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临床试验/CTRI/2014/05/004639
CTRI/2014/05/004639已完成未知

Glaucoma treatment by cyclo-coagulation using High Intensity Focused Ultrasound (EyeOP medical device system) in Indian Patients

EyeTechCare0 个研究点目标入组 15 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
15

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

入选标准

  • 1.Primary Open Angle or Angle Closure Glaucoma and Secondary Glaucoma
  • 2.Patient with no vision potential or blind eyes
  • 3.No previous intraocular surgery or laser treatment during the 90 days before HIFU Day
  • 4.Any patient with/without previous conventional glaucoma surgery failure
  • 5.Angle closure glaucoma or narrow anatomical anterior chamber as identified by gonioscopy and classified as Shaffer Grade 0 or 1
  • 6. Any patient with/without previous conventional glaucoma surgery failure

排除标准

  • 1. Patient who has been diagnosed for normal tension glaucoma
  • 2. Glaucoma drainage device implanted and still presented in the eye to be treated
  • 3. Ocular or retrobulbar tumor
  • 4. Ocular infection within 14 days prior to the HIFU procedure
  • 5. Ocular disease other than glaucoma that may affect assessment of visual acuity and/or IOP

研究者

发起方
EyeTechCare

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