Define the capability and reliability of the PulmoVista® 500 (PV500) to detect changes in global and regional ventilation and perfusion.
The results of this study will help defining the capability and reliability of PulmoVista® 500 (PV500) to detect changes in both global and regional ventilation and perfusion. As this is a non-invasive, observational trial, neither a positive nor a negative impact on the actual study participants is expected. The results will, however, improve the knowledge about the electrical impedance tomography (EIT) technology and thus aid the use of this technology for the benefit of future patients.
Study Type
OBSERVATIONAL
Enrollment
22
Monitoring of Ventilation and Perfusion with the PulmoVista 500 during clinical routine. No medical interventions required
University Medical Center Göttingen
Göttingen, Germany
Assess regional distribution of pulmonary perfusion
The capability of PulmoVista® 500 for assessing regional distribution of pulmonary perfusion based on pulsatility signals and based on indicator dilution and changes at different points in time during varying states of regional ventilation will be evaluated.
Time frame: within 24 hours
Assess hemodynamic parameter cardiac output
The capability of PulmoVista® 500 for assessing cardiac output (relative values compared to reference given in l/min) will be explored.
Time frame: within 24 hours
Assess hemodynamic parameter heart rate
The capability of PulmoVista® 500 for assessing heart rate (1/min) will be explored.
Time frame: within 24 hours
Assess hemodynamic parameter stroke volume variability
The capability of PulmoVista® 500 for assessing stroke volume variability (relative value in % for 30 seconds compared to reference given in ml) will be explored.
Time frame: within 24 hours
Assess oxygenation status
The capability PulmoVista® 500 for assessing the oxygenation status from both the regional distribution of alveolar ventilation and the regional distribution of pulmonary perfusion will be explored.
Time frame: within 24 hours
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