NCT05615896终止不适用
Data Collection With the P200TE and P200TxE in Diseased Eyes for Clinical Developments
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- Optos, PLC
- 入组人数
- 5
- 试验地点
- 1
- 主要终点
- Collection of images
研究概览
简要总结
The primary objective is to collect OCT scans on a modified P200TxE and P200TE.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female volunteers 22 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed;
- •Volunteers who can follow the instructions by the clinical staff at the clinical site;
- •Volunteers who agree to participate;
- •Volunteers who have been diagnosed with retina pathology with intra-retinal and/or subretinal fluid present in the posterior pole region.
排除标准
- •Volunteers unable to tolerate ophthalmic imaging;
- •Volunteers with ocular media not sufficiently clear to obtain acceptable OCT images.
研究组 & 干预措施
P200TE Device First
Experimental
干预措施: Imaging Session (Device)
P200TxE Device First
Experimental
干预措施: Imaging Session (Device)
结局指标
主要结局
Collection of images
时间窗: 1 year
The primary endpoint will be the collection of OCT scans on the P200TE and P200TxE devices. The scans will be used by R\&D for development of a de-noising algorithm as well as other possible developments.
次要结局
未报告次要终点
研究者
研究点 (1)
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