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临床试验/NCT00661583
NCT00661583已完成1 期

Occlusion Prevention for Trabeculectomy Procedures Using Combination Ranibizumab and Mitomycin C (MMC) During Surgery (OCTOPUS Study)

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2008年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
30
试验地点
1
主要终点
Assessment of Ocular Adverse Events

研究概览

简要总结

The purpose of the study is to study the safety of the combination of ranibizumab and MMC vs monotherapy MMC vs intravitreal ranibizumab injection in patients with glaucoma.

详细描述

A common problem after undergoing trabeculectomy surgery to create a bleb (blister or bubble) to reduce intraocular pressure, is scarring of the opening. This scarring prevents fluid drainage and interferes with the proper functioning of the bleb. MMC (Mitomycin C) is usually administered intraoperatively, to reduce scarring and increase filtration. However, the failure rate of trabeculectomy remains high. Anti-VEGF (Vascular endothelial growth factor) agents have been used successfully in cases requiring bleb needling. The purpose of the study is to determine the safety of the combination of ranibizumab and MMC vs monotherapy MMC in patients with glaucoma.

This is an open-label, Phase I/II safety study of 30 patients randomized to either treatment with ranibizumab 0.5 mg intravitreally injected (n=10), combination ranibizumab 0.5mg intravitreally injected and MMC (0.4 mg/ml for 2 min) in eyes after trabeculectomy (n=10) or MMC therapy alone (n=10).

For the ranibizumab groups, a repeat injection of ranibizumab 0.5mg may be given PRN (as needed) at 1 month if hypervascularity or neovascularization of the conjunctiva exists.

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
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • undergoing trabeculectomy
  • 21 years of age or older

排除标准

  • pregnancy or lactation
  • any condition the investigator believes would impose a significant hazard to the patient if investigational therapy were initiated
  • history of ocular surface disease
  • cataract surgery in the past 6 months
  • history of active inflammatory, infectious or idiopathic keratitis

研究组 & 干预措施

Ranibizumab alone

Experimental

Treatment with ranibizumab 0.5 mg intravitreally injected (n=10)

干预措施: Ranibizumab (Drug)

Ranibizumab and MMC

Experimental

Combination ranibizumab 0.5mg intravitreally injected and MMC (0.4 mg/ml for 2 min) in eyes after trabeculectomy (n=10)

干预措施: Ranibizumab and MMC (Drug)

MMC alone

Active Comparator

MMC therapy alone (n=10)

干预措施: MMC (Drug)

结局指标

主要结局

Assessment of Ocular Adverse Events

时间窗: 6 months

To assess ocular adverse events of combination ranibizumab and MMC therapy at 6 months

次要结局

  • Percent of Subjects With a Qualified Success and Viable Bleb at 6 Months.(6 months)
  • Mean Change in in Intraocular Pressure.(6 months)
  • Mean Change in Visual Acuity(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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