NCT02365688终止不适用
Correlation of Multiple Invasive and Non-Invasive Hemodynamic Monitored Modalities to Support Goal Directed Fluid Therapy During Open Abdominal Surgery
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 18
- 试验地点
- 2
- 主要终点
- Dynamic Hemodynamic Response to Fluid Resuscitation
研究概览
简要总结
The purpose of this study is to retrospectively evaluate the hemodynamic response to goal directed fluid therapy fluid during open abdominal surgery where goal directed fluid therapy is a standard of care after establishing a pre-incision baseline response to fluids.
详细描述
Electronic and annotated observation data to support an algorithm library
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
- •Adults ≥18 years booked for an open abdominal procedure
- •American Society of Anaesthesiologists (ASA) Physical Status 1 - 3
- •Expected duration of surgical procedure to be ≥ 2 hours
- •Standard of care monitoring to include cardiac output
排除标准
- •Open chest surgical procedure expected
- •Cardiac arrhythmia such as atrial fibrillation.
- •Right Ventricular Failure
- •Aortic regurgitation
研究组 & 干预措施
Initial bolus pre-incision
Other
Initial pre-incision bolus of 500 cc of fluids with hemodynamic response recorded
干预措施: Initial bolus pre-incision (Procedure)
结局指标
主要结局
Dynamic Hemodynamic Response to Fluid Resuscitation
时间窗: Up to 6 hours but not to exceed duration of surgical procedure
Physiological parameters compared before and after fluid bolus for fluid resuscitation.
次要结局
未报告次要终点
研究者
研究点 (2)
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