Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Mechanical Ventilation
  • Ventilation Perfusion Mismatch
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 80 years
Gender
Both males and females

Description

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...

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.

Tracking Information

NCT #
NCT04249414
Collaborators
  • University of Göttingen
  • Prof. Dr. med. Imhoff
Investigators
Principal Investigator: Onnen Mörer, Prof. Dr. Centre of Anaesthesiology University Medical Center Göttingen Study Director: Michael Quintel, Prof. Dr. Centre of Anaesthesiology University Medical Center Göttingen