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Tongue Pull Versus Jaw Thrust

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00833118
First Posted: January 30, 2009
Last Update Posted: February 12, 2010
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:
Mayo Clinic
  Purpose
This protocol seeks to determine the efficacy and reliability of a simple maneuver, the jaw thrust maneuver, in addition to cricoid pressure, in improving visualization of airway anatomy during video laryngoscopy. Hypothesis: The grade of view of the glottis as determined by the modified Cormack and Lehane grading system in anesthetized patients will improve by performing a jaw thrust maneuver during video laryngoscopy with compared with video laryngoscopy alone. Similarly, the grade of the view during cricoid pressure will also improve with a jaw thrust maneuver.

Condition Intervention
Surgery Procedure: Jaw thrust maneuver (Intubation)

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Tongue Pull Versus Jaw Thrust

Further study details as provided by Mayo Clinic:

Enrollment: 100
Study Start Date: November 2008
Study Completion Date: February 2010
Primary Completion Date: February 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Intubation Procedure: Jaw thrust maneuver (Intubation)
Visualization of Larygnoscopic anatomy during intubation

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Male or female scheduled for surgery and undergoing intubation for general anesthesia administration
Criteria

Inclusion Criteria:

  1. Age > 18
  2. Undergoing surgery and general anesthesia with endotracheal intubation
  3. Able to give informed consent

Exclusion Criteria:

  1. Trauma patients or emergent cases.
  2. Patients who are unable to understand the proposed study
  3. Patients who refuse participation
  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): NCT00833118


Locations
United States, Florida
Mayo Clinic Florida
Jacksonville, Florida, United States, 32224
Sponsors and Collaborators
Mayo Clinic
Investigators
Principal Investigator: Sorin Brull, M.D. Mayo Clinic
  More Information

Responsible Party: Sorin Brull, M.D., Mayo Clinic Florida
ClinicalTrials.gov Identifier: NCT00833118     History of Changes
Other Study ID Numbers: 07-004837
First Submitted: January 29, 2009
First Posted: January 30, 2009
Last Update Posted: February 12, 2010
Last Verified: February 2010

Keywords provided by Mayo Clinic:
Surgery
General Anesthesia
Intubation