Comparing two devices named Ambu AuraGain and i Gel for general anaesthesia laparoscopic hernia repair surgery
Not Applicable
- Conditions
- Health Condition 1: N00-N99- Diseases of the genitourinary system
- Registration Number
- CTRI/2019/03/017940
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I and II, aged between 18-60years, scheduled to undergo laparoscopic inguinal hernia repair with anticipated surgical duration less than two hours
Exclusion Criteria
patients who refuse, have anticipated difficult airway( eg. mouth opening < 2 cm, Mallampati Grade III and IV, airway deformity), with BMI >30kg/m2, with history of obstructive sleep apnoea, pregnancy, lactating mothers, hepatic, renal or cardiac abnormality, alcoholism, diabetes, significant gastrointestinal disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the oropharyngeal leak pressures for the two devices, after insertion and after positioning and carboperitoneumTimepoint: After insertion and after positioning and 5 and 30 minutes after carboperitoneum
- Secondary Outcome Measures
Name Time Method To compare the time required for insertion, attempts, ease of gastric tube insertion, grade of fibreoptic glottic view and post-operative complications such as sore throat, nausea, vomiting etcTimepoint: Intraoperative period and upto 24 hours in the postoperative period