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

Completed

• Conditions: Neonatal Intensive Care

• Registration Number: NCT01610622
• Lead Sponsor: Transonic Systems Inc.

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-03
• Study First Submitted: 2012-05-30
• Study First Submitted QC: 2012-06-01
• Study First Posted: 2012-06-04
• Primary Completion: 2013-05
• Study Completion: 2013-05
• Status Verified: 2016-05
• Last Update Submitted: 2016-05-25
• Last Update Posted: 2016-05-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 7

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.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Crouse Hospital; 🇺🇸 Syracuse, New York, United States