Try our beta test site
IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more...

Assisted Intubation

This study has been completed.
Information provided by (Responsible Party):
Thomas Hemmerling, McGill University Health Center Identifier:
First received: March 8, 2011
Last updated: October 24, 2013
Last verified: October 2013
The study investigates assisted intubation using a videolaryngoscope in anesthesia.

Condition Intervention
Intubation Conditions
Other: Intubation

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective

Further study details as provided by McGill University Health Center:

Primary Outcome Measures:
  • Performance [ Time Frame: 3 months ]
    Success rate in % of intubation: Number of patients where 'assisted intubation' was successful

Secondary Outcome Measures:
  • Time [ Time Frame: 3 months ]
    Time to intubate: time in sec between insertion of scope into mouth and insertion of endotracheal tube through vocal cords

Enrollment: 12
Study Start Date: March 2011
Study Completion Date: February 2012
Primary Completion Date: February 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Patients undergoing general anesthesia Other: Intubation
Intubation, endotracheal


Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients undergoing general anesthesia with endotracheal intubation

Inclusion Criteria:

  • Easy airway assessment

Exclusion Criteria:

  • Difficult airway
  • ASA 3
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01312155

Canada, Quebec
Montreal, Quebec, Canada, H3G1A4
Sponsors and Collaborators
McGill University Health Center
Principal Investigator: Thomas Hemmerling, MD MUHC - McGill
  More Information

Responsible Party: Thomas Hemmerling, Associate Professor, McGill University Health Center Identifier: NCT01312155     History of Changes
Other Study ID Numbers: 10-338
Study First Received: March 8, 2011
Last Updated: October 24, 2013

Keywords provided by McGill University Health Center:
time processed this record on May 25, 2017