Clinical Trials Directory

Trials / Completed

CompletedNCT00883857

Comparison Endotracheal Cardiac Output Monitor (ECOM) to a Standard Device in Measuring Heart Blood Volume

Status
Completed
Phase
Study type
Observational
Enrollment
49 (actual)
Sponsor
University of California, Los Angeles · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate a new monitor that measures cardiac output (amount of blood pumped by the heart). The system that is being tested in this study, called Endotracheal Cardiac Output Monitor (ECOM), uses electricity (impedance cardiography) to measure cardiac output and is not harmful to the patient. This study will test the accuracy and efficacy of the ECOM system in anesthetized and sedated patients who, in the normal course of clinical care in the OR or ICU, are having cardiac output measured. The investigators propose that unlike the standard system for cardiac output measurement, the ConMed ECOM System should result in a simplified, inexpensive, continuous, less-invasive, and accurate method of measuring cardiac output. Such a technique could allow the rapid diagnosis of instability in the cardiovascular system for critically ill patients.

Conditions

Timeline

Start date
2007-10-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2009-04-20
Last updated
2018-06-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00883857. Inclusion in this directory is not an endorsement.