跳至主要内容
临床试验/CTRI/2021/05/033408
CTRI/2021/05/033408招募中未知

Diagnostic ability of Elisar ZEST algorithm for glaucoma in chennai main hospital

Elisar Life Sciences pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Inclusion into the control group:
  • Normal subjects will be recruited who has:
  • 1.Intraocular pressure (IOP) in AT < 21 mmHg,
  • 2.Optic disc examination graded as normal.
  • 3.No family history of glaucoma.
  • Inclusion into glaucoma group:
  • 1.Glaucoma diagnosis will be based on the presence of typical glaucomatous optic disc damage (i. e. Cup: disc ratio > 0.6, localized rim loss, optic disc hemorrhage, or cup-to-disc asymmetry > 0.2),
  • 2.IOP in AT > 21 mmHg.
  • 3.Glaucoma of any type without any secondary complications.
  • 4.Glaucomatous Optic Neuropathy (GON) detection by glaucoma expert.

排除标准

  • 1.Subjects who have undergone ocular surgeries, with ocular disease, amblyopia, neurological disorders will be excluded from the study.
  • 2.Subjects will be excluded with systemic or ocular disease other than glaucoma that might interfere with visual field results.
  • 3.The cataract greater than moderate lens opacification will be excluded from the study as per the LOCS III grading system.
  • 4.Using a miotic drug will be excluded from the study

研究者

发起方
Elisar Life Sciences pvt Ltd

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