Baska mask versus Proseal laryngeal mask for reduction of laryngopharyngeal morbidity following elective surgery.
Recruiting
- Conditions
- Patients undergoing elective surgical procedure under general anesthesia with a supraglottic airway device
- Registration Number
- NL-OMON29377
- Lead Sponsor
- Ministry of Health (Oman)PO Box 393 Postcode 113 Muscat, Sultanate of Oman
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
1. Patients who give informed consent;
2. Elective ambulatory surgery with an estimated duration of 30 to 60 minutes;
Exclusion Criteria
1. Predictors of or a history of difficult intubation;
2. Immobilized cervical spine;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sore throat score following the use of SADs. <br>(Score 0 = no complaints, score 1 = minimal sore throat, score 2 = moderate sore throat, score 3 = severe sore throat: never a SAD again).
- Secondary Outcome Measures
Name Time Method 1. Insertion time needed for placement of the SAD;<br /><br>2. Number of attempts needed to correctly place the SAD;<br /><br>3. Airway Sealing Pressure in cm H2O at 5 and 10 mins post-placement;<br /><br>4. Ease of removal;<br /><br>5. Blood on the device;<br /><br>6. Duration for which the device remained in the oropharynx.