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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 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
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

  • 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.

研究者

发起方
V Prasad Eye Institute

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