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临床试验/CTRI/2023/01/049033
CTRI/2023/01/049033
尚未招募
未知

Evaluation of an automated system for glaucoma screening that runs offline on a smartphone-based fundus camera

V Prasad Eye Institute0 个研究点目标入组 0 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Health Condition 1: H401- Open-angle glaucoma
发起方
V Prasad Eye Institute
状态
尚未招募
最后更新
3年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
3年前
研究类型
Observational

研究者

发起方
V Prasad Eye Institute

入排标准

入选标准

  • 1\.Participants who can provide a written informed consent

排除标准

  • 1\.Subject with unreliable visual fields (Defined as \>20% rate of fixation losses and \>15% false\-positive and false\-negative results.)
  • 2\.Subject with SD\-OCT signal strength \< 7
  • 3\.Subject deemed to have narrow angles on gonioscopy and cannot be dilated without a laser iridotomy (PI)
  • 4\.Participants unwilling to sign the informed consent
  • 5\.Subject with acute or sudden vision loss
  • 6\.Other causes of optic neuropathy
  • 7\.Co\-existing retinal/disc pathologies that does not allow reliable assessment of disc like vitreous hemorrhage, congenital disc abnormalities, advanced retinopathy of prematurity etc
  • 8\.Significant media opacity precluding adequate view of the disc like advanced cataract as described below, corneal scars
  • 9\.Participant has a condition that, in the opinion of the investigator, would preclude participation in the study (e.g., uncontrolled intraocular pressure, active eye infection, \<3months post glaucoma filtering surgery, unstable medical status including blood pressure or glycemic control etc).
  • 10\.Participant is hypersensitive to light, known to have seizures, consuming medication that causes photosensitivity.

结局指标

主要结局

未指定

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