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Clinical Trials/NCT00853437
NCT00853437
Completed
Not Applicable

Comparison of Techniques for Assessing Cardiac Output and Preload in Critically Ill Pediatric Patients

Transonic Systems Inc.1 site in 1 country7 target enrollmentJanuary 2009
ConditionsCardiac Output

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Output
Sponsor
Transonic Systems Inc.
Enrollment
7
Locations
1
Primary Endpoint
Compare CO measured by the new method with clinician's estimate and implied CO from measurement of arteriovenous oxygen content difference.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The ability to measure cardiac output (CO) accurately and reproducibly at frequent intervals remains elusive to the clinician caring for critically ill pediatric patients even though a large proportion of these children are known to have hemodynamic compromise as a result of their illness. Current techniques used in adults to measure CO are not suitable for routine use with pediatric patients. A new ultrasound dilution approach provides an opportunity to measure cardiac output and blood volumes in pediatric patients. The main aim of this study is to compare CO measured by the new method with the clinician's estimate and implied CO from the measurement of the arteriovenous oxygen content difference.

Registry
clinicaltrials.gov
Start Date
January 2009
End Date
May 2011
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with in situ central venous and arterial catheters
  • Ability to draw blood from arterial and central venous catheters
  • Presence of parent or guardian to provide consent

Exclusion Criteria

  • Patients over 16 years of age.

Outcomes

Primary Outcomes

Compare CO measured by the new method with clinician's estimate and implied CO from measurement of arteriovenous oxygen content difference.

Time Frame: 5-8 minutes minimum

Secondary Outcomes

  • Measure blood volumes to compare effects of volume infusion and furosemide.(5-8 minutes minimum)

Study Sites (1)

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