Cardiac Output Monitoring in Critically Ill Patient Undergoing Intubation

Status Completed

Clinical Trial Summary

Collect hemodynamic data, such as heart rate, blood pressure, and cardiac output to help understand the effect of pre and post intubation.

Clinical Trial Description

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. ;

Study Design

Related Conditions & MeSH terms

Hypotension

Clinical Trial Details

NCT number	NCT03525743
Study type	Observational
Source	Mayo Clinic
Contact
Status	Completed
Phase
Start date	June 27, 2018
Completion date	March 29, 2019

View Details

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