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
| Type | Name | Description |
|---|---|---|
| DEVICE | Ultrasonic 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.