跳至主要内容
临床试验/NCT00695747
NCT00695747已完成不适用

Intraocular Pressure Control Following One Site Versus Two Site Combined Phacoemulsification/IOL And Trabeculectomy

Lahey Clinic2 个研究点 分布在 1 个国家目标入组 95 人开始时间: 1998年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Lahey Clinic
入组人数
95
试验地点
2
主要终点
Post-Op outcomes of IOP less than or equal to 16mm Hg without additional ocular hypotensive medications

研究概览

简要总结

The purpose of this study is to compare the safety & effectiveness of the two types of cataract and glaucoma surgeries. Results from this study may improve the surgical and post surgical management and long term management of patients with these conditions in the future

详细描述

The purpose of this study is to determine whether a Two-Site Technique for the Combined Procedure for subjects with coexisting visually significant glaucoma & cataracts will result in an improvement in IOP control in both the immediate and longer term postoperative period as compared with the currently Standard One Site surgical technique for both glaucoma and cataracts.

Research and data indicate that the success rate of the glaucoma part of this operation may be improved if the incision for the cataract part of the operation is separated from the drainage hole created for the glaucoma part, the constant drainage through this hole is what lowers the intraocular pressure after surgery. Using the Two-Site Combined procedure the glaucoma incision(drainage hole) will still be created superiorly, under the upper lid. The cataract incision will be moved to the temporal side of the eye ball, away from the drainage hole for the glaucoma.

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

性别
All
接受健康志愿者

入选标准

  • Meet the current criteria for combined procedure surgery:
  • A visually significant cataract(ie: an opacification of the crystalline lens resulting in a reduction of visual performance affecting daily living
  • Open angle or mixed mechanism glaucoma inadequately controlled on current therapy, or requiring two or more medications for control, or with advanced visual field and optic nerve damage.

排除标准

  • Subjects with normal tension glaucoma(defined as those subjects in whom no IOPs greater than 21 mm Hg[preceding or during therapy]have been recorded)
  • Subjects with uveitis
  • Subjects with neovascular glaucoma
  • Severe conjunctival inflammation or scarring
  • Subjects who have had previous incisional ocular surgery in the same eye
  • No subjects will have second eye operated on within 8 weeks of the first eye

结局指标

主要结局

Post-Op outcomes of IOP less than or equal to 16mm Hg without additional ocular hypotensive medications

时间窗: Assessments made at 3 months post op, 3 month intervals for at least 2 years post surgery

次要结局

未报告次要终点

研究者

发起方
Lahey Clinic
申办方类型
Other

研究点 (2)

Loading locations...

相似试验