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Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01683526
First Posted: September 12, 2012
Last Update Posted: October 20, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Beth Israel Medical Center
September 6, 2012
September 12, 2012
May 23, 2014
June 25, 2014
October 20, 2014
August 2012
April 2013   (Final data collection date for primary outcome measure)
First Pass Success Rate [ Time Frame: From begining of intubation to verification. Less then 5 minutes approximatly ]
Same as current
Complete list of historical versions of study NCT01683526 on ClinicalTrials.gov Archive Site
  • Severe Desaturation [ Time Frame: For 10 minutes post intubation ]
    sat <80%
  • Hypotension [ Time Frame: For 10 minutes post intubation ]
    SBP<70
  • Cardiac Arrest [ Time Frame: For 1 hour post intubation ]
  • Complications of Intubation [ Time Frame: For 10 minutes post intubation ]
    Complications of intubation including aspiration, vomiting, esophageal intubation,and dental injury.
Same as current
Not Provided
Not Provided
 
Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope
Safety and Efficacy of Endotracheal Intubation by Pulmonary Critical Care Physicians in Critically-Ill Patients Using Glidescope Video-Laryngoscope
The safety and efficacy of a video-laryngoscope as a primary intubation tool in urgent endotracheal intubation of critically-ill patients has not been well-described in the literature. This study will answer whether using a VL will impact on the efficacy and safety of intubation compared with a traditional direct laryngoscopy.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Respiratory Failure
  • Procedure: Direct laryngoscopy
    Other Name: standard laryngoscope
  • Device: Video laryngoscopy (Glidescope)
    Other Name: Glidescope Video Laryngoscope
  • Active Comparator: Direct laryngoscopy
    Intubation will be done using direct laryngoscopy
    Intervention: Procedure: Direct laryngoscopy
  • Active Comparator: Video laryngoscopy
    Intubation will be done using video laryngoscopy
    Intervention: Device: Video laryngoscopy (Glidescope)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
117
April 2013
April 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • All patients undergoing urgent endotracheal intubation by a pulmonary critical care medicine physician

Exclusion Criteria:

  • Difficult airway
  • Oxygen saturation < 92% despite adequate mask ventilation
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01683526
139-12
No
Not Provided
Not Provided
Beth Israel Medical Center
Beth Israel Medical Center
Not Provided
Principal Investigator: Michael Silverberg, MD Beth Israel Medical Center
Beth Israel Medical Center
October 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP