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。
研究者
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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