NCT01468103Unknown不适用
Laser Peripheral Iridotomy Versus Surgical Peripheral Iridectomy in Early Angle Closure:a Randomized Clinical Trial
Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2009年8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
- 120
- 试验地点
- 1
- 主要终点
- intraocular pressure
研究概览
简要总结
This is a randomized controlled clinical trial to compare laser peripheral iridotomy(LPI) and surgical peripheral iridectomy. Subjects of primary angle closure suspect, primary angle closure will be randomized to undergo LPI or SPI. Subjects are proposed to be followed up for 3 years.
详细描述
The following will be studied:
- To evaluate the safety of these two techniques for the treatment of angle closure.
- To compare the anterior chamber reaction and IOP changes post surgery.
- TO establish the UBM/ASOCT chamber angle parameters changes pre and post surgery.
- To assess the development of PAS.
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
- 50 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •more than 50 years old
- •Diagnosis of either: Primary angle closure suspects, Primary angle closure in need of laser iridotomy or surgical iridectomy
- •Able to give Informed concent
排除标准
- •Ophthalmic diseases other than glaucoma and cataract
- •pseudophakic or aphakic patients
- •inability to attend regular follow-up assessment or to give informed written consent
- •Secondary causes of angle closure e.g. subluxed lens, uveitis, trauma and neovascular glaucoma
- •Participating in another study
- •monocular patients
结局指标
主要结局
intraocular pressure
时间窗: 3 years
次要结局
- Angle assessment parameters(3 years)
研究者
Gao Xinbo
student
Sun Yat-sen University
研究点 (1)
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