Intubation using VieScope, video laryngoscopes and conventional laryngoscopy in simulated severe hemorrhage in the airways - a randomized, controlled model study
Not Applicable
Recruiting
- Conditions
- difficult airway
- Registration Number
- DRKS00023412
- Lead Sponsor
- niklinik Köln - Anästhesie und operative Intensivmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- 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
• Persons incapable of giving consent
• Age under 18, age over 65
• Rejection of the test subjects
• Pregnancy, breastfeeding
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 <br>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)