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OpenTrials
Completed

NCT Number: NCT01610622

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

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.

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Key information

Age range

Up to 1 month

Sex eligibility

All sexes

Study type

Observational

Primary location

Crouse Hospital

Syracuse, New York, 13210, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

COstatus cardiac output measurement with isotonic saline

Device

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 and collaborators

Lead sponsor

Transonic Systems Inc.

Industry

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Acronym: CH

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jun 4, 2012
Registry last updated
May 27, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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