Clinical Trials Directory

Trials / Completed

CompletedNCT01460329

Comparing Cardiac Output Measurements in Critically Ill Children Using USCOM and Transthoracic ECHO

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

Status
Completed
Phase
Study type
Observational
Enrollment
22 (actual)
Sponsor
University of North Carolina, Chapel Hill · Academic / Other
Sex
All
Age
1 Day – 17 Years
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DEVICEUltrasonic Cardiac Output Monitor (USCOM).This device is FDA approved and based on the principles of ECHO using continuous-wave Doppler ultrasound to measure cardiac output.

Timeline

Start date
2011-10-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2011-10-26
Last updated
2013-05-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01460329. Inclusion in this directory is not an endorsement.

Comparing Cardiac Output Measurements in Critically Ill Children Using USCOM and Transthoracic ECHO (NCT01460329) · Clinical Trials Directory