Influence of the timing of insertion of an Ambu® AuraGainTM laryngeal mask on the primary success rate in patients with elective anesthesia - a monocentric, prospective, randomized and single-blinded study
Not Applicable
- Conditions
- Various diseases, securing the airway as part of an elective operation in different specialist areas
- Registration Number
- DRKS00028989
- Lead Sponsor
- Klinik für Anästhesiologie und IntensivmedizinMedizinische Hochschule Hannover
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 280
Inclusion Criteria
Patients = 18 years of age who receive a planned airway management with a LAMA as part of an elective operation with anesthesia.
Written consent to study participation
Exclusion Criteria
Primary planned endotracheal intubation;
Patients whitout overnight fasting;
Pregnancy;
Patients unable to consent without a supervisor
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of success rate of LAMA placement depending on the time of insertion (Group 1 (unconsciousness) versus Group 2 (intermediate ventilation)).
- Secondary Outcome Measures
Name Time Method umber of further attempts until success<br>Number and type of complications<br>Oropharyngeal Leakage Pressure of the LAMA