Comparison of Orophayrngeal seal pressure and peak airway pressure between Baska mask and I gel in patients undergoing laparoscopic surgeries.
- Conditions
- Health Condition 1: 4- Measurement and Monitoring
- Registration Number
- CTRI/2023/08/056721
- Lead Sponsor
- Department of Anesthesiology and critical care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
80 patients of either sex, aged 18–60 years, belonging to American Society of Anaesthesiologists (ASA) physical status class I and II presenting for laparoscopic surgery
under general anaesthesia will be included in the study.
Patient refusal to consent
Obesity (body mass index =30 kg/m2)
Pregnancy
Known or predicted difficult airway (Mallampati grade 3/4, mouth opening < 3 cm,
thyromental distance < 6cm , positive upper lip bite test)
Reduced lung compliance
High risk for pulmonary aspiration (non fasted, gastroesophageal reflux disease)
Patients with known cardiorespiratory illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To determine oropharyngeal Seal Pressure in baska mask & I-gel after creating <br/ ><br>pneumoperitoneum in patients undergoing laparoscopic surgeries. <br/ ><br>2.To determine peak airway pressure in baska mask & I-gel after creating <br/ ><br>pneumoperitoneum in patients undergoing laparoscopic surgeries.Timepoint: Measured at 1 min after induction, at 5 mins before and after creating pneumoperitoneum, and at 5 mins before and after deflation of pneumoperitoneum.
- Secondary Outcome Measures
Name Time Method To determine ease of insertion & time of insertion in baska mask and I gel.Timepoint: It is taken as the time from picking up the device till <br/ ><br>appearance of a capnograph waveform. The insertion time is the sum of all the attempts taken.It will be noted using a stopwatch by an independent assessor.