跳至主要内容
临床试验/NCT03154892
NCT03154892已完成不适用

The Effect of Conbercept Injection Through Different Routes for Neovascular Glaucoma

Second Affiliated Hospital of Xi'an Jiaotong University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
NVI/NVA

研究概览

简要总结

The neovascular glaucoma (NVG) is a refractory type of secondary glaucoma and often lead to frustrated treatment and blindness. It has been confirmed high levels of vascular endothelial growth factor (VEGF) in NVG. Conbercept is an anti-VEGF agent,its role in regression of other neovascular disorders such as wet-type age-related macular degeneration and diabetic retinopathy has been described. Investigators aim to evaluate the efficacy and safety of intracameral and intravitreal injection of conbercept for the treatment of NVG.

详细描述

The neovascular glaucoma (NVG) is a refractory type of secondary glaucoma and often lead to frustrated treatment and blindness. It has been confirmed high levels of vascular endothelial growth factor (VEGF) in NVG. Conbercept is an anti-VEGF agent,Its role in regression of other neovascular disorders such as wet-type age-related macular degeneration and diabetic retinopathy has been described. The intravitreal injection of anti-VEGF agent has shown its therapeutic potential for the early stage of NVG, but not for the late stage. Intracameral injection maybe used as an alternative way for administration. Investigators aim to evaluate the efficacy and safety of intracameral and intravitreal injection of conbercept for the treatment of NVG.

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
None

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with a diagnosis of neovascular glaucoma (Stage 1-2-3)
  • Individuals who are ages 20-80 years old; male or female of chinese
  • Visual acuity of light perception or better in the study eye
  • Willing and able to comply with clinic visits and study-related procedures
  • Provide signed informed consent

排除标准

  • Use of intraocular anti-VEGF agents in the study eye in the past 3 months.
  • Active ocular or periocular infection in the study eye
  • Uncontrolled Blood Pressure
  • Thromboembolism
  • Congestive Heart Failure
  • Renal Failure
  • History of myocardial infarction
  • History of Stroke
  • Pregnant or breast-feeding women
  • Participation in another simultaneous medical investigator or trial

研究组 & 干预措施

Intracameral injection

Experimental

Intracameral injection of conbercept for the treatment of NVG

干预措施: Intracameral injection (Procedure)

Intravitreal injection

Active Comparator

Intravitreal injection of conbercept for the treatment of NVG

干预措施: Intravitreal injection (Procedure)

结局指标

主要结局

NVI/NVA

时间窗: 1 week and 1 month after operation

Changes in extent of iris or angle neovascularization

次要结局

  • IOP(1 week and 1 month after operation)
  • BCVA(1 week and 1 month after operation)

研究者

发起方
Second Affiliated Hospital of Xi'an Jiaotong University
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验