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NCT00883857 Clinical Trial

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

Cardiac Surgery Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00883857
Other study ID # 06-04-090-03
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2007
Est. completion date November 2010

Study information
Verified date June 2018
Source University of California, Los Angeles
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 49
Est. completion date November 2010
Est. primary completion date November 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Able to give informed consent

- Patients requiring all of the following:

- an oral ET tube

- an arterial catheter

- measurement of CO

Exclusion Criteria:

- Patients not competent to give informed consent

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States UCLA Los Angeles California

Sponsors (1)
Lead Sponsor Collaborator
University of California, Los Angeles

Country where clinical trial is conducted

United States, 

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