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Clinical validation during anesthesia of the Dräger PulmoVista 500 monitor.

Clinical validation during anesthesia of the Dräger PulmoVista 500 monitor.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20301
Enrollment
160
Registered
2012-03-06
Start date
2012-03-15
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mechanical ventilation, position, One-lung ventliation, atelectasis, anesthesia, airway devices

Interventions

Monitoring of lungs using the PulmoVista 500 lung monitor during anesthesia in different conditions: 1. Comparison of airway devices: Spontaneously breathing patients, ETT and general anesthesia, LM
2. During laparoscopic surgery in three classical positions – supine, Trendelenburg and reverse Trendelenburg
3. During two and one-lung ventilation in the supine position with closed chest
4. During High frequency jet ventilation versus one-lung ventilation.

Sponsors

UZ Brussel Laarbeeklaan 101 1090 Jette Belgium
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients scheduled for general surgery without major heart, liver or kidney disordes.

Exclusion criteria

Exclusion criteria: Patients < 18Y and patients with major heart, liver or kidney disorders.

Design outcomes

Primary

MeasureTime frame
Occurence of ateclestasis during anesthesia with different ventilatory modes and devices will be investigated and the best ventilatory device and method described.

Secondary

MeasureTime frame
Changes of haemodynamics 20 % beyond baseline measurements, or hypoxia with hemoglobin oxygen saturation below 90 %will be reported.

Contacts

Public ContactVeerle Mossevelde, van

Laarbeeklaan 101

veerle.vanmossevelde@uzbrussel.be+32 (0)2 4763134

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)