A prospective,randomized comparative study of clinical efficacy of Ambu aura gain v/s LMA proseal in adult patient undergoing elective surgery under general anaesthesia
Phase 2
- Registration Number
- CTRI/2023/06/053536
- Lead Sponsor
- lrm medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA grade I and grade II Patients. 2. Age- 18 to 65 years of either sex. 3. Patients undergoing surgery under general anaesthesia. 4. Patient willing to give informed and written consent. 5. Mouth opening - Malampatti grade I/II. 6. Posted for surgery of short duration( <1-2hrs). 7. Posted for surgery requiring supine position only.
Exclusion Criteria
Patient refusal cervical spine pathology
Anticipated difficult airway anticipated surgery greater than 3 hours
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oropharyngeal seal pressureTimepoint: Once after insertion of supraglottic airway device
- Secondary Outcome Measures
Name Time Method Any displacement of deviceTimepoint: After extubation;Any injuryTimepoint: After extubation;Blood staining of deviceTimepoint: After extubation;Diastolic blood pressureTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;heart rateTimepoint: baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;HoarsenessTimepoint: After extubation;oxygen saturationTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;Post-op complication like sorethroatTimepoint: After extubation;Systolic blood pressureTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.