Actively Recruiting

All Genders
Healthy Volunteers
ID05294978

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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - About 10 minutes

Participants undergo macular optical coherence tomography (OCT) imaging to assess retinal structure and volume.

1 visit (in-person)

Long-term Monitoring

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

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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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