DRKS00018351已完成不适用
Validity of device-internal AHI detection during OSA therapy with regard to its application in telemonitoring - Tele-AHI
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 136
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
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Polysomnographic or polygraphic control of a device based sleep apnoea therapy with devices of the types AirSense 10 Autoset, AirSense 10 Elite, AirSense 10 Autoset for Her, SOMNObalance, SOMNOsoft 2 oder prismaSMART
排除标准
- •Mask leakage >25L/min, therapy duration during recording time <4h, if a nasal mask was used: mouth leakage time >10% of therapy duration
研究者
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