ACTRN12612000770864已完成未知
A comparison of a new, non-invasive device for the estimation of stroke volume with the continuous thermodilution technique using a pulmonary artery catheter, before and after a fluid bolus in patients undergoing cardiac surgery.
Dr. Alan J. Broderick0 个研究点目标入组 25 人开始时间: 2012年7月19日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 25
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Diagnosis
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •Patients due to undergo cardiac surgery.
- •Pulmonary artery catheter required to be inserted prior to commencement of surgery.
排除标准
- •Patient refusal (or inability to provide full informed consent).
- •Ejection fraction <30% (avoids potential difficulties with giving the fluid bolus).
- •Cardiac arrhythmias present at induction.
- •Known moderate (or worse) tricuspid regurgitation (makes thermodilution estimates of CO inaccurate).
- •Known moderate (or worse) aortic regurgitation (previous studies using pulse contour analysis have excluded these – causes an abnormal pulse signal).
- •Presence of an intra-aortic balloon counterpulsation device (cause an abnormal pulse signal, device may give inaccurate readings).
- •Known haemoglobinopathy (novel device will not read correctly).
研究者
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