Comparison of postoperation complication between Laryngeal Mask Airway and Endotracheal tube during low flow anesthesia with controlled ventilatio
Not Applicable
- Conditions
- dysphagia.dysphagia
- Registration Number
- IRCT201203042582N5
- Lead Sponsor
- research chancellor, tabriz university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
adult patients with ASA class I and II aging 20-60 years who are candidates for elective surgery
Exclusion criteria: possibility of air way problems, history of recent sore throat or a cold in the past 10 days, patients with latex allergy, patients with full stomach
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sore throat. Timepoint: every 6 hours until 24 hours. Method of measurement: asking from patient.;Cough. Timepoint: every 6 hours until 24 hours. Method of measurement: asking from patient.
- Secondary Outcome Measures
Name Time Method Dysphagia. Timepoint: every 6 hours until 24 hours. Method of measurement: asking from patient.