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Estimation of Cardiac Output in Neonatal ICU Using an Ultrasound Dilution Technique

Estimation of Cardiac Output in Neonatal ICU Using an Ultrasound Dilution Technique

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01610622
Acronym
CH
Enrollment
7
Registered
2012-06-04
Start date
2012-03-31
Completion date
2013-05-31
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

Neonatal Intensive Care

Keywords

Cardiac Output, Blood volumes, Neonates

Brief summary

Presently there is no apparatus, clinically available, for routine determination of cardiac output (CO) in children. The goal of this research is to develop new technology that will help determine CO in neonates.

Interventions

DEVICECOstatus cardiac output measurement with isotonic saline

Isotonic saline, which is the indicator, is injected to obtain COstatus cardiac output measurements. No other interventions are made for the purpose of the study.

Sponsors

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

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 1 Months
Healthy volunteers
No

Inclusion criteria

* All neonatal patients cared for in our ICU with umbilical venous and arterial catheters simultaneously in place for their care, will be eligible.

Exclusion criteria

* Patients would be excluded if the family/guardian denied permission or if the attending physician felt the patient was not stable.

Countries

United States

Outcome results

None listed

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