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Intravitreal Bevasizumab VS Sham Treatment in Acute BRVO: A Randomized Clinical Trial

Phase 3
Completed
Conditions
Retinal Disease
Interventions
Registration Number
NCT00370851
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

In this study we intend to evaluate the outcome of intravitreal avastin on improving the visual acuity and macular edema and late complications of BRVO like NVD and NVE

Detailed Description

After diabetic retinopathy, vein occlusion is the second most common retinovascular disease. According to BVO study the only effective management of it is macular photocoagulation for macular thickening that persist after 3 months.But we may miss a golden time which resulted to photoreceptor degeneration due to macular edema during this period. VEGF inhibitors newly have been shown that may be effective on a wide range of retinovascular diseases that resulted to macular edema or new vessels formation. In this study we aim to show the outcomes of one of this VEGF inhibitors (bevacizumab) on complications of BRVO in a sham controlled clinical trial.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
82
Inclusion Criteria
  • patients with acute BRVO with less than three month duration
Exclusion Criteria
  • vision less than 20/320 and vison more than 20/50
  • duration more than 3 months
  • history of glaucoma and diabetic retinopathy
  • any media opacity that prevent funduscopy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1Avastin (Bevacizumab)Intravitreal injection of Avastin
2Avastin (Bevacizumab)-
Primary Outcome Measures
NameTimeMethod
Best corrected visual acuityAt 12 week
Macular thickness by OCTAt 12 week
Secondary Outcome Measures
NameTimeMethod
Need for macular photocuagulationAt 12th week
Incidence of new vessel formationAt 12th week

Trial Locations

Locations (1)

Siamak Moradian, MD

🇮🇷

Tehran, Iran, Islamic Republic of

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