NCT03482505终止不适用
Rainbow Acoustic Monitoring (RAM) in Patients Weighing up to 10kg Comparison Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 10
- 试验地点
- 4
- 主要终点
- Accuracy of Acoustic Respiration Rate (RRa)
研究概览
简要总结
The objective of this clinical investigational study is to compare the acoustic respiration rates (RRa) obtained using the INVSENSOR0004 sensor in the subjects up to 10 kg with the respiration rates determined by manual annotations (RRref), and when applicable with capnography respiration rate (RRcap).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects weighing up to 10kg
- •Subjects will be inpatients and/or outpatients admitted to the NICU (Neonatal Intensive Care Unit) or PICU (Pediatric Intensive Care Unit) or PACU (Post-Anaesthesia Care Unit)
- •The parent/legal guardian has given written informed consent/assent to participate in the study.
排除标准
- •Subjects with underdeveloped skin
- •Subjects with skin abnormalities at the planned application sites that may interfere with sensor application, per directions-for-use (DFU) or trans-illumination of the site, such as burns, scar tissue, infections, abnormalities, etc.
- •Subjects deemed not suitable for the study at the discretion of the investigator.
结局指标
主要结局
Accuracy of Acoustic Respiration Rate (RRa)
时间窗: One study visit lasting up to 60 minutes.
Acoustic respiration rate (RRa) as determined by the INVSENSOR00004 will be compared to measurements of actual respiration rates as determined by manual annotation of recorded respiration waveform (RRref) data. Evaluation of the RRa measurements will be reported as bias between the RRa and the RRref.
次要结局
未报告次要终点
研究者
研究点 (4)
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