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Comparison of ease of intubation through I-gel versus Ambu Auragain

To compare the ease of intubation through an I-gel versus Ambu Auragain : A prospective randomised study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/031714
Enrollment
100
Registered
2021-03-04
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: O- Medical and Surgical

Interventions

Intervention1: I-gel: Ease of intubation through this supraglottic airway device. Control Intervention1: Ambu Auragain: Ease of intubation through this device and compared with intubation through I-ge

Sponsors

Government Medical College Patiala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I/II Age group 20-60 years

Exclusion criteria

Exclusion criteria: Anticipated difficult airway History of gastroesophageal reflux disease Any contraindications to use of muscle relaxants Increased risk of aspiration Oropharyngeal pathology Poor lung compliance

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of I-gel and AAG in terms of number of attempts taken for effective supraglottic airway device placement,time to achieve effective ventilation after supraglottic airway device placement,number of attempts for endotracheal intubation,intubating time and number of cases in which fiberoptic bronchoscope is requiredTimepoint: Time taken for supraglottic Airway Device(SAD) placement. Time taken for intubation through SAD. Total intubation time.

Secondary

MeasureTime frame
To compare haemodynamics and complications with the use of I-gel and AAG as conduit for endotracheal intubationTimepoint: To compare haemodynamics with the use of I-gel and AAG as conduit for endotracheal intubation Vitals(Heart Rate,Blood pressure,Mean arterial pressure,sPO2,ETCO2) will be recorded till the end of surgery and recorded for every 1 minute for first 10 minutes and every 5 minutes for 30 minutes

Countries

India

Contacts

Public ContactDr Tripat Kaur Bindra

government medical college and hospital patiala

tripat_noori@yahoo.co.in9501017040

Outcome results

None listed

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