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COMPLETED
NCT01535742
NA

Ambu Aura-i and Air-Q Intubating Laryngeal Airways as a Conduit for Tracheal Intubation in Children

Sponsor: Ann & Robert H Lurie Children's Hospital of Chicago

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine whether there is a clinically relevant difference in time to tracheal intubation when using fiberoptic bronchoscope as a guide to intubate through the Ambu Aura-i or air-Q ILA.

Official title: Prospective Randomized Comparison of the Ambu Aura-i and Air-Q Intubating Laryngeal Airways as a Conduit for Tracheal Intubation in Children

Key Details

Gender

All

Age Range

1 Month - 6 Years

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2012-02

Completion Date

2012-04

Last Updated

2026-10-16

Healthy Volunteers

Yes

Interventions

DEVICE

Ambu Aura-i size 1.5

Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed

DEVICE

air-Q ILA size 1.5

Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed

DEVICE

Ambu Aura-i size 2

Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed

DEVICE

air-Q ILA size 2

Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed

Locations (1)

Childrens Memorial Hospital

Chicago, Illinois, United States