Randomized multi-centric trial comparing the classical double lumen endobronchial tube and the ViviSight double lumen endobronchial tube for airway management during thoracic surgery
Not Applicable
Recruiting
- Conditions
- ung cancer, pneumothoraxC34.9J93.9Bronchus or lung, unspecifiedPneumothorax, unspecified
- Registration Number
- DRKS00010090
- Lead Sponsor
- Klinik für AnästhesiologieUniversitätsmedizin Göttingen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
female with body hight of 150-175cm, male with body hight of 165-185cm
Exclusion Criteria
Body size others than mentioned
Expected difficult airway
Refusal of written informed consent
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time from start to finish of anesthesia induction, need for intraoperative control tube position<br>Feedback directly from surgeon/anesthesist with questionnaire<br>Feedback from Patient until 90minutes after surgery as well as first day following surgery regarding airway morbidity and wound pain.
- Secondary Outcome Measures
Name Time Method costs per anesthesia,<br>Evaluation of intraoperative conditions by surgeon, <br>Evaluation of conditions by anesthesist