Clinical trial Recruiting at 1 site Observational Ages 18 and up

Measuring retinal blood vessel density in patients with microvascular angina

Official title: The Value of Measuring Retinal Vascular Density by Optical Coherence Tomography-Angiography (OCT-A) in Patients With Microvascular Angina Confirmed by Myocardial Microcirculatory Resistance Index (MRI).

Run by Centre Hospitalier Universitaire Dijon · NCT06692751 · Data updated 2026-11-12

This study is testing whether a new eye scan can help doctors see if people with microvascular angina have issues with blood flow in their hearts without needing invasive procedures.

More Microvascular Angina trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment52 (estimated)
SponsorCentre Hospitalier Universitaire Dijon
Academic / other
Locations1 site (Dijon)
StatusRecruiting
StartedNovember 13, 2024
Main results expectedNovember 2029
Study endsNovember 2029
Registry record updatedOctober 22, 2026
Trial IDNCT06692751 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults diagnosed with microvascular angina who have undergone an MRI measurement and have no significant coronary artery lesions.

Probably not a fit

Patients with significant coronary artery lesions, severe retinal pathology, or those unable to provide consent may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the use of Optical Coherence Tomography-Angiography (OCT-A) to measure retinal vascular density in patients diagnosed with microvascular angina, a condition characterized by impaired blood flow in the heart's microcirculation. The study aims to provide a non-invasive and cost-effective alternative to the invasive measurement of microcirculatory resistance index (MRI) for diagnosing this condition. By correlating retinal microcirculation with cardiac health, the research seeks to enhance diagnostic accuracy and patient management. Participants will undergo blood sampling, ophthalmological examinations, and complete an angina severity questionnaire.

Why it matters

Potential benefit: If successful, this approach could lead to improved diagnosis and management of microvascular angina, benefiting millions of patients worldwide.

How similar studies have gone: Previous studies have indicated a correlation between retinal microcirculation and cardiovascular risk, suggesting potential success for this novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients managed at Dijon University Hospital, having had an IMR measurement as part of INOCA during a coronary angiographic examination, consecutively includible, without angiographically or functionally significant coronary epicardial lesion (FFR \< 0.80) explaining the clinical picture (= INOCA)
* Person having given oral consent
* Adult

Exclusion Criteria:

* Person not affiliated or not benefiting from a social security scheme
* Person subject to a legal protection measure (curatorship, guardianship) or a safeguard of justice measure
* Pregnant or breast-feeding women
* An adult incapable or unable to give consent
* Person with macular or retinal pathology, or severe bilateral myopia
* Person with genetic or idiopathic cardiomyopathy (dilated, hypertrophic or restrictive cardiomyopathy)

Where it's running

  • CHU Dijon Bourgogne
    Dijon, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.