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临床试验/NCT00370851
NCT00370851已完成3 期

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

Shahid Beheshti University of Medical Sciences1 个研究点 分布在 1 个国家目标入组 82 人开始时间: 2006年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
82
试验地点
1
主要终点
Best corrected visual acuity

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with acute BRVO with less than three month duration

排除标准

  • 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

研究组 & 干预措施

1

Experimental

Intravitreal injection of Avastin

干预措施: Avastin (Bevacizumab) (Drug)

2

Sham Comparator

干预措施: Avastin (Bevacizumab) (Drug)

结局指标

主要结局

Best corrected visual acuity

时间窗: At 12 week

Macular thickness by OCT

时间窗: At 12 week

次要结局

  • Need for macular photocuagulation(At 12th week)
  • Incidence of new vessel formation(At 12th week)

研究者

研究点 (1)

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