NCT03114579已完成不适用
Evaluation of the Measurement of Cardiac Output by the NEXFIN HD Monitor in Peroperative
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 42
- 试验地点
- 1
- 主要终点
- Overall survival defines as the time between the date of surgery and death or date of last news
研究概览
简要总结
Continuous perioperative cardiac output (DC) and blood pressure (PA) monitoring contributes to hemodynamic stability and ensures adequate perfusion pressure, resulting in a reduction in morbidity and mortality and length of hospital stay.
The monitors usually used in perioperative are either semi-invasive and difficult for calibration (oesophageal Doppler) or invasive (arterial catheter).
The Nexfin HD allows these two measurements and it is completely non-invasive, remains to validate its use in peroperative.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 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
- •Adult patients candidate for surgery under general anesthesia requiring oesophageal Doppler or arterial catheter hemodynamic monitoring.
排除标准
- •Patients with cardiac and thoracic surgery,
- •patients for whom access to the head is impossible,
- •facial trauma patients,
- •patients with aortic malformation, dilation or coarctation,
- •patients with aortic dissection,
- •patients with vascular surgery with aortic clamping,
- •patients with a tumor, stenosis or varices of the esophagus,
- •patients with severe oesophagitis,
- •patients with thoracic radiotherapy
- •patients under guardianship or curatorship or deprived of liberty.
研究组 & 干预措施
Measure of the cardiac output obtained by a reference methode
Other
干预措施: Intraoperative heart rate measurement (reference method) (Device)
Measurement of cardiac output obtained by NEXFIN HD.
Other
干预措施: NEXFIN HD (Device)
结局指标
主要结局
Overall survival defines as the time between the date of surgery and death or date of last news
时间窗: 6 months
次要结局
未报告次要终点
研究者
研究点 (1)
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