Trials / Completed
CompletedNCT01876940
Comparison of Fiberoptic Intubation With Fiberoptic Intubation Through an Air-Q Intubating Laryngeal Airway in Infants and Small Children
A Randomized Comparison of Free-handed Fiberoptic Intubation Compared With Fiberoptic Intubation Through an Air-QTM Intubating Laryngeal Airway in Children Less Than Two Years of Age: Does Operator Experience Affect Time to Successful Tracheal Intubation?
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Ann & Robert H Lurie Children's Hospital of Chicago · Academic / Other
- Sex
- All
- Age
- 1 Day – 2 Years
- Healthy volunteers
- Accepted
Summary
The goal of this prospective randomized study is to compare the effect of operator experience on the ability to use fiberoptic-guided intubation in children less than two years old, with and without the use of an air-Q as a conduit. The question the investigators are trying to answer is: Does the operator experience make a significant difference in the time for successful fiberoptic guided tracheal intubation with and without the use of an air-Q intubating laryngeal airway?
Detailed description
The aim of this study is to compare the effect of operator experience on the ability to use fiberoptic-guided intubation in children less than two years old, with and without the use of an air-Q as a conduit. The ease and time for placement of the air-Q, fiberoptic grade of laryngeal view, time for fiberoptic tracheal intubation, and peri-operative complications will also be assessed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | air-Q, followed by fiberoptic intubation | |
| DEVICE | Free-hand Fiberoptic Intubation | Fiberoptic tracheal intubation will be performed without use of the air-Q and timed. Laryngeal grade of view will also be assessed |
Timeline
- Start date
- 2013-06-01
- Primary completion
- 2013-07-01
- Completion
- 2013-07-01
- First posted
- 2013-06-13
- Last updated
- 2013-07-30
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01876940. Inclusion in this directory is not an endorsement.