NCT04215627已完成不适用
Comparison Between Invasive Hemodynamic Monitoring, Using the PiCCO Monitor, to a Non-invasive Photoplethysmography Based Device in Hemodynamic Unstable Critically Ill Patients, With Vasopressor Support
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 9
- 试验地点
- 1
- 主要终点
- Level of accordance between the BB-613PW to the PiCCO
研究概览
简要总结
The aim of this study is to compare hemodynamic monitoring using the invasive PiCCO device to the BB-613PW wireless, non-invasive PPG-based device, in critically ill patients within the ICU, suffering from hemodynamic instability and in need of vasopressor support. Data will be gathered prospectively and analysed retrospectively.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 99 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •ICU adult patients in the need of vasopressor support of more than 0.2 mcg/Kg/Min for a period longer than 3 hours
- •Patients in which PiCCO monitoring is needed
排除标准
- •Refusal of the subject
- •Technical difficulties in insertion of the PiCCO catheters
- •Significant cardiac arrhythmias
- •Significant valvular disease
- •Pregnancy
结局指标
主要结局
Level of accordance between the BB-613PW to the PiCCO
时间窗: 72 hours per individual
We will compare the level of accordance of blood pressure, heart rate, stroke volume, cardiac output, heart rate variability, and systemic vascular resistance.
次要结局
未报告次要终点
研究者
研究点 (1)
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