Cardiac Output Monitoring in Critically Ill Patient Undergoing Intubation

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Mayo Clinic

Status

Completed

Conditions

Hypotension

Treatments

Device: NICOM (Non invasive cardiac output monitor)

Study type

Observational

Funder types

Other

Identifiers

NCT03525743
16-006354

Details and patient eligibility

About

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

Full 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.

Enrollment

28 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

28 participants in 1 patient group

Patients undergoing intubation
Description:
Adhesive gel pads will be placed on patient to measure continuous cardiac output and to calculate stroke volume variation. Other physiologic data will be analyzed in real time using the NICOM (Non invasive cardiac output monitor) device.
Treatment:
Device: NICOM (Non invasive cardiac output monitor)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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