J96.0 E66.0
Conditions
Interventions
Group 1: Control group (spontaneous breathing without Flow Limiter)
Group 2: Intervention group (spontaneous breathing with Flow Limiter)
Sponsors
Department of Anesthesiology and Critical Care University Medical Center Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age = 18 years, elective surgery in general anesthesia, physical status according to the ASA I-III, written informed consent, BMI > 30 kg/m.^-2
Exclusion criteria
Exclusion criteria: Age < 18 years, COPD (GOLD 3, clinical presentation), pregnancy, emergency procedure, rejection of participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative oxygen saturation (pulse oximetry). | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of postoperative pulmonary complications (radiologic, laborchemistry, microbiological examinations), respiratory and hemodynamic variables, blood gas test | — |
Countries
Germany
Contacts
Public ContactJonas Weber
Department of Anesthesiology and Critical Care University Medical Center Freiburg
Outcome results
None listed