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Clinical Trials/NCT03049514
NCT03049514CompletedNot Applicable

Study of Arterial Recanalization of the Central Retinal Artery Occlusions

Fondation Ophtalmologique Adolphe de Rothschild1 site in 1 country80 target enrollmentStarted: December 23, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
80
Locations
1
Primary Endpoint
Dynamic retinal angiography data at 24 hours (+/- 24 hours)

Study Overview

Brief Summary

Central retinal artery occlusions (CRAO) are the equivalent of an ischemic stroke (IS) at the retinal level. They share the same risk factors and common pathology. Their incidence is lower (8.5 / 100,000) and the functional prognosis is unfavorable in 80% of cases with visual acuity (VA) <1/10. The diagnosis of an CRAO is clinically based on the sudden occurrence of a decrease in deep visual acuity with fundamentally signs of reactive ischemia. There is no data on early retinal arterial recanalization after CRAO, nor on the relationship between early recanalization (spontaneous or post-thrombolysis) and visual prognosis.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Central Retinal Artery Occlusion ≤ 24 hours

Exclusion Criteria

  • Retinal Dynamic angiography not performed within 48 hours of onset of symptoms
  • Occlusion of a branch of the central retinal artery

Outcomes

Primary Outcomes

Dynamic retinal angiography data at 24 hours (+/- 24 hours)

Time Frame: 24 hours (+/- 24 hours) following the beginning of symptoms

Proportion of patients with early arterial recanalization.The recanalization rate will be compared between thrombolysed patients and non-thrombolysed patients

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Network
Responsible Party
Sponsor

Study Sites (1)

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