Clinical validation during anesthesia of the Dräger PulmoVista 500 monitor.
- Conditions
- Mechanical ventilation, position, One-lung ventliation, atelectasis, anesthesia, airway devices
- Registration Number
- NL-OMON20301
- Lead Sponsor
- Z BrusselLaarbeeklaan 101 1090 JetteBelgium
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 160
Inclusion Criteria
Adult patients scheduled for general surgery without major heart, liver or kidney disordes.
Exclusion Criteria
Patients < 18Y and patients with major heart, liver or kidney disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occurence of ateclestasis during anesthesia with different ventilatory modes and devices will be investigated and the best ventilatory device and method described.
- Secondary Outcome Measures
Name Time Method Changes of haemodynamics 20 % beyond baseline measurements, or hypoxia with hemoglobin oxygen saturation below 90 %will be reported.