GlideScope Video Laryngoscope Versus Fiberoptic Intubation
Summary
Following informed consent, patients will be randomly assigned to oral fiberoptic intubation or to oral intubation using the GlideScope Video Laryngoscope. Following the induction of general anesthesia a sealed envelope would be opened to reveal the technique to be used. A stop watch will be started at the beginning of the procedure. At the completion of intubation the stop watch will be stopped and the time recorded along with other data. Based on a sample size estimation process, it is the investigators plan to study fifty patients. The two techniques will be compared in terms of the average time needed to place the endotracheal tube and studied using a two-sided T-Test with a significance level of 0.05. To ensure comparability between the two methods, all intubators will be required to have at experienced at least 10 uses of the GlideScope and 10 uses with fiberoptic intubation.
Study Design
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care
Conditions
Oral Intubation
Intervention
Intubation with Fiberoptic laryngoscope, GlideScope® Video Laryngoscope
Location
Cleveland Clinic Foundation
Cleveland
Ohio
United States
44195
Status
Completed
Source
Outcomes Research Consortium
Results (where available)
Links
- Source: http://clinicaltrials.gov/show/NCT01091948
- Information obtained from ClinicalTrials.gov on July 15, 2010
Published on BioPortfolio: 2014-07-24T14:06:47-0400
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PubMed Articles
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