Assisted Intubation

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Thomas Hemmerling, McGill University Health Center
ClinicalTrials.gov Identifier:
NCT01312155
First received: March 8, 2011
Last updated: October 24, 2013
Last verified: October 2013
  Purpose

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 ] [ Designated as safety issue: No ]
    Success rate in % of intubation: Number of patients where 'assisted intubation' was successful


Secondary Outcome Measures:
  • Time [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    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

  Eligibility

Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients undergoing general anesthesia with endotracheal intubation

Criteria

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 ClinicalTrials.gov identifier: NCT01312155

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

No publications provided

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

Keywords provided by McGill University Health Center:
endotracheal
intubation
video
time

ClinicalTrials.gov processed this record on July 22, 2014