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OpenTrials
Completed

NCT Number: NCT00833118

Tongue Pull Versus Jaw Thrust

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Mayo Clinic Florida

Jacksonville, Florida, 32224, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 18
  • Undergoing surgery and general anesthesia with endotracheal intubation
  • Able to give informed consent

Exclusion criteria

  • Trauma patients or emergent cases.
  • Patients who are unable to understand the proposed study
  • Patients who refuse participation

Treatment and study plan

Jaw thrust maneuver (Intubation)

Procedure

Visualization of Larygnoscopic anatomy during intubation

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jan 30, 2009
Registry last updated
Feb 12, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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