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A Randomised Comparative study to evaluate the performance of Ambu Auragain and the Laryngeal Mask Airway Supreme

A Randomised Comparative study to evaluate the performance of Ambu Auragain and the Laryngeal Mask Airway Supreme in Adult patients for Elective surgeries under General Anaesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055390
Enrollment
120
Registered
2023-07-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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: Anaesthesia- Supraglottic Airway Device: This study compares the insertion of device,OLP, ease of NGT insertion, hemodynamic stability and any complications Intervention2: Insertion of

Sponsors

JJM Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Duration of surgeries less than 2 hours ASA I and II Posted for elective surgery under general anaesthesia in supine position

Exclusion criteria

Exclusion criteria: Patients with predicted difficult airway Patients with any pathology in neck, upper respiratory or alimentary tract BMI more than 30kg/me Patients with history of obstructive sleep apnea,lung diseases or bleeding disorders Patients with full stomach or history of oesophageal reflux Pregnancy

Design outcomes

Primary

MeasureTime frame
Number of attempts, time taken for insertion(in seconds) and ease of insertion Oropharyngeal leak pressure(in cm H2O) Ease of insertion of Nasogastric tube Hemodynamic changes(heart rate, saturation and blood pressure) Timepoint: Hemodynamic changes(heart rate, saturation and blood pressure)at 1min, 5min and 10 min after Supraglottic Airway Device insertion

Secondary

MeasureTime frame
Intraoperative desaturation or laryngospasm Blood stain on device during withdrawal Postoperative sore throat, hoarseness or dysphagiaTimepoint: 1 hour and 6 hours postoperatively

Countries

India

Contacts

Public ContactJSAnmol

JJM Medical College

drsumakv@gmail.com9886783103

Outcome results

None listed

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