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临床试验/NCT04764734
NCT04764734进行中(未招募)不适用

A Validation Study of the NightOwl Home Sleep Apnea Test

Ectosense NV8 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年3月20日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
100
试验地点
8
主要终点
The Evaluation of the Level of Agreement (Classification Accuracy) Between Patient Categorization

研究概览

简要总结

The objective of this study is to evaluate the performance of a miniaturized sleep apnea test, called NightOwl. The system consists of a sensor placed on the fingertip and a cloud-based analytics software. The sensor acquires accelerometer and photoplethysmographic data. The software derives actigraphy from the former, and blood oxygen saturation and peripheral arterial tone (PAT), among other features, from the latter. In order to assess NightOwl's performance, the investigators will compare the apnea hypopnea index (AHI) estimate, defined as the number of respiratory events per hour of sleep, derived by the NightOwl system, to the apnea-hypopnea index (AHI) obtained from manual analysis of the polysomnography (PSG), which is the gold standard for sleep apnea diagnosis. This study will be performed in a sleep lab environment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
13 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with an indication for an in-lab polysomnography

排除标准

  • Intellectually disabled people

结局指标

主要结局

The Evaluation of the Level of Agreement (Classification Accuracy) Between Patient Categorization

时间窗: Through study completion, an average of 1 month.

The evaluation of the level agreement (classification accuracy) between patient categorization (into sleep apnea severity categories) obtained by the NightOwl and those obtained by the PSG. This measure is calculated by dividing the number of participants on which both NightOwl and the PSG agree on the sleep apnea severity category by the total number of participants.

次要结局

未报告次要终点

研究者

发起方
Ectosense NV
申办方类型
Industry
责任方
Sponsor

研究点 (8)

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