An Evaluation of Efficacy of the GlideScope Cobalt Video Baton for Intubation on Children Weighing Less Than 10 Kilograms
|ClinicalTrials.gov Identifier: NCT00935636|
Recruitment Status : Completed
First Posted : July 9, 2009
Last Update Posted : June 21, 2013
|Condition or disease|
Neonates and infants requiring endotracheal intubation and in which the attending anesthesiologist decided to use the CGS-CVB will be included in this observational study. Data will be collected by one of the investigators or the research assistant/coordinator and recorded on a data sheet The data from these forms will be then entered by the investigator or research assistant/coordinator into a database maintained only for this study.
The decision of using the GS-CVB is at the discretion of the attending anesthesiologist. Consequently if consent would be required the anesthesiologist might feel compelled or biased to use the device against his will. This will also require that all possible patients's should be consented which will put a serious strain on the study personal.
|Study Type :||Observational|
|Actual Enrollment :||200 participants|
|Official Title:||An Evaluation of Efficacy of the GlideScope Cobalt Video Baton for Intubation on Children Weighing Less Than 10 Kilograms|
|Study Start Date :||May 2009|
|Actual Primary Completion Date :||September 2011|
|Actual Study Completion Date :||October 2011|
- Time to intubation [ Time Frame: From the time the ETT enters the mouth until end-tidal carbon dioxide is detected on the monitor screen ]
- The time to laryngoscopic views, number of attempts, and the success rate [ Time Frame: from the time the device enters the mouth until the best view is acknowledged. ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00935636
|United States, Texas|
|Chlidren's Medical Center Dallas|
|Dallas, Texas, United States, 75235|
|Principal Investigator:||Peter Szmuk, MD||UT Southwestern|