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Assisted Intubation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01312155
First Posted: March 10, 2011
Last Update Posted: October 25, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Thomas Hemmerling, McGill University Health Center
  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 Thomas Hemmerling, 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

  Eligibility

Information from the National Library of Medicine

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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
Criteria

Inclusion Criteria:

  • Easy airway assessment

Exclusion Criteria:

  • Difficult airway
  • ASA 3
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Thomas Hemmerling, Associate Professor, McGill University Health Center
ClinicalTrials.gov Identifier: NCT01312155     History of Changes
Other Study ID Numbers: 10-338
First Submitted: March 8, 2011
First Posted: March 10, 2011
Last Update Posted: October 25, 2013
Last Verified: October 2013

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