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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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
UCLA
Los Angeles, California, United States
Start Date
October 1, 2007
Primary Completion Date
November 1, 2010
Completion Date
November 1, 2010
Last Updated
June 12, 2018
49
ACTUAL participants
Lead Sponsor
University of California, Los Angeles
NCT06690151
NCT05647213
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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