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Clinical Trials/ACTRN12612000770864
ACTRN12612000770864
Completed
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 sites25 target enrollmentJuly 19, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Patients who require a pulmonary artery catheter to be inserted in order to measure cardiac output as part of their anaesthetic care when undergoing cardiac surgery.
Sponsor
Dr. Alan J. Broderick
Enrollment
25
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 19, 2012
End Date
March 16, 2016
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr. Alan J. Broderick

Eligibility Criteria

Inclusion Criteria

  • Patients due to undergo cardiac surgery.
  • Pulmonary artery catheter required to be inserted prior to commencement of surgery.

Exclusion Criteria

  • 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).

Outcomes

Primary Outcomes

Not specified

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