跳至主要内容
临床试验/NCT01091896
NCT01091896Unknown2 期

Adjuvant Intravitreal Bevacizumab in Pars Plana Vitrectomy for Vitreous Hemorrhage Secondary to Diabetic Retinopathy

University of Sao Paulo1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
1
试验地点
1
主要终点
Recurrent vitreous hemorrhage incidence after vitrectomy

研究概览

简要总结

The purpose of this study is to determine the effect of pre and intra-operative bevacizumab injection on postoperative vitreous hemorrhage after diabetic vitrectomy in comparison to vitrectomy without bevacizumab injection.

详细描述

Postoperative vitreous hemorrhage is a common complication after vitrectomy for proliferative diabetic retinopathy. Bevacizumab (Avastin) is a potent inhibitor of angiogenesis and has been shown to decrease retinal and iris neovascularization in proliferative diabetic retinopathy. We believe that preoperative bevacizumab injection could reduce postoperative vitreous hemorrhage by decreasing the amount of abnormal vessels and intraoperative injection could also reduce postoperative vitreous hemorrhage by inhibiting the vessel formation after surgery

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • patients undergoing first vitrectomy for vitreous hemorrhage secondary to proliferative diabetic retinopathy

排除标准

  • follow-up period of less than 3 months
  • not first vitrectomy
  • abnormal blood coagulation
  • uncontrolled hypertension

研究组 & 干预措施

2- bevacizumab before vitrectomy

Experimental

Patients will receive intravitreal injection of 1.25 mg of bevacizumab (0.05 ml) 7 days before vitrectomy

干预措施: bevacizumab (Drug)

3- bevacizumab after vitrectomy

Experimental

Patients will receive intravitreal injection of 1.25 mg of bevacizumab (0.05 ml) at the end of vitrectomy

干预措施: bevacizumab (Drug)

结局指标

主要结局

Recurrent vitreous hemorrhage incidence after vitrectomy

时间窗: 3 months

次要结局

  • Visual outcome(3 months)

研究者

申办方类型
Other

研究点 (1)

Loading locations...

相似试验