NCT06204848已完成不适用
Acquisition of Imaging Data of Vitreous Opacities in Human Eyes Using a Non-Invasive Imaging Device
PulseMedica2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年11月12日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 44
- 试验地点
- 2
- 主要终点
- Successful capture of SLO and OCT imaging data of SVOs for algorithm development
研究概览
简要总结
The goal of this clinical trial is to capture imaging data of eye floaters in the population to build an imaging database to learn more about them in. Participants will imaged with an investigational ophthalmic imaging device to capture images of their floaters.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Aged 18 years or older
- •Symptomatic vitreous opacities (floaters) in vision
- •Clear ocular media, to allow a clear view of the vitreous for the SVO-ID
排除标准
- •Younger than 18 years of age
- •Presence of vitreous hemorrhage
- •Cataract Grade 3 and above
- •Opacification of lens, cornea, or vitreous
- •Diagnosis of narrow angle glaucoma
- •Refractive error is outside the range of -6D to+3D
- •Astigmatism is outside the range of +/-2D of cylinder
结局指标
主要结局
Successful capture of SLO and OCT imaging data of SVOs for algorithm development
时间窗: Through study completion, an average of 6-8 months
Successful collection of SLO and OCT imaging data
次要结局
- Collection of patient-reported symptoms(Through study completion, an average of 6-8 months)
研究者
研究点 (2)
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