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Clinical Trials/NCT02215109
NCT02215109
Completed
Not Applicable

Change of Retinal Vessel Diameter in Branch Retinal Vein Occlusion After Intravitreal Bevacizumab Injection

Kyungpook National University Hospital1 site in 1 country25 target enrollmentApril 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Branch Retinal Vein Occlusion
Sponsor
Kyungpook National University Hospital
Enrollment
25
Locations
1
Primary Endpoint
Unoccluded retinal vessel diameter of Branch Retinal Vein Occlusion
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The authors investigated the consecutive change of retinal vessel's diameter in affected eye and fellow eye of Branch Retinal Vein Occlusion.

Detailed Description

Twenty five consecutive patients who had undergone intravitreal bevacizumab injection for Branch Retinal Vein Occlusion with macular edema were included in this study. All subjects were enrolled between April, 2012 and April, 2013 in the Department of Ophthalmology, Kyungpook National University Hospital.

Registry
clinicaltrials.gov
Start Date
April 2012
End Date
August 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dong Ho Park

Clinical professor

Kyungpook National University Hospital

Eligibility Criteria

Inclusion Criteria

  • Best-corrected visual acuity less than 20/40
  • Central subfield macular thickness (CSMT) 300 μm or greater on spectral-domain optical coherence tomography

Exclusion Criteria

  • Patients with recurrent BRVO
  • History of previous treatments for BRVO including vitreoretinal surgery, intravitreal injection, subtenon injection or laser photocoagulation
  • Patients with diabetes or dyslipidemia
  • IOP ≥ 22mmHg, treatment for glaucoma, a family history of glaucoma, or optic neuropathy
  • High myopia (\<-6 Diopters), high hyperopia (\>6 Diopters) or a history of refractive surgeries
  • Co-existing retinal disease other than BRVO
  • Corneal diseases include ulcer, keratoconus and a history of corneal laceration
  • Cataract and other media opacities resulting in visual impairment or poor fundus images

Outcomes

Primary Outcomes

Unoccluded retinal vessel diameter of Branch Retinal Vein Occlusion

Time Frame: 0, 1, 3, and 6 months

To evaluate the change of unoccluded retinal vessel diameter in affected eye of Branch Retinal Vein Occlusion and unaffected fellow eye.

Study Sites (1)

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