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Comparison of three supraglottic devices for airway management during laparoscopy

Comparative evaluation of AMBU Auragain, i-gel and LMA Proseal in patients undergoing laparoscopic cholecystectomy under general anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022367
Enrollment
60
Registered
2019-12-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K801- Calculus of gallbladder with othercholecystitis

Interventions

Intervention1: One of the three airway devices will be inserted.: After induction of anaesthesia one of the three airway devices will be inserted and the performance of the device will be compared Con

Sponsors

University College of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I/II Modified Mallampatti class I/II Scheduled for elective laparoscopic cholecystectomy under general anaesthesia

Exclusion criteria

Exclusion criteria: BMI > 30 kg/m2 Pregnant women Known or predicted difficult airway Known case of COPD, asthma or any other restrictive or obstructive respiratory pathology Patients at high risk for pulmonary aspiration

Design outcomes

Primary

MeasureTime frame
Oropharyngeal leak pressureTimepoint: After insertion of device Before CO2 insufflation Just after insufflation 15 mins after insufflation 30 mins after insufflation 45 mins after insufflation 60 mins after insufflation 75 mins after insufflation 90 mins after insufflation 105 mins after insufflation 120 mins after insufflation After deflation of abdomen

Secondary

MeasureTime frame
Ease of insertion Number of attempts for successful insertion Success rate in first attempt Maneuvers required for insertion Ease of insertion of gastric tube Timepoint: Once after successful insertion of device;Haemodynamic variables and ventilatory parametersTimepoint: Preoperatively Baseline At the time of insertion of device Thereafter, the readings will be taken at 1,3,5 & 10 mins interval At the time of removal of device 5 mins after removal of device

Countries

India

Contacts

Public ContactPriyanka Anand

University College of Medical Sciences

sujatac462@gmail.com9625900800

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026