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Clinical Trials/NCT01460329
NCT01460329
Completed
Not Applicable

Comparing Cardiac Output Measurements in Critically Ill Children Using Ultrasonic Cardiac Output Monitor and Transthoracic Echocardiography.

University of North Carolina, Chapel Hill1 site in 1 country22 target enrollmentOctober 2011
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ConditionsCritical IllnessPediatrics

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Critical Illness
Sponsor
University of North Carolina, Chapel Hill
Enrollment
22
Locations
1
Primary Endpoint
Cardiac Index
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to compare the accuracy and precision of two non-invasive methods of measuring cardiac output in critically ill children (<18 yrs). The participants will include any patient admitted to Pediatric intensive care unit (PICU) requiring a trans-thoracic ECHO (TTE) as part of their treatment plan. Measurements of intermittent cardiac output will be obtained and compared on participants using standard 2-D TTE and Ultrasound Cardiac Output Monitor (USCOM).

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
June 2012
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nina Verdino, MD

Principal Investigator

University of North Carolina, Chapel Hill

Eligibility Criteria

Inclusion Criteria

  • •Any UNC PICU patient \<18 yrs requiring a transthoracic ECHO (TTE) as standard of care.
  • •Gestational age \>36 weeks
  • •Wt \> 2 kg
  • •Written informed parental permission

Exclusion Criteria

  • •Any patient with known unrepaired intracardiac shunt lesion (ASD,PDA,VSD)
  • •any post operative patient with delayed closure of chest
  • •parental refusal to participate

Outcomes

Primary Outcomes

Cardiac Index

Time Frame: measured at the time of study

Study Sites (1)

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