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临床试验/NCT01774227
NCT01774227已完成不适用

A Randomized Trial of the Pops-titration Versus the Slow-coagulation Energy Delivery Technique on the Outcome of Diode Laser Transcleral Cyclophotocoagulation in Treatment of Neovascular Glaucoma With Dark Iris

Prince of Songkla University1 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2013年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
98
试验地点
1
主要终点
Success rate

研究概览

简要总结

  • Transcleral cyclophotocoagulation (TSCPC) has long been used as refractory glaucoma management and is very easy to learn and easy to perform.
  • Recent advances in laser technology; the role of TSCPC is being expanded because it has benefits of noninvasive glaucoma procedure.
  • The titration (pops), the fixed high-energy, and the fixed-low energy (slow-coagulation) are three energy delivery techniques.
  • The present study would report on the outcome (efficacy and safety) of the slow-coagulation versus the titration method in treatment of refractory glaucoma with dark iris.
  • The results would provide reliable evidences to supplement clinical judgment when making a decision in favor of each treatment method for glaucoma patients.

详细描述

  • Several protocols afford delivery of the "optimum" dose of laser energy per session necessary to achieve a long-term effective ocular hypotensive response balancing risks related to a high energy treatment and risks related to retreatment due to suboptimum dose delivery.
  • There are two main approaches to delivering laser energy, the pops-titration method and the fixed energy method that are the fixed-high and low-energy (the Gaasterland's slow-coagulation technique).
  • Of particular interest is which laser energy delivery method (slow-coagulation versus pops-titration) affords the optimal dose of photocoagulation necessary to achieve an effective long-term intraocular pressure (IOP) reduction while minimizing the risk of adverse events related to overtreatment and retreatments especially in refractory glaucomatous eyes with dark iris color.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Refractory glaucoma (Neovascular glaucoma) with
  • •Eyes with no visual potential and very high intraocular pressure (on maximal medical treatment) in which the intraocular pressure will probably cause corneal complications
  • •Eyes with no visual potential and very high intraocular pressure (on maximal medical treatment) in which the intraocular pressure cause eye pain and need pain relief
  • •Eyes with minimal useful vision and intraocular pressure over the target intraocular pressure
  • •Eyes in which trabeculectomy with mitomycin-C and/or drainage implants have a high probability of failure
  • •Eyes in which trabeculectomy with mitomycin-C and/or drainage implants have previously failed
  • •Patient refuses to undergo more aggressive intraocular surgery
  • •Patients whose general medical condition precludes invasive surgery

排除标准

  • •The visual acuity in the fellow eye is no light perception
  • •Have previously been treated by the transcleral cyclophotocoagulation
  • •Allergy to anesthetic medication
  • •Can not measure the intraocular pressure by the applanation method

研究组 & 干预措施

The pops-titration group

Experimental

The titration method uses power that is titrated according to the audible "pop".

干预措施: The pops-titration group (Procedure)

The slow-coagulation group

Experimental

The slow-coagulation group utilize the low-energy using the Gaasterland's slow-coagulation technique

干预措施: The slow-coagulation group (Procedure)

结局指标

主要结局

Success rate

时间窗: 60 months

Success rate defined as the proportion of eyes achieving an intraocular pressure between 6 and 21mmHg with or without topical antiglaucoma medication at the final follow up visit.

次要结局

  • Response rate(60 months)
  • Cyclodiode efficacy index(60 months)
  • Failure rate(60 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Weerawat Kiddee

Dr.Weerawat Kiddee

Prince of Songkla University

研究点 (1)

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