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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00853437
Acronym
GCH
Enrollment
7
Registered
2009-03-02
Start date
2009-01-31
Completion date
2011-05-31
Last updated
2016-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Output

Keywords

Comparison of CO by new method to clinician's estimate and implied CO from the measurement of arteriovenous oxygen content difference.

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.

Interventions

None listed

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Transonic Systems Inc.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 16 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Compare CO measured by the new method with clinician's estimate and implied CO from measurement of arteriovenous oxygen content difference.5-8 minutes minimum

Secondary

MeasureTime frame
Measure blood volumes to compare effects of volume infusion and furosemide.5-8 minutes minimum

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026