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EyeConic: Qualification for Cone-Optogenetics

Sponsor: Institute of Molecular and Clinical Ophthalmology Basel

NCT ID: NCT05294978

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Optical coherence tomography (OCT) (diagnostic test)
How long the study runs
Study runs about 65 months (dates as stated)
About the drug or intervention
Optical coherence tomography (OCT) — diagnostic test: Data of macular optical coherence tomography (OCT)
Patient visit burden
Not specified by the sponsor

In plain English

This study, run by the Institute of Molecular and Clinical Ophthalmology Basel, is looking at inherited retinal dystrophies, which are conditions that affect the light-sensitive tissue at the back of the eye. The study is about qualification for cone-optogenetics, an approach that may help vision. Not stated — ask the trial team about the full aims and how the treatment works.

Who can take part

  • Patients: a diagnosis of a generalised inherited retinal disease (a condition affecting the retina that runs in families).
  • Patients: low vision in the study eye, meaning eyesight at or worse than 0.05 (or 20/400) on a vision chart.
  • Patients: able to have a macular optical coherence tomography (OCT) scan, which is a detailed picture of the central part of the retina.
  • Healthy controls: normal findings on eye checks.
  • Healthy controls: able to have a macular OCT scan.

Who may not be able to

  • Anyone with other eye diseases that significantly affect eyesight or the structure of the retina.
  • Anyone with a condition outside the eye that affects the retina, such as a neurodegenerative disease.

What taking part involves

  • • Not stated — ask the trial team about what tests or procedures are involved.

Time commitment: Not stated — ask the trial team about visits, how long the study lasts, and what taking part involves.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
Not specified
Who
All
Number of participants
1,000
Started
2021-07-01
Last checked
2025-07

Plain English Summary

What is this study?

  • • Testing a new treatment for retinal dystrophies
  • • Clinical study - 1,000 participants
  • • This study aims to prepare for the first-in-human clinical trial of cone optogenetics vision restoration

Who can take part?

  • • Adults
  • • Diagnosed with retinal dystrophies

Where?

  • • London - Moorfields Eye Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

More detail

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.

Retinal Dystrophies

How this trial compares with your answers

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What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: Not specified
  • Who can join: All genders

What the study is looking for

  • ✓Inclusion Criteria (patients):
  • ✓Diagnosis of generalized IRD
  • ✓Low vision as defined as visual acuity worse or equal to 0.05 (or 20/400) in the study eye
  • ✓Availability of macular optical coherence tomography (OCT)
  • ✓Inclusion Criteria (controls):
See the full criteria
Inclusion Criteria (patients): * Diagnosis of generalized IRD * Low vision as defined as visual acuity worse or equal to 0.05 (or 20/400) in the study eye * Availability of macular optical coherence tomography (OCT) Inclusion Criteria (controls): * Normal ophthalmic findings * Availability of macular optical coherence tomography (OCT) Exclusion Criteria (all): * Other eye diseases with a significant effect on vision or retinal structure * Extraocular disease affecting retinal structure such as neurodegenerative diseases

Where Is This Study? (1 UK site)

Moorfields Eye Hospital

London, United Kingdom

Recruiting
Site contact (verified)
Michel Michalides, MDPrincipal Investigator

How to Get in Touch

Lucas Janeschitz-Kriegl, MD

Sponsor contact

CONTACT

+41787494373 lucas.janeschitz@iob.ch

Tiana Koottungal

Sponsor contact

CONTACT

+41788486737 tiana.koottungal@iob.ch
Data sourced from ClinicalTrials.gov · Last verified: 2025-07