NCT04765878Unknown不适用
RespirAq Humidification During Post-operative Invasive Mechanical Ventilation in Scheduled Cardiothoracic Surgical Patients: a Feasibility Study
适应症
试验速览
- 阶段
- 不适用
- 入组人数
- 20
- 主要终点
- Humidity
研究概览
简要总结
This study aims to capture preliminary safety and effectiveness information on a near-final humidifier device design and to provide data for more extensive research, if required. This feasibility study will investigate the following: process, resources, management, and scientific aspects of delivering humidification by the RespirAq humidifier device in ventilated patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 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
- •Patients scheduled for coronary artery bypass surgery (CABG) will be recruited before their surgical procedure at the Waikato district health board during February, March, and April of 2021.
排除标准
- •Age <18 years
- •Have any other condition which, at the investigator's discretion, is believed may present a safety risk or impact the feasibility of the study or the study results
- •Patients admitted for emergency CABG surgery
- •Unable to provide written informed consent before surgery
- •Patients who would be contra-indicated to HME humidification devices
结局指标
主要结局
Humidity
时间窗: max 24 hours
Meet ISO standard
Temperature
时间窗: max 24 hours
Meet ISO standard
次要结局
未报告次要终点
研究者
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