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临床试验/TCTR20230706008
TCTR20230706008已完成不适用

Effect of Blue Light-Filtered Intraocular Lens on Contrast Sensitivity of Glaucoma Patients

Faculty of Medicine Siriraj Hospital0 个研究点目标入组 42 人开始时间: 2023年7月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
42

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

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • Subjects must be at least 18 years of age.
  • Subjects must be a good controlled definite glaucoma patient (Definite: glaucomatous visual field defect and possible glaucomatous optic neuropathy [vertical cup-to-disc ratio more than 0.7 or asymmetry between eyes more than 0.2 or minimum rim width less than 0.1] Rotterdam study criteria)
  • Subjects must have significant cataract (BCVA less than 6/18) with no previous cataract surgery.
  • Subjects must be able to communicate in Thai or English, understand risk and benefits of this study, able to make follow-up visits, and voluntarily join the study.

排除标准

  • Subjects who fails to cooperate in the measurement of contrast sensitivity.
  • Subjects who have pathology of cornea, vitreous body, retina, or optic nerve that would adversely affect visual performance.
  • Patients with other active ocular diseases.

研究者

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