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临床试验/NCT00665756
NCT00665756Unknown不适用

Comparison of Efficacy Between Silicone Ahmed Glaucoma Valves and Second Trabeculectomy in Glaucoma Patients

Federal University of São Paulo2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2006年1月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
40
试验地点
2
主要终点
intra ocular pressure

研究概览

简要总结

In the management of open angle glaucoma, frequently more then one procedure is necessary to control the intra ocular pressure. There is still no consensus whether this second intervention should be a second trabeculectomy or a shunt device. In the present study we compare a second trabeculectomy versus Ahmed silicone shunt device in open angle glaucoma patients with previous trabeculectomy without proper IOP control.

详细描述

In the management of open angle glaucoma, frequently more then one procedure is necessary to control the intra ocular pressure. There is still no consensus whether this second intervention should be a second trabeculectomy or a shunt device. In the present study we compare a second trabeculectomy versus Ahmed silicone shunt device in open angle glaucoma patients with previous trabeculectomy without proper IOP control.

40 Patients with clinically uncontrolled open angle glaucoma with previous trabeculectomy surgery were selected from the glaucoma sector of Federal university of Sao Paulo. Patients were randomized to one of two groups:

  1. Silicone Ahmed Implant
  2. Second trabeculectomy

Surgery description:

Ahmed silicone tube implant: A fornix-based conjunctival flap was created between two adjacent recti muscles. Before placement of the tube implant body to the sclera, tube was irrigated with saline solution to open the valve mechanism. The implant's polypropylene body was sutured to sclera with 6.0 silk suture. The tube then trimmed and the anterior chamber was entered from 1mm posterior to corneoscleral limbus with 23-gauge needle. A human donor scleral flap was placed over the tube and sutured to the sclera with 10.0 nylon suture. The conjunctiva was sutured to the limbus.

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
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with open angle glaucoma and uncontrolled IOP despite the use of maximum tolerated glaucoma medication.
  • Patients over 18 years old.
  • Patients who can understand and sign the inform consent form.

排除标准

  • Other forms of glaucoma other than open angle glaucoma; previous psiquiatric condition ;
  • Patients who can understand and sign the inform consent form;
  • visual acuity worse than hand motion;
  • previous retina surgery with buckle implant

结局指标

主要结局

intra ocular pressure

时间窗: Monthly

次要结局

  • number of hypotensive medications(monthly)

研究者

发起方
Federal University of São Paulo
申办方类型
Other

研究点 (2)

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