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Impedance Cardiography: Clinical Evaluation of Endotracheal Cardiac Output Monitor (ECOM)

NCT00924482 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 261

Last updated 2023-11-28

Study results available
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Summary

1. Compare measurements of cardiac output derived from electrical measurements from electrodes on an endotracheal tube (ECOM or Endotracheal Cardiac Output Monitor) to those made from a pulmonary artery thermodilution catheter.
2. Establish the safety and efficacy of the ECOM system.

Conditions

  • Cardiac Output

Interventions

DEVICE

Placed ECOM endotracheal cardiac output monitor in patients undergoing cardiac surgery

Measure cardiac output during perioperative period and compare to pulmonary artery thermodilution cardiac output measurements.

Sponsors & Collaborators

Principal Investigators

  • Art Wallace, MD, PhD · University of California, San Francisco

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-01-31
Primary Completion
2008-09-30
Completion
2008-09-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00924482 on ClinicalTrials.gov