Assisted Intubation

This study is currently recruiting participants.
Verified June 2011 by McGill University Health Center
Sponsor:
Information provided by:
McGill University Health Center
ClinicalTrials.gov Identifier:
NCT01312155
First received: March 8, 2011
Last updated: June 8, 2011
Last verified: June 2011
  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


Estimated Enrollment: 20
Study Start Date: March 2011
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: December 2011 (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
Please refer to this study by its ClinicalTrials.gov identifier: NCT01312155

Contacts
Contact: Thomas Hemmerling, MD 5149341934 ext 43677 thomas.hemmerling@mcgill.ca

Locations
Canada, Quebec
MUHC Recruiting
Montreal, Quebec, Canada, H3G1A4
Contact: Thomas Hemmerling, MD     514-934-1934 ext 43677     thomas.hemmerling@mcgill.ca    
Principal Investigator: Thomas Hemmerling, MD            
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, MUHC
ClinicalTrials.gov Identifier: NCT01312155     History of Changes
Other Study ID Numbers: 10-338
Study First Received: March 8, 2011
Last Updated: June 8, 2011
Health Authority: Canada: Ethics Review Committee

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

ClinicalTrials.gov processed this record on May 23, 2013