Evaluation of the i-gel supraglottic airway.
Completed
- Conditions
- 1. i-gel<br /> 2. supraglottic airway<br />3. laryngeal mask (larynx masker)<br />4. sore throat (keelpijn).
- Registration Number
- NL-OMON25310
- Lead Sponsor
- The Netherlands Cancer Institute - Antoni van Leeuwenhoek HospitalPlesmanlaan 1211066 CX Amsterdam
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 240
Inclusion Criteria
1. ASA 1-2;
2. Adults (age 18 to 80 years);
Exclusion Criteria
1. ASA 3 and above;
2. Below the age of 18 or above the age of 80;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparing the incidence of postoperative sore throat after 1, 24 and 48 hours.
- Secondary Outcome Measures
Name Time Method Comparing insertion and ventilation parameters, maximum seal power and fibre-optic evaluation of device position of the two supraglottic airway devices.