NCT01053858已完成不适用
Triamcinolone or Bevacizumab for Central Retinal Vein Occlusion With Poor Vision
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 38
- 试验地点
- 2
- 主要终点
- best corrected visual acuity
研究概览
简要总结
To evaluate the effect of intravitreal bevacizumab with intravitreal triamcinolone for the treatment of central retinal vein occlusion (CRVO) presenting poor visual acuity.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •central macular thickness of more than 250 μm and baseline visual acuity of 20/200 or worse than 20/200 in patient with central retinal vein occlusion
排除标准
- •previous treatment such as intravitreal injection, subtenon injection, or laser photocoagulation since the time of onset
- •Patients with a history of glaucoma, neovascular glaucoma, diabetic retinopathy, and macular disorders
- •neovascularization on the disc or elsewhere or rubeosis
结局指标
主要结局
best corrected visual acuity
时间窗: baseline, 1 month, 2 months, 3 months, 6 months, 12 months
次要结局
- central macular thickness by optical coherence tomography(baseline, 1 month, 2 months, 3 months, 6 months 12months)
研究者
研究点 (2)
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