Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05294978

EyeConic: Qualification for Cone-Optogenetics

Qualification for Cone-Optogenetics (EyeConic)

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Institute of Molecular and Clinical Ophthalmology Basel · Academic / Other
Sex
All
Age
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTOptical coherence tomography (OCT)Data of macular optical coherence tomography (OCT)

Timeline

Start date
2021-07-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2022-03-24
Last updated
2025-07-31

Locations

9 sites across 7 countries: United States, China, Germany, Hungary, Italy, Switzerland, United Kingdom

Source: ClinicalTrials.gov record NCT05294978. Inclusion in this directory is not an endorsement.