Intubation using VieScope, video laryngoscopy and conventional laryngoscopy in simulated difficult airway - a randomized, controlled model study
Not Applicable
- Conditions
- DIFFICULTAIRWAY
- Registration Number
- DRKS00024968
- Lead Sponsor
- niklinik Köln - Anästhesie und operative Intensivmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 35
Inclusion Criteria
• male or female volunteers
• medical healthcare professionals
• Age between 18 and 65 years
• Prior written consent following written and verbal information from an investigator
Exclusion Criteria
• male or female volunteers
• medical healthcare professionals
• Age between 18 and 65 years
• Prior written consent following written and verbal information from an investigator
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Tube position: tracheal, bronchial, oesophageal (primary endpoint), immediately after Intubation, validated by insufflation of the test lung
- Secondary Outcome Measures
Name Time Method 2. Correct tube position for the first intubation - first pass (secondary endpoint)<br>3. Time to Intubation (Secondary Endpoint)<br>4. Time to first ventilation (secondary endpoint)