跳至主要内容
临床试验/NCT01238393
NCT01238393已完成不适用

A Prospective Pilot Study of Lucentis for Epiretinal Membranes: the LERM Study

Queen's University1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2010年11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
11
试验地点
1
主要终点
Evidence of improvement measured by optical coherence tomography

研究概览

简要总结

The purpose of this study is to determine whether intraocular injection of ranibizumab decreases the retinal thickness in patients with epiretinal membranes and reduces associated symptoms.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • •symptomatic idiopathic epiretinal membrane

排除标准

  • •vision worse than 6/18 and fit for surgery
  • •prior vitreoretinal surgery or injection
  • •any past or current form of retinal vein occlusion or neovascularization
  • •age-related macular degeneration
  • •other condition causing significant limitation of visual potential

研究组 & 干预措施

Ranibizumab

Experimental

('intravitreal ranibizumab' )

干预措施: intravitreal ranibizumab (Drug)

结局指标

主要结局

Evidence of improvement measured by optical coherence tomography

时间窗: 3 and 6 months

次要结局

  • Subjective change in symptoms(3 and 6 months)
  • Amsler grid improvement(3 and 6 months)
  • Near visual acuity (Snellen)(3 and 6 months)
  • Distance visual acuity (ETDRS)(3 and 6 months)
  • Quality of life improvement(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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