EyeConic: Qualification for Cone-Optogenetics
Start Date
7/1/2021
Completion Date
12/1/2026
Summary
This study aims to prepare for the first-in-human clinical trial of cone optogenetics vision restoration. As a first step, this worldwide multicenter ocular imaging study (EyeConic Study) is performed to identify eligible patients.
Detailed Description
In a subset of patients with inherited retinal dystrophies (IRDs), cones lose their light-sensitive outer segments but remain alive in a dormant stage. This creates an opportunity to resensitize them through targeted optogenetic tools. However, the true proportion of low vision patients harboring dormant, non-functional cones, is currently unknown. The worldwide multicenter retrospective study (EyeConic) aims to estimate the proportion of low vision patients with remaining cone cell bodies for the first time.
Eligibility Criteria
Age Range: No minimum to No maximum
Interventions
Optical coherence tomography (OCT)
Conditions
Locations
University of California San Francisco, Department of Ophthalmology
San Francisco, California 94158
United States
Bascom Palmer Eye Institute
Miami, Florida 33136
United States
University of Pittsburgh, Department of Ophthalmology
Pittsburgh, Pennsylvania 15213
United States
Beijing Institute of Ophthalmology
Beijing,
China
Universitätsklinikum Tübingen Augenklinik
Tübingen,
Germany
Semmelweis University, Department of Ophthalmology
Budapest,
Hungary
Oculista Ospedale Parma
Parma,
Italy
University Hospital Basel, Eye Clinic
Basel, 4031
Switzerland
Moorfields Eye Hospital
London,
United Kingdom