Clinical Evaluation of the Automatic Oxygen Adjustment by FreeO2 in a Medical Population in Hospital
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
- % of time in the set SpO2 target
研究概览
简要总结
Evaluation of automatic titration of oxygen with a new version of FreeO2 (V4)
详细描述
In the previous studies, the investigators used many times automatic titration of oxygen on spontanous breathing patient (FreeO2 device) with a prototype develop in our lab in collaboration with Laval university. In this study, we want to evaluate the new version of the FreeO2 device (V4)
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
- 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 > or = 18 years old
- •Patient receiving oxygen between 1 to 6 lpm for medical pathology
- •Admitted to a medical service for less than 72 hours (emergency room not included)
排除标准
- •Unreliable SpO2 signal
- •Emergency or intensive care hospitalization
- •Absence of NIV or intubation criteria at baseline
- •Sleep apnea not paired
- •Long-term Oxygen Therapy
- •Active delirium and cognitive impairment preventing informed consent
研究组 & 干预措施
Automated oxygen adjustment
All patient in this study have automatic oxygen titration and automatic oxygen weanning
干预措施: FreeO2 (Device)
结局指标
主要结局
% of time in the set SpO2 target
时间窗: During 3 days of hospitalization or until Oxygen weaning
Continuous SpO2 monitoring (1 data each second) will be recorded, the % of time within the SpO2 target±2% set by the physician will be considered (Time in the target±2/Total recording time)
次要结局
- Oxygenation data(3 hospitalisations day or until Oxygen weaning)
研究者
François Lellouche
Principal Investigator
Laval University