Comparison between I gel, ProSeal and Classical Laryngeal Mask Airways in Paediatrics: randomised controlled trial

Not Applicable

• Conditions: Paediatrics; Airway management

• Registration Number: PACTR201702001718176
• Lead Sponsor: Fayoum University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-07-20
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

ASA physical status I and II patients.
Undergoing elective surgery (30-90 min) duration, in supine position.
In the period between January 2015 and June 2015.
Age range between 5to 15 years.

Exclusion Criteria

Patients with Syndromes known to have difficult airway.
Patients with gross upper airway pathology or anatomical anomaly.
Patients at risk of aspiration.
History of lung diseases

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sucessful management of the airway

Secondary Outcome Measures

Name	Time	Method
the time to successful insertion was measured from the moment the facemask was removed until the first capnography upstroke after insertion of the device.;ease of insertion;Fiberoptic view;Oropharyngeal leak pressure;Peak airway pressure;Complications