Actively Recruiting
Qualification for Cone-Optogenetics (EyeConic)
Led by Institute of Molecular and Clinical Ophthalmology Basel · Updated on 2025-07-31
1000
Participants Needed
9
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on inherited retinal dystrophies (IRDs), a group of eye conditions where cone cells in the retina lose their ability to sense light but may remain alive in a dormant state. The study aims to prepare for the first human trial of cone optogenetics, a technique to restore vision by reactivating these dormant cones. To do this, researchers are conducting a worldwide multicenter imaging study called EyeConic to identify eligible patients and estimate how many low vision patients have remaining cone cells. The study uses macular optical coherence tomography (OCT), a detailed imaging method of the retina, to gather data from both patients with IRDs and control participants with normal eye health. This observational study involves collecting and analyzing OCT images to assess central retinal volume and identify the presence of dormant cones. No treatments or interventions are given, as the study focuses on imaging and data collection. Participants will undergo OCT imaging to measure their retinal structure, particularly central retinal volume, which is the primary outcome. Researchers will review this baseline data to understand the proportion of patients with surviving cone cells. The study includes both patients with low vision due to IRDs and healthy controls. Participation involves one imaging session lasting about 10 minutes. The study is ongoing with an expected completion by December 2026.
CONDITIONS
Brief Title
EyeConic: Qualification for Cone-Optogenetics
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of generalized inherited retinal dystrophy (IRD)
- Low vision defined as visual acuity worse or equal to 0.05 (20/400) in the study eye
- Availability of macular optical coherence tomography (OCT) imaging
- Normal ophthalmic findings for control participants
- Availability of macular optical coherence tomography (OCT) imaging for controls
You will not qualify if you...
- Other eye diseases significantly affecting vision or retinal structure
- Extraocular diseases affecting retinal structure such as neurodegenerative diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - About 10 minutes
Participants undergo macular optical coherence tomography (OCT) imaging to assess retinal structure and volume.
1 visit (in-person)
Duration - Up to study completion
Participants are observed to estimate the proportion of low vision patients with remaining cone cell bodies.
Visit schedule varies depending on individual assessment
Trial Site Locations
Total: 9 locations
1
University of California San Francisco, Department of Ophthalmology
San Francisco, California, United States, 94158
Actively Recruiting
2
Bascom Palmer Eye Institute
Miami, Florida, United States, 33136
Actively Recruiting
3
University of Pittsburgh, Department of Ophthalmology
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
4
Beijing Institute of Ophthalmology
Beijing, China
Actively Recruiting
5
Universitätsklinikum Tübingen Augenklinik
Tübingen, Germany
Actively Recruiting
6
Semmelweis University, Department of Ophthalmology
Budapest, Hungary
Actively Recruiting
7
Oculista Ospedale Parma
Parma, Italy
Actively Recruiting
8
University Hospital Basel, Eye Clinic
Basel, Switzerland, 4031
Actively Recruiting
9
Moorfields Eye Hospital
London, United Kingdom
Actively Recruiting
Research Team
L
Lucas Janeschitz-Kriegl, MD
T
Tiana Koottungal
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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