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临床试验/NCT02945748
NCT02945748已完成不适用

Uninvasive Cardiac Output Monitoring (USCOM) in Critically Ill Children: Validation and Prediction of Hemodynamic Instability

Rabin Medical Center1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2016年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
52
试验地点
1
主要终点
Raise>10% in cardiac index following therapy

研究概览

简要总结

Hemodynamically unstable ventilated PICU & PCICU patients, which a decision for commencement in inotropic therapy or fluid bolus has been made, will be recruited. Hemodynamic measurements will be carried out before and after therapy have been made, including customary hemodynamic parameters, echocardiography and USCOM studies.

All parameters will be analyzed for fluid responsiveness or inotropic therapy prediction. Trend in USCOM parameters will be compared to echocardiography CO parameters.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
2 Days 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Pediatric critically ill ventilated patients admitted to PICU & PCICU
  • Hemodynamically unstable which a decision for commencement in inotropic therapy or fluid bolus has been made
  • parental concent

排除标准

  • Cardiac shunt
  • Aortal anomaly \ Repair
  • Tracheostomy
  • Parental refusal to participate

结局指标

主要结局

Raise>10% in cardiac index following therapy

时间窗: 20 minutes

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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