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Clinical Trial Summary

The aim is to describe the physiological background for PLR and the interpretation of a PLR manoeuvre. The protocol entails the measurement of stroke volume (SV) at baseline (semirecumbent patient position), during PLR and after returning to semirecumbent position. Simultaneously blood pressure (BP), pulse rate (PR), pulse oximetric saturation (SpO2) and ECG are recorded. The procedure is performed in ten normal subjects, ten patients recruited in the cardiology outpatient department and ten critically ill patients under analgosedation in the ICU. Analysis includes changes in measured variables and heart rate variability in the frequency domain during the three phases of the experiment.


Clinical Trial Description

See above ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03454802
Study type Interventional
Source Region MidtJylland Denmark
Contact
Status Completed
Phase N/A
Start date September 1, 2018
Completion date October 1, 2020

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