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Recruiting

The Effects of Disulfiram (Antabuse®) on Visual Acuity in Patients With Retinal Degeneration

NCT06319872

Conditions: Age-Related Macular Degeneration, Alcohol Use Disorder, Alcohol-Related Disorders, +14 more
Locations: Flaum Eye Institute, University of Rochester Medical Center Rochester, New York, United States

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Recruiting

Pilot Study of AuTNA I

NCT05853107

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: Chunhui Jiang Shanghai, Shanghai Municipality, China

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Recruiting

Study of BEST1 Vitelliform Macular Dystrophy

NCT05809635

Conditions: Best Vitelliform Macular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, +8 more
Locations: Columbia University Irving Medical Center New York, United States

Institut de la Vision/Centre de maladies rares du Centre Hospitalier National Ophtalmologique des Quinze-Vingts Paris, France

Eberhard Karls University Tubingen Tübingen, Germany

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Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

NCT01793168

Conditions: 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
Locations: Sanford Health Sioux Falls, South Dakota, United States

Online Patient Enrollment System Sydney, Australia

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Recruiting

InsightRP2 Registry

NCT06982417

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +8 more
Locations: University Medicine Göttingen Göttingen, Lower Saxony, Germany

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Recruiting

Safety and Efficacy of Stem Cell Small Extracellular Vesicles in Patients With Retinitis Pigmentosa

NCT06242379

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: Siriraj Hospital Bangkok Noi, Bangkok, Thailand

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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

An Open-label, Dose-ascending Study of IGT001 for Retinitis Pigmentosa

NCT06936787

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: Shanghai General Hospital, Shanghai Jiao Tong University Shanghai, China

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