Correlating the Measure of Retinal Vascular Density Through Angio-OCT with Calcium Score

NCT ID: NCT05624255

Last Updated: 2024-11-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

101 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-15

Study Completion Date

2023-03-16

Brief Summary

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Recent case-control studies have proven that the retinal vascularization mirrors the cardiac vascularization: more the coronary network is altered, more the density of retinal vessels is reduced. No studies have yet been realised in primary prevention. This study aims to demonstrate a link between the density of the retinal vascularization and the calcium score, which is currently the gold standard for the classification of cardiovascular risk in primary prevention. Thus, a simple image of the retinal vascularization could predict the cardiovascular risk of a patient. OCT angiography would become a major aid in the classification of cardiovascular risk in asymptomatic patients.

Detailed Description

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Conditions

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Cardiovascular Abnormalities Vascular Diseases Retinal Vascular

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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ophthalmology consultation

Patients eligible to calcium score will be offered an ophthalmologic consultation including Angio-Optical Coherence Tomography \[OCT\]

Group Type EXPERIMENTAL

Ophthalmologic consultation

Intervention Type OTHER

Complete ophthalmologic examination including angio-OCT

Interventions

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Ophthalmologic consultation

Complete ophthalmologic examination including angio-OCT

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients eligible for a calcium score as part of their standard treatment and volunteers for an ophthalmologic consultation

Exclusion Criteria

* Pregnant women
Minimum Eligible Age

40 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Besancon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU de Besançon

Besançon, , France

Site Status

Countries

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France

Other Identifiers

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2022/701

Identifier Type: -

Identifier Source: org_study_id

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