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临床试验/ChiCTR-TRC-14004233
ChiCTR-TRC-14004233已完成不适用

晶體切除手術或內鏡光凝激光聯合晶體切除手術用於治理慢性原發性閉角型青光眼之研究

Department of Ophthalmology and Visual Sciences, the Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2014年2月13日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
The primary outcome measures are IOP and the number of IOP-lowering drugs.

研究概览

简要总结

晶體切除手術或內鏡光凝激光聯合晶體切除手術用於治理慢性原發性閉角型青光眼

研究设计

研究类型
干预性研究
主要目的
随机平行对照

入排标准

年龄范围
18 至 —(—)
性别
All

入选标准

  • A diagnosis of PACG;
  • Requiring 2 or more IOP-lowering drugs to control IOP, or IOP >21mmHg on maximally tolerable drugs;
  • Able and willing to give informed consent, prior to randomization;
  • Older than 18 years of age.

排除标准

  • Previous intraocular surgery or cyclophotocoagulation, with the exception of laser peripheral iridotomy and argon laser peripheral iridoplasty;
  • Secondary causes of angle closure including iridocorneal-endothelial syndrome, neovascular glaucoma etc.;
  • Unable to cooperate for reliable visual field and OCT examination.

研究组 & 干预措施

Experimental group

-Combined Phacoemulsification-Endoscopic Cyclophotocoagulation(Phaco-ECP) -Phacoemulsification, for two years

Contro group

Phaco-ECP, Phacoemulsification to remove the cataratous lens and insertion of an intraocular lens and endoscopic cyclophotocoagulation to ablate the ciliary processes to reduce aqueous production and achieve further IOP reduction.

结局指标

主要结局

The primary outcome measures are IOP and the number of IOP-lowering drugs.

次要结局

  • Secondary outcome measures include BCVA, surgical complications, and need for additional surgical interventions.

研究者

发起方
Department of Ophthalmology and Visual Sciences, the Chinese University of Hong Kong

研究点 (1)

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