Eye test may reveal hidden heart risks
NCT ID NCT03739073
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether a non-invasive eye scan (OCTA) can predict how well blood flows in the heart's small arteries. Researchers examined 101 people with coronary artery disease, comparing eye images to measurements taken during heart catheterization. The goal was to see if the eye test could replace or reduce the need for invasive heart procedures.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple, non-invasive eye test to help assess heart artery health without invasive procedures.
- What could go wrong
- This is a small, early-stage study (101 participants) focused on finding a correlation, not proving a treatment. The results may not apply to all patients or lead to a reliable test.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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101 people
The number who actually took part.
- Started
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Oct 2018
- Finished
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Mar 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male and female patient's ≥18 years of age with coronary arterial indication as usual and with proximal and / or mean IVA stenosis ≥ 50%. 2. Signed informed consent 3. Affiliation to the social security system Exclusion Criteria: 1. Unstable Coronary Artery Disease 2. Atrial fibrillation 3. History of myocardial infarction \<6 months in the territory of the proximal and / or mean IVA. 4. Asthma 5. Aortocoronary bypass surgery. 6. Collateral development at the level of the proximal and / or mean IVA. 7. Allergy to iodine, severe renal insufficiency. 8. Ametropia\> = 6 diopters. 9. History of retinal ocular pathologies other than uncomplicated diabetic retinopathy and hypertensive retinopathy. 10. History of ophthalmic treatments such as macular or panretinal laser photocoagulation, intravitreal injection of anti-VEGF or cortisone. 11. Chronic glaucoma 12. Patients under guardianship or curators. 13. Pregnant or lactating women. 14. Patient's not affiliated to the French social security. 15. Persons placed under the protection of justice, 16. Subject participating in another research including an exclusion period still in progress at pre-inclusion
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hospices Civils de Lyon - Hopital de la Croix Rousse
Lyon, 69004, France
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