Comparison of Fiberoptic Intubation With Fiberoptic Intubation Through an Air-Q Intubating Laryngeal Airway in Infants and Small Children
Completed · Not applicable
Conditions studied: Fiberoptic Intubation in Children
In brief
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?
Key facts
- Study ID
- NCT01876940
- Run by
- Ann & Robert H Lurie Children's Hospital of Chicago
- People needed
- 80
- Starts
- 2013-06-01
- Expected to finish
- 2013-07-01
- Last updated by the study team
- 2013-07-30
Who can join
Age: 0 and older, up to 2. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy (ASA I to III) children who will be intubated as part of their general anesthesia plan for their scheduled surgeries
- Age 1 month - 2 years
- Weight 1-20 Kg
You may not qualify if…
- Children with active respiratory infection
- Known history of difficult mask ventilation
- Diagnosis of a congenital syndrome associated with difficult airway management
- Airway abnormalities (e.g., laryngomalacia, subglottic stenosis).
Where it is running
- Ann & Robert H. Lurie Children's Hospital of Chicago — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.