Anonymized Data Collection From the CardiacSense1 and Other Modalities for the Purpose of Developing a System for Monitoring of Respiratory Rate
试验速览
- 阶段
- 不适用
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Respiratory rate
研究概览
简要总结
Collect data from the CardiacSense1's sensors and Capnograph, for the purpose of developing a wearable system for monitoring of Respiratory Rate (RR) in patients while at hospital
详细描述
Hospitalized subjects, diagnosed with a Respiratory disease or subjects with no known Respiratory disease will be will be connected simultaneously to CardiacSense watch and Capnograph for a duration of at least 30 minutes and up to 24 hours in order to collect data for the purpose of developing a wearable system for monitoring of Respiratory Rate (RR) by the CardiacSense watch.
The CardiacSense1 is a wrist worn device designed to detect atrial fibrillation. CardiacSense1 senses the radial artery inflation and deflation and together with a PPG sensors give an ultimate performance that is superior to PPG only.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 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
- 否
入选标准
- •Age of eighteen (18) year and above
- •Diagnosed with Respiratory disease/impairment or without any known Respiratory disease/impairment
- •Ability and willingness to sign an informed consent form
排除标准
- •Subjects who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the subject's participation in this study
- •Patients with significant co morbidities (assessed by the clinician at screening only
- •Presence of an acute disease process that might interfere with test performance
- •Subjects with PPG SNR <100 indicated by the CardiacSense1 device
- •Women who are pregnant or breastfeeding
结局指标
主要结局
Respiratory rate
时间窗: 24 hours
Capnograph and Cardiacsense1 sensor Respiratory rate
次要结局
未报告次要终点