Viability of Pulsioflex Monitoring in ICU

Status Completed

Clinical Trial Summary

Clinical Trial Description

Goal of the Study is to Study the precision of semi-invasive cardiac index monitoring by means of the ProAQT (PULSION Medical Systems SE) sensor, whereby the pulmonary artery catheter will serve as gold standard. Measurements will be performed contemporaly with both devices every 4 hours and all clinical and hemodynmaic parameters will be recorded, including but not limited to central venous pressure, wege pressure, mechanical ventilation pressures, blood pressures, volume balance as well as vasoaktive medikation doses. This precise evaluation shall serve to evaluate the precision of the ProAQT to estimate the cardiac index under different clinical situation in the intensive care unit. A precision difference of below 30% between both methods will be regarded as clinically irrelevant, suggesting equipoise between both methods. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04911985
Study type	Observational
Source	University of Zurich
Contact
Status	Completed
Phase
Start date	July 1, 2015
Completion date	August 30, 2019

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