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Assisted Intubation

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.
ClinicalTrials.gov Identifier: NCT01312155
Recruitment Status : Completed
First Posted : March 10, 2011
Last Update Posted : October 25, 2013
Information provided by (Responsible Party):

Study Description
Brief Summary:
The study investigates assisted intubation using a videolaryngoscope in anesthesia.

Condition or disease Intervention/treatment
Intubation Conditions Other: Intubation

Study Design

Study Type : Observational
Actual Enrollment : 12 participants
Observational Model: Case Control
Time Perspective: Prospective
Study Start Date : March 2011
Primary Completion Date : February 2012
Study Completion Date : February 2012
Groups and Cohorts

Group/Cohort Intervention/treatment
Patients undergoing general anesthesia Other: Intubation
Intubation, endotracheal

Outcome Measures

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

Secondary Outcome Measures :
  1. 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

Eligibility Criteria

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

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

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
ClinicalTrials.gov Identifier: NCT01312155     History of Changes
Other Study ID Numbers: 10-338
First Posted: March 10, 2011    Key Record Dates
Last Update Posted: October 25, 2013
Last Verified: October 2013

Keywords provided by Thomas Hemmerling, McGill University Health Center: