Skip to main content
Clinical Trials/NCT00917033
NCT00917033
Completed
Phase 4

Orotracheal Intubation of Morbidly Obese Patients. A Randomised Controlled Trial Comparing the GlideScope Videolaryngoscope to the Macintosh Direct Laryngoscope.

Glostrup University Hospital, Copenhagen1 site in 1 country100 target enrollmentSeptember 2008

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Intubation, Endotracheal
Sponsor
Glostrup University Hospital, Copenhagen
Enrollment
100
Locations
1
Primary Endpoint
Time to intubate
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The purpose of this study is to examine whether orotracheal intubation in morbidly obese patients is faster, gentler and safer using the GlideScope videolaryngoscope than with the Macintosh direct laryngoscope.

Registry
clinicaltrials.gov
Start Date
September 2008
End Date
October 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Glostrup University Hospital, Copenhagen

Eligibility Criteria

Inclusion Criteria

  • Approved for elective bariatric surgery at Glostrup University Hospital, Copenhagen.
  • Body Mass Index at least 35 kg/m2
  • Written informed consent to participate

Exclusion Criteria

  • Mental illness
  • Abuse of alcohol or other substances
  • Previous difficult tracheal intubation
  • Considered non-eligible for safety-reasons by the anesthetist in charge

Outcomes

Primary Outcomes

Time to intubate

Time Frame: Measured during intubation (seconds)

Secondary Outcomes

  • Number of intubation attempts(Measured during intubation (seconds))
  • Lowest arterial oxygen saturation during intubation(Measured during intubation (seconds))
  • Subjective difficulty of intubation(Measured during intubation (seconds))
  • Cormack-Lehane Score(Measured during intubation (seconds))
  • Airway mucosal trauma(Measured during intubation (seconds))
  • Dental injury(Measured during intubation (seconds))
  • Post-procedure sore throat(One hour post-operative)
  • Post-procedure hoarseness of voice(One hour post-operative)

Study Sites (1)

Loading locations...

Similar Trials