Cardiac Output Monitoring in Critically Ill Patient Undergoing Intubation
| Status: | Recruiting |
|---|---|
| Conditions: | Cardiology, Hospital |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Other |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 8/10/2018 |
| Start Date: | June 27, 2018 |
| End Date: | December 15, 2019 |
| Contact: | Anita Stoltenberg, RRT |
| Email: | Stoltenberg.Anita@mayo.edu |
| Phone: | 507-285-7157 |
Non-invasive Cardiac Output Monitoring (NICOM) in Critically Ill Patient Undergoing Endotracheal Intubation in ICU
Collect hemodynamic data, such as heart rate, blood pressure, and cardiac output to help
understand the effect of pre and post intubation.
understand the effect of pre and post intubation.
A Non-invasive physiologic monitor, Non-Invasive Cardiac Output Monitor (NICOM), will be
utilized for this study. This is the first completely non-invasive hemodynamic device
approved by the FDA and available for clinical use produced by Cheetah Medical and utilizes
Bioreactance (Tel Aviv, Israel). It performs accurately and with precision in all patient's
studied and requires only 4 adhesive gel pads on the skin to measure continuous cardiac
output and to calculate Stroke Volume Variation (SVV). Other physiologic data (blood
pressure, total peripheral resistance (TPR), stroke volume (SV), and heart rate) will be
analyzed in real time and recorded on the device and downloaded into an excel database. The
data on the device will be downloaded weekly onto the excel database and deleted on the
device. The Study personnel will be trained in its use prior to study initiation.
utilized for this study. This is the first completely non-invasive hemodynamic device
approved by the FDA and available for clinical use produced by Cheetah Medical and utilizes
Bioreactance (Tel Aviv, Israel). It performs accurately and with precision in all patient's
studied and requires only 4 adhesive gel pads on the skin to measure continuous cardiac
output and to calculate Stroke Volume Variation (SVV). Other physiologic data (blood
pressure, total peripheral resistance (TPR), stroke volume (SV), and heart rate) will be
analyzed in real time and recorded on the device and downloaded into an excel database. The
data on the device will be downloaded weekly onto the excel database and deleted on the
device. The Study personnel will be trained in its use prior to study initiation.
Inclusion Criteria:
- Patients requiring endotracheal intubation in the intensive care unit.
Exclusion Criteria:
- Patients previously enrolled in this study.
- Patients requiring intubation outside of the intensive care unit.
We found this trial at
2
sites
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Rochester, Minnesota 55905
Principal Investigator: Nathan Smischney, MD
Phone: 507-285-7157
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