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Clinical Trials/NCT01996956
NCT01996956
Completed
Not Applicable

Prediction of Fluid Responsiveness by NICOM (Non-invasive Cardiac Output Monitoring) in Children With Congenital Heart Disease After Cardiac Surgery

Seoul National University Hospital1 site in 1 country30 target enrollmentMay 2013
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ConditionsFluid Responsiveness

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fluid Responsiveness
Sponsor
Seoul National University Hospital
Enrollment
30
Locations
1
Primary Endpoint
stroke volume index
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to evaluate the ability of fluid responsiveness by stroke volume variation value of NICOM(Noninvasive cardiac output monitor)system during congenital cardiac surgery.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
October 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jin-Tae Kim

Ph.D

Seoul National University Hospital

Eligibility Criteria

Inclusion Criteria

  • •congenital cardiac surgery
  • •\< 6 years old
  • •who were required the evaluation by transesophageal echocardiography

Exclusion Criteria

  • •right heart failure
  • •supported by more than 2 inotropic agents
  • •reduced kidney function
  • •any valvar stenosis
  • •moderate or severe tricuspid regurgitation
  • •single ventricle

Outcomes

Primary Outcomes

stroke volume index

Time Frame: before and after volume loading (20 min)

Volume loading was performed for 20 minutes. Stroke volume measured before and after volume expansion using transesophageal echocardiography. And, stroke volume variation of NICOM monitor was recorded before fluid loading.

Secondary Outcomes

  • Cardiac index(before and after fluid loading (20 min))

Study Sites (1)

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