Recruiting

Videolaryngoscope vs. Fiberoptic Bronchoscope

Sponsor:

McGill University Health Centre/Research Institute of the McGill University Health Centre

Code:

NCT02169232

Conditions

Need of Awake Intubation for Difficult Airways

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Not accepted

Interventions

Videolaryngoscope

Fiberoptic

Study Details

Brief summary:

Endotracheal intubation of the morbidly obese is often performed awake. Fiberoptic bronchoscope assisted endotracheal intubation, a commonly utilized technique for securing an airway while a patient is awake, has many limitations. The video laryngoscope is a device that is similar to a conventional laryngoscope but uses a video system to visualize the larynx. Because of its low cost, ease of use, and usefulness in the presence of edema or bleeding that may obstruct the airway, video assisted laryngoscopy has been shown to be useful for awake endotracheal intubations. However, a direct comparison of the fiberoptic bronchoscope with video assisted laryngoscopy has not been performed for awake endotracheal intubations in of obese patients. Patients undergoing laparoscopic gastric bypas andrecquiring awake intubations will be randomized for either fiberoptic bronchoscope or video assisted laryngoscopy. The investigators primary outcome will be the time required for successful intubation.

Conditions

Need of Awake Intubation for Difficult Airways

Study ID

NCT02169232

Start date

May, 2014

Status verified date

Jun, 2014

Completion date

Dec, 2015

Anticipated

Primary completion date

May, 2015

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • morbidly obese patient presenting for bariatric surgery at the Royal Victoria Hospital

Exclusion Criteria:

  • moderate to severe systemic illness, i.e. American Society of Anesthesiologists (ASA) score of 4 or higher
  • inability to communicate in English or French
  • contraindications to the drugs used in the study

Study Design

Enrollment

40 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

active comparator: Videolaryngoscope

Intubation by videolaryngoscope

active comparator: Fiberoptic

Intubation by fibroscope

Interventions

Videolaryngoscope

Fiberoptic

Primary outcome measure

  • The time required for successful intubation [ Time Frame: 10 minutes ]

Central Contacts and Locations

Central contacts

Albert Moore, MD

moore_albert@hotmail.com

Aly Elbahrawy, MD

abahrawy@yahoo.com

Locations

Royal Victoria Hospital

Recruiting

Montreal, Quebec, Canada

Contacts

Albert Moore, MD

moore_albert@hotmail.com

More Information

Sponsor

McGill University Health Centre/Research Institute of the McGill University Health Centre

Last update posted

Jun 23, 2014

Last verified

Jun, 2014

Keywords

  • Awake intubation
  • Videolaryngoscope
  • Fiberoptic

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by McGill University Health Centre/Research Institute of the McGill University Health Centre on 2014-06-23.