Awake fiberoptic intubation Respiratory
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Anaesthesiology residents, consultant anaesthetist and anaesthetic nurses
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Goals reached, duration, rotation, distance, direction changes and impact including an assessment of own skills as measured by the ORSIM simulator at baseline, 6 months and 12 months 2. Amount of flexible bronchoscopic intubations, using a visual analogue score (VAS) at baseline, 6 months and 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
Netherlands