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Clinical Trials/NCT02884869
NCT02884869
Unknown
Not Applicable

Establishing a Definitive Airway: Comparison of Direct Laryngoscopy With Blind Intubation Via Intubating Laryngeal Mask Airway

Bnai Zion Medical Center0 sites60 target enrollmentAugust 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adverse Anesthesia Outcome
Sponsor
Bnai Zion Medical Center
Enrollment
60
Primary Endpoint
Time of blind intubation measure in second
Last Updated
9 years ago

Overview

Brief Summary

Control the airways by endotracheal intubation is an important part of treatment for a trauma casualty. The use of the Laryngeal Mask Airway for fast control of the airway is known for many years. The aim of this study is to examine the effectiveness of the Intubating Laryngeal Mask Airway to achieve a definitive airway by unskilled practitioners.

The hypothesis is that definitive airway obtaining with Intubating Laryngeal Mask Airway will be more success and faster compared to the standard way of direct laryngoscope.

Detailed Description

Control the airways and respiration are an important part of treatment for a trauma casualty. Tracheal intubation an action that allows the insertion of a tube through the vocal cords and fixation by the balloon inflation is a definitive airway. The use of the Laryngeal Mask Airway for fast control of the airway is known for many years. The Laryngeal Mask Airway and others similar devices are known as Supraglottic Airway Devices and are inserted blind in the oropharynx and allow a fast oxygenation and ventilation of the patients.The aim of this study is to examine the effectiveness of the Laryngeal Mask Airway to achieve a definitive airway by unskilled practitioners in anesthetized patients with the head in neutral position (trauma model) The hypothesis is that definitive airway obtaining with Intubating Laryngeal Mask Airway will be more success and faster compared to the standard way of direct laryngoscope. If the hypothesis is proven, this research will be very important implications for the management of the airway describing pre-hospital and in particular military scenarios.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
September 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

LUIS.GAITINI

M.D.

Bnai Zion Medical Center

Eligibility Criteria

Inclusion Criteria

  • American Society Anesthesiology class I and II

Exclusion Criteria

  • Difficult airway
  • Cervical pathology
  • Full stomach

Outcomes

Primary Outcomes

Time of blind intubation measure in second

Time Frame: 30 seconds

Time of blind intubation in seconds

Secondary Outcomes

  • Easy to perform intubation measure in numeric scale(30 seconds)

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