RecruitingACTRN12608000486325

A randomised controlled trial of non-invasive cardiac output monitoring in the emergency room:

A randomised controlled trial of non-invasive cardiac output monitoring on oxygen delivery in critically ill emergency department patients.


Sponsor

Ogilvie Thom

Enrollment

222 participants

Start Date

Nov 1, 2008

Study Type

Interventional

Conditions

Summary

Critically ill patients often have signs of inadequate oxygen delivery. We know this adversely impacts on survival. The hypothesis is that the introduction of non invasive cardiac output monitoring will allow us to improve or correct oxygen delivery, thus possibly improving survival


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria1

  • Critically ill adults in the ED requiring referral to Intensive Care for consideration of admission.

Exclusion Criteria1

  • Age < 18

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Interventions

Subjects will be allocated to standard care plus non-invasive cardiac output monitoring (intervention). Non-invasive cardiac output monitoring for four hours in the Emergency Department (ED).

Subjects will be allocated to standard care plus non-invasive cardiac output monitoring (intervention). Non-invasive cardiac output monitoring for four hours in the Emergency Department (ED).


Locations(1)

Australia

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ACTRN12608000486325