Comparison of two airway devices (Baska and Gnana II) in patients receiving general anaesthesia for surgery.
Not Applicable
- Conditions
- Health Condition 1: K800- Calculus of gallbladder with acutecholecystitisHealth Condition 2: K358- Other and unspecified acute appendicitisHealth Condition 3: K409- Unilateral inguinal hernia, without obstruction or gangreneHealth Condition 4: S529- Unspecified fracture of forearm
- Registration Number
- CTRI/2020/03/024040
- Lead Sponsor
- Government Medical College and Hospital Sector Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age group between 18 to 60 years
2.American Society of Anaesthesiologist (ASA) physical status I and II.
3.Patients scheduled for elective surgery under general anaesthesia (Duration of surgery 2 ± 0.5 hrs)
Exclusion Criteria
1.Patients with anticipated difficult airway (Airway Difficulty Score >8).
2.Patients with upper respiratory tract infection
3.Patients with increased risk of regurgitation and aspiration of gastric content
4.Patients with a body mass index (BMI) > 35 kg.m.-2
5.Patients with past history of radiotherapy to the neck involving the hypopharynx
6.Patients undergoing surgeries involving neck and oral cavity
7.Pregnant patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the oropharyngeal leak pressure of Baska mask airway with Gnana laryngeal airway II in paralysed patients undergoing elective surgery with controlled ventilation.Timepoint: Immediately after the placement of device at 0 minute and 10minutes.
- Secondary Outcome Measures
Name Time Method To evaluate the efficacy of Baska mask airway with Gnana laryngeal airway II for <br/ ><br>device insertion success, <br/ ><br>ease of device insertion, <br/ ><br>fibreoptic visualization of glottis, <br/ ><br>hemodynamic,ventilatory parameters, <br/ ><br>amount of oropharyngeal secretions sucked and side effects if any.Timepoint: 1.Ease of insertion,fiberoptic visualization-will be observed immediately after the placement of the device at 0 minute. <br/ ><br>2. Haemodynamic and ventilatory parameters-at Time points ((minutes) 1,2,3,4,5 and 10 minutes.