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临床试验/NCT01288404
NCT01288404已完成不适用

A Pilot Study of Subconjunctival Bevacizumab Injection in Impending Recurrent Pterygium

Ramathibodi Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
1
主要终点
Severity of impending recurrent pterygium

研究概览

简要总结

Hypothesis: Subconjunctival bevacizumab injection may potentially suppress neovascularization in pterygium, preventing or retarding the progression of recurrence.

详细描述

  1. Impending recurrent pterygium
  2. Anti-VEGF therapy
  • Bevacizumab
  • Subconjunctival injection
  • Suppress neovascularization

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Impending recurrent pterygium developed within 6 months following pterygium surgery either simple excision or excision with grafting.
  • Failure of conventional topical anti-inflammatory therapy for impending recurrent pterygium which was defined by the progression of fibrovascular tissue over the excised area despite receiving treatment.
  • No history of any adjunctive treatment such as MMC, 5-FU, periocular injection of corticosteroids and beta radiation.
  • No other ocular surface pathologies or coexisting ocular diseases.
  • No other ocular surgeries within the previous 6 months.
  • No history of allergy to the medications used in this study.
  • Good compliance with the study regimen and availability for the duration of the entire study period.

排除标准

  • Platelet disorders
  • Hypertension
  • Pregnant or lactating women

研究组 & 干预措施

Bevacizumab group 1

Active Comparator

Bevacizumab 1.25 mg/0.05mL

干预措施: Bevacizumab (Drug)

Control

Placebo Comparator

topical 0.1% fluorometholone eye drops

干预措施: Fluorometholone (Drug)

Bevacizumab group 2

Active Comparator

Bevacizumab 2.5 mg/0.1mL

干预措施: Bevacizumab (Drug)

bevacizumab group 3

Active Comparator

bevacizumab 3.75 mg/0.15mL

干预措施: Bevacizumab (Drug)

结局指标

主要结局

Severity of impending recurrent pterygium

时间窗: 3 months

次要结局

  • Visual analog scales(3 months)
  • Adverse reactions(3 months)

研究者

申办方类型
Other

研究点 (1)

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