NCT01083147已完成不适用
Age-Related Macular Degeneration (AMD) - Beta Study Telemedicine Assessment
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Subject compliance with Foresee HomeTM device
研究概览
简要总结
The purpose of this study is to evaluate the compliance of the Foresee Home device in intermediate AMD patients.
详细描述
This is a non-randomized cohort, multi-center study. The eligible subjects will be asked to use the FORESEE HOME device daily and the tests results will be automatically transmitted to the Data Monitor Center for analysis.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 50 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects who successfully completed participation in ForeseeHome-US2 study
- •Patients with ability to comprehend and sign the informed consent/authorization
排除标准
- •Subjects who failed to complete participation in ForeseeHome-US2 study
结局指标
主要结局
Subject compliance with Foresee HomeTM device
时间窗: 6 months
次要结局
- Assessment of the Telemedicine infrastructure(6 months)
研究者
研究点 (1)
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