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A comparative study to assess the safety and efficacy of Ambu Aura Gain versus I-Gel ( supraglottic airway devices) in adult patients under General Anaesthesia

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/09/057684
Lead Sponsor
Department of Anaesthesia MMCRI Mysore
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All ASA grade I and II patients between 18-50 years of both sex.

Elective surgeries under general anaesthesia with controlled ventilation.

Body mass index 25-28 Kg/m2.

Duration of surgery <2hrs.

Exclusion Criteria

Age <18 years and > 50 years.

All ASA grade III and above.

Mallampatti grade 3 and above.

Emergency surgeries.

Head and neck surgeries.

Patients with decreaesed mouth opening.

Patients with increased risk of aspiration.

Patients with BMI >28 Kg/m2.

Patients with abnormal or distorted anatomy of pharynx.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Oropharyngeal leak pressure <br/ ><br>Ease of Insertion & number of attempts. <br/ ><br>Time taken for insertion. <br/ ><br>Ease of insertion of Ryles tube . <br/ ><br>Fibreoptic bronchoscopic grading.Timepoint: 10 min <br/ ><br> <br/ ><br>2 min <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Haemodynamic response, SpO2, EtCO2 <br/ ><br>Incidence of post operative complicationsTimepoint: 2 hrs <br/ ><br>24hrs.
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