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Clinical Trials/NCT00783679
NCT00783679
Withdrawn
N/A

Determining the Feasibility and Accuracy of Exhaled CO2 to Measure Cardiac Output in Ventilated Patients Without Tracheal Intubation

Massachusetts General Hospital1 site in 1 countryNovember 2009

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cardiac Physiology
Sponsor
Massachusetts General Hospital
Locations
1
Primary Endpoint
To test the feasibility and accuracy of using NICO to measure cardiac output in ventilator assisted patients without tracheal intubation.
Status
Withdrawn
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to test the accuracy of a new noninvasive way to measure how much blood our heart pumps per minute. This new way measures the heart's pumping activity from outside the body, instead of breaking the skin and measuring it from the inside.

Subjects will breathe normally through a mask while we record how fast and how much air they are breathing. We will have them "re-breathe" some of the air they breathed out by adjusting the ventilator. During this time, we will use the air breathed out to calculate how much blood per minute the subject's heart is pumping. We will also measure how much blood the heart is pumping at this time by injecting fluid into the catheter in the neck and then drawing about 1 teaspoon of blood from the catheters in the neck and arm. We will compare the calculated and measured values of the amount of blood pumped out of the heart for accuracy.

After we complete this procedure, we will remove the mask and allow you to rest for 10-30min. Following the rest period, we will repeat the process and collect a second set of measurements. We will draw a total of 4 teaspoons of blood for the study.

If you cannot comfortably breathe along with the ventilator, we will withdraw you from the study. If you want to stop taking part in the study at any time, let the study doctor know that you wish to withdraw. We will take off the mask, and your time in the study will end. This decision will not affect your regular medical care.

Registry
clinicaltrials.gov
Start Date
November 2009
End Date
December 2010
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Robert M. Kacmarek

Professor of Anesthesia, Director of Respiratory Care Services

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Patient is already monitored with a pulmonary artery catheter and arterial line (not for the purpose of this study);
  • Hemodynamic stability.

Exclusion Criteria

  • Patients with facial deformity, heavy beard or moustache which prevents good seal between the mask and the face;
  • Patients who have central nervous system disorders that might be adversely affected by CO2 rebreathing, such as head trauma patients with increased intracranial pressure;
  • Patients with severe tricuspid regurgitation;
  • Patients with intra-cardiac shunts;
  • Patients who cannot cooperate and synchronize with the ventilator;
  • Patients with unstable respiratory conditions, such as acute respiratory failure;
  • Patients who have claustrophobia and cannot wear the mask.
  • Patients with aortic stenosis.
  • Patients with left main coronary artery disease.

Outcomes

Primary Outcomes

To test the feasibility and accuracy of using NICO to measure cardiac output in ventilator assisted patients without tracheal intubation.

Time Frame: 1 year

Study Sites (1)

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