跳至主要内容
临床试验/ISRCTN44464607
ISRCTN44464607已完成不适用

The effectiveness of early lens extraction with intraocular lens implantation for the treatment of primary angle closure glaucoma: a randomised controlled trial (EAGLE)

HS Grampian0 个研究点目标入组 400 人开始时间: 2008年10月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Both males and females, age >=50 years
  • 2. Diagnosis: either one of the following two types of patients: (i) primary angle-closure glaucoma (PACG), or (ii) primary angle-closure (PAC) with intraocular pressure (IOP) >30 mm Hg
  • 3. Newly diagnosed, i.e. either (i) untreated or (ii) under medical treatment for 6 months or less
  • 4. Angle closure (iridotrabecular contact) in 180 degrees or more
  • 5. Patient must be phakic in the affected eye(s)
  • 6. Written informed consent obtained

排除标准

  • 1. Advanced glaucoma in the potentially eligible eye as determined by either: (i) visual field loss (mean deviation worse than -15dB) or (ii) cup-disc-ratio >0.9
  • 2. Previously diagnosed acute angle closure attack in the potentially eligible eye
  • 3. Increased surgical risk: e.g., corneal opacity, Fuch's endothelial dystrophy, pseudoexfoliation, previous vitreo-retinal surgery, not able to be positioned to undergo standard technique
  • 4. Symptomatic cataract in either eye
  • 5. Previous cataract surgery or laser iridotomy in study eye
  • 6. Axial length <19 mm (nanophthalmos)
  • 7. Secondary angle closure glaucoma
  • 8. History of retinal ischaemia, macular oedema or wet age-related macular degeneration
  • 9. Medically unfit for surgery or for completion of the trial
  • Removed from the protocol as of 04/11/10:
  • 10. Life expectancy <3 years

研究者

发起方
HS Grampian

相似试验