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Clinical Trials/NCT01103908
NCT01103908
Terminated
Not Applicable

Ultrasound Dilution Cardiac Output at the Conclusion of Cardiopulmonary Bypass in Pediatric Patients

Transonic Systems Inc.1 site in 1 country3 target enrollmentApril 2010
ConditionsCardiac Output

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Output
Sponsor
Transonic Systems Inc.
Enrollment
3
Locations
1
Primary Endpoint
Cardiac output after cardiopulmonary bypass
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

Cardiac output, the amount of blood pumped by the heart in one minute, will be measured in pediatric patients undergoing surgery involving cardiopulmonary bypass (CPB). Cardiac output will be measured after cardiopulmonary bypass using a device that employs ultrasound dilution technology. At times, cardiac output will be measured during a procedure called modified ultrafiltration (MUF). The ultrasound dilution cardiac output measurements will be validated or compared with cardiac output measurements made using other FDA approved techniques and devices.

Registry
clinicaltrials.gov
Start Date
April 2010
End Date
August 2011
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pediatric patients (age \< 21 years)
  • Pediatric patients undergoing surgery involving cardiopulmonary bypass

Exclusion Criteria

  • Patients aged \> 21 years
  • Patients undergoing surgery "off pump" (not involving cardiopulmonary bypass)

Outcomes

Primary Outcomes

Cardiac output after cardiopulmonary bypass

Time Frame: Less than 10 minutes

Cardiac output will be measured in pediatric patients after undergoing surgery involving cardiopulmonary bypass

Study Sites (1)

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