Incidence of postoperative pharyngolaryngeal adverse events with LMA Supreme at high and low intracuff pressures
Not Applicable
Recruiting
- Conditions
- Not Applicable
- Registration Number
- KCT0000334
- Lead Sponsor
- Konkuk University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Patients undergoing laparoscopic surgical procedures were enrolled and written informed consent was obtained.
Exclusion Criteria
Patients were excluded if the following criteria present: 1)known or predicted difficult airway, 2)vocal cord paralysis, 3)recent history of respiratory infection (within 1 month), 4)neurological deficits or psychiatric disorders, 5)history of drug abuse, 6)receiving current medications, 7)allergy to egg or soybean oil, 8)contraindications for use of LMA.
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method sore throat
- Secondary Outcome Measures
Name Time Method dysphagia; dysphonia