Clinical Trials Directory

Trials / Completed

CompletedNCT01535742

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago · Academic / Other
Sex
All
Age
1 Month – 6 Years
Healthy volunteers
Accepted

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.

Detailed description

The goal of this prospective randomized study is to compare the Ambu Aura-i and air-Q ILA in children with normal airway anatomy, in order to evaluate the effectiveness of fiberoptic tracheal intubation through these two devices. The ease of placement, fiberoptic grade of laryngeal view, time to tracheal intubation, time for device removal after intubation, and peri-operative complications will also be assessed.

Conditions

Interventions

TypeNameDescription
DEVICEAmbu Aura-i size 1.5Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed
DEVICEair-Q ILA size 1.5Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed
DEVICEAmbu Aura-i size 2Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed
DEVICEair-Q ILA size 2Device will be placed and fiberoptic tracheal intubation will be performed and timed. Laryngeal grade of view will also be assessed

Timeline

Start date
2012-02-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2012-02-20
Last updated
2012-06-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01535742. Inclusion in this directory is not an endorsement.