Comparison of Orophayrngeal seal pressure and peak airway pressure between Baska mask and I gel in patients undergoing laparoscopic surgeries.

Not yet recruiting

Conditions: Measurement and Monitoring,

Registration Number: CTRI/2023/08/056721

Lead Sponsor: Department of Anesthesiology and critical care

Brief Summary: Airway management is considered as an integral part of general anesthesia. Endotracheal

intubation has been considered as a conventional gold standard method for securing the airway

during GA.1 In the last few years , many supraglottic airway devices (SADs) have been

introduced in clinical practice. Supraglottic airway devices has changed the scenario from

’unable to intubate and ventilate’ to ’unable to intubate but able to ventilate’.1 These devices has

much importance for patients with difficult tracheal intubation or where intubation is

impossible. 1 Oropharygeal seal pressure and peak airway pressure is an important parameter

for safe use during laparoscopic surgeries.

In this study, we evaluated the performance of the baska mask , a new extraglottic airway

device (EAD) for use in anesthesia in adult patients undergoing a variety of surgical

interventions.

The purpose of this study is to compare the oropharyngeal seal pressure and peak airway

pressure between baska mask and I gel after creating pneumoperitoneum in laparoscopic

surgeries.

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 80

Inclusion Criteria

80 patients of either sex, aged 18â€“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.

Exclusion Criteria

Patient refusal to consent Obesity (body mass index â‰¥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
2.To determine peak airway pressure in baska mask & I-gel after creating	Measured at 1 min after induction, at 5 mins before and after creating pneumoperitoneum, and at 5 mins before and after deflation of pneumoperitoneum.
1.To determine oropharyngeal Seal Pressure in baska mask & I-gel after creating	Measured at 1 min after induction, at 5 mins before and after creating pneumoperitoneum, and at 5 mins before and after deflation of pneumoperitoneum.
pneumoperitoneum in patients undergoing laparoscopic surgeries.	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.	It is taken as the time from picking up the device till

Trial Locations

Locations (1): Maharaja Agrasen Medical College, Argoha, Hisar
🇮🇳
Hisar, HARYANA, India
Maharaja Agrasen Medical College, Argoha, Hisar
🇮🇳Hisar, HARYANA, India
Dr Shalini
Principal investigator
7982145046
shalini.verma1295@gmail.com