Actively Recruiting

All Genders
NCT07482228

Long-term Clinical Outcomes After Retinal Artery Occlusion

Led by Chonnam National University Hospital · Updated on 2026-03-19

15000

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Retinal artery occlusion (RAO) is a rare but vision-threatening vascular disorder that is commonly caused by embolic events originating from the heart or carotid arteries. Patients with RAO are known to have an increased risk of subsequent cardiovascular and cerebrovascular events, including ischemic stroke and myocardial infarction. However, long-term outcomes and optimal medical treatment strategies for these patients remain insufficiently characterized. The purpose of this nationwide population-based study is to investigate the incidence of long-term cardiovascular and cerebrovascular outcomes in patients diagnosed with retinal artery occlusion using the Korean National Health Insurance Service (NHIS) database. In addition, the study aims to evaluate the impact of various medical therapies, including antiplatelet agents, anticoagulants, and statins, on long-term clinical outcomes.

CONDITIONS

Official Title

Long-term Clinical Outcomes After Retinal Artery Occlusion

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients newly diagnosed with retinal artery occlusion
Not Eligible

You will not qualify if you...

  • Patients with a prior diagnosis of retinal artery occlusion before the study period.
  • Patients diagnosed with giant cell arteritis.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chonnam National University Hospital

Gwangju, Gwangju, South Korea, 61469

Actively Recruiting

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Research Team

S

Seung Hun Lee, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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