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Clinical Trials/NCT01488370
NCT01488370
Completed
Not Applicable

A Comparison of the Glidescope® Video Laryngoscope and the Storz DCI® Video Laryngoscope for Endotracheal Intubation in Children Younger Than Two Years of Age

Loma Linda University2 sites in 1 country65 target enrollmentNovember 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endotracheal Intubation
Sponsor
Loma Linda University
Enrollment
65
Locations
2
Primary Endpoint
Measurement of Time to Intubation Will Begin at the Time of Mouth Opening and End With the Removal of the Tip of the Laryngoscope Blade From the Patient's Mouth After Successful Endotracheal Intubation.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This is a prospective randomized clinical study to be performed in pediatric patients under the age of 2 years who are undergoing surgical procedures requiring endotracheal intubation. Time to endotracheal intubation will be compared between patients intubated using a GlideScope® video laryngoscope, those intubated with a Storz DCI® video laryngoscope, and those intubated by standard direct laryngoscopy. The study hypothesis is that the time to endotracheal intubation will be decreased in the Storz DCI® video laryngoscope group when compared to the GlideScope® video laryngoscope group and standard laryngoscopy.

Registry
clinicaltrials.gov
Start Date
November 2011
End Date
July 2015
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Elizabeth Ghazal

MD

Loma Linda University

Eligibility Criteria

Inclusion Criteria

  • Pediatric patients under the age of 2 years undergoing surgeries requiring endotracheal intubation at LLUMC will be eligible for participation in this study

Exclusion Criteria

  • Children with increased pulmonary aspiration risk;
  • Prior documentation of difficult endotracheal intubation;
  • Those that lack legal representative consent

Outcomes

Primary Outcomes

Measurement of Time to Intubation Will Begin at the Time of Mouth Opening and End With the Removal of the Tip of the Laryngoscope Blade From the Patient's Mouth After Successful Endotracheal Intubation.

Time Frame: Less than one day, representing the day of surgery and period of endotracheal intubation during induction of general anesthesia

Secondary Outcomes

  • Successful Intubation After Three Laryngoscopy Attempts(Less than one day, representing the day of surgery and period of endotracheal intubation during induction of general anesthesia.)
  • Successful Intubation After One Laryngoscopy Attempt(Less than one day, representing the day of surgery and period of endotracheal intubation during induction of general anesthesia.)
  • Successful Intubation After Two Laryngoscopy Attempts(Less than one day, representing the day of surgery and period of endotracheal intubation during induction of general anesthesia.)
  • Successful Intubation After Four Laryngoscopy Attempts(Through endotracheal intubation during induction of general anesthesia, an average of 10 minutes)

Study Sites (2)

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