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Monitoring Devices in Prediction of Fluid Responsiveness in Severe Sepsis and Septic Shock

Septic Shock Clinical Trial

Official title:
Comparison of the Accuracy of Monitoring Devices in Prediction of Fluid Responsiveness in Severe Sepsis and Septic Shock

Clinical Trial Summary

Comparison of noninvasive cardiac output monitor (NICOM, Cheetah Medical) with Edwards FloTrac minimally-invasive cardiac output monitor in predicting fluid responsiveness in sepsis and septic shock.

Clinical Trial Description

Study will evaluate ability of passive leg raise test to predict fluid responsiveness in patients in septic shock, on vasopressors, using both the NICOM and FloTrac devices. An increase in CI, SVI, or Pulse Pressure of >10% in response to the passive leg raise will be considered a positive passive leg raise test, and the same indicators will be considered a significant response to a fluid challenge with either crystalloids or colloids.Each device will be evaluated independently, but simultaneously. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02972827
Study type Interventional
Source Santa Barbara Cottage Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date May 2015
Completion date May 2022
View Details
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