A clinical trial to study two Airway Equipments I-Gel and Laryngeal Tube Suction for Anesthetised patients
Not Applicable
- Conditions
- Health Condition 1: null- Study is conducted on patients undergoing elective surgery under General anesthesia.
- Registration Number
- CTRI/2010/091/002993
- Lead Sponsor
- Institution
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ASA I , II
Elective surgery under general anesthesia
Exclusion Criteria
Airway abnormalities
Difficult Intubation
Risk of aspiration
Mouth opening less than 3cm
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Efficacy of ventilation between cuffed and uncuffed supraglottic airway devicesTimepoint: Duration of surgery
- Secondary Outcome Measures
Name Time Method Any risk of aspiration or throat problems following surgeryTimepoint: Post operative followup for 24 hrs