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Clinical Trials/NCT05082402
NCT05082402
Recruiting
Not Applicable

Imaging of Retinochoroidal Vasculature in Patients Being Assessed for Cardiovascular Disease

Northwestern University1 site in 1 country50 target enrollmentAugust 17, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Diseases
Sponsor
Northwestern University
Enrollment
50
Locations
1
Primary Endpoint
Correlation with and prediction of the presence/degree of carotid occlusive disease as determined by carotid duplex ultrasonography
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This study aims to determine whether changes in retinal vasculature seen on SS-OCTA can be correlated to degree of cardiovascular disease as measured by carotid duplex ultrasonography.

Detailed Description

The study's primary objective is to determine whether measures taken from SS-OCTA, color fundus photography, and retinal exams can correlate with and predict the presence/degree of carotid occlusive disease as determined by carotid duplex ultrasonography by examining the following parameters: retinal vessel caliber, retinal vessel density, retinal vessel perfusion, retinal vessel tortuosity, presence of Hollenhorst or other plaques, and/or areas of ischemia.

Registry
clinicaltrials.gov
Start Date
August 17, 2021
End Date
December 31, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rukhsana Mirza

Principal Investigator, M.D., MS

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Subjects between 18 and 80 years of age.
  • No known prior history of retinal disease.
  • Able to participate in a clinical eye examination setting.
  • Able to consent.
  • Subjects receiving standard of care carotid duplex ultrasounds.

Exclusion Criteria

  • Known ophthalmologic disease (e.g. glaucoma, macular degeneration, ocular injury) other than corrected refractive error.
  • Lack of capacity to provide informed consent.
  • Subjects younger than 18 years of age or older than 80 years of age.
  • History of stroke or acute loss of vision.
  • Unable to participate in a clinical eye examination setting.

Outcomes

Primary Outcomes

Correlation with and prediction of the presence/degree of carotid occlusive disease as determined by carotid duplex ultrasonography

Time Frame: 2 hours

Determining whether measures taken from SS-OCTA, color fundus photography, and retinal exams can correlate with and predict the presence/degree of carotid occlusive disease as determined by carotid duplex ultrasonography by examining the following parameters: retinal vessel caliber, retinal vessel density, retinal vessel perfusion, retinal vessel tortuosity, presence of Hellenhorst or other plaques, and/or areas of ischemia.

Study Sites (1)

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