Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Beth Israel Medical Center
ClinicalTrials.gov Identifier:
NCT01683526
First received: September 6, 2012
Last updated: May 23, 2014
Last verified: May 2014

September 6, 2012
May 23, 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 ] [ Designated as safety issue: Yes ]
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 ] [ Designated as safety issue: Yes ]
    sat <80%
  • Hypotension [ Time Frame: For 10 minutes post intubation ] [ Designated as safety issue: Yes ]
    SBP<70
  • Cardiac Arrest [ Time Frame: For 1 hour post intubation ] [ Designated as safety issue: Yes ]
  • Complications of Intubation [ Time Frame: For 10 minutes post intubation ] [ Designated as safety issue: Yes ]
    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
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: 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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01683526
139-12
No
Beth Israel Medical Center
Beth Israel Medical Center
Not Provided
Not Provided
Beth Israel Medical Center
May 2014

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