Identification of Morphological Characteristics to Predict Difficult Endotracheal Intubation Using a Flexible Fiberscope

Overview

This study is designed to identify patients' features predictive of difficult endotracheal intubation using a flexible fiberscope.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Other
    • Masking: None (Open Label)
  • Study Primary Completion Date: September 12, 2017

Detailed Description

Endotracheal intubation is an important act in the practice of anesthesiology. Direct laryngoscopy is the most commonly used technique to accomplish this task. Airway characteristics predicting difficult intubation with direct laryngoscopy are well defined. Physical findings, such as Mallampati classification or measurements of the thyromental distance, mouth opening, and neck extension have been validated to help anticipate difficult situations with the direct laryngoscope. When direct laryngoscopy is difficult, early conversion to an alternative technique reduces the risk of airway compromise and associated morbidity. Many alternative intubation devices are now available, and part of the anesthesiologist's task is to select the alternative approach best suited to each patient's specific features. Despite its use for both elective and unexpectedly difficult intubation, predictive criteria for successful airway management with the flexible fiberscope have not been developed. The purpose of this study is to identify patient morphometric or morphological characteristics, if any, that could predict difficult intubation when using the flexible fiberscope for perioperative tracheal intubation in an elective surgical population.

Interventions

  • Device: Flexible fiberscope
    • Characteristics of patients will be assessed before induction of general anesthesia Glottic visualization will be evaluated by direct laryngoscopy. The endotracheal tube will be loaded onto the scope after silicon spray lubrication Intubation will be performed with the flexible fiberscope with the patient in supine position with head and neck in neutral position With the tip of the fiberscope in satisfactory position, the endotracheal tube will be advanced into the trachea. The scope will then be removed. Accurate positioning of the endotracheal tube will be confirmed by capnography and lung auscultation.

Arms, Groups and Cohorts

  • Experimental: Intubation with a flexible fiberscope
    • Following induction of general anesthesia and administration of a neuromuscular blocking agent, intubation will be performed using a flexible fiberscope.

Clinical Trial Outcome Measures

Primary Measures

  • Morphologic and morphometric predictors of difficult intubation with the flexible fiberscope.
    • Time Frame: Patients will be followed from induction of anesthesia until the end of intubation, an average of 10 minutes
    • This study will correlate patients’ morphometric and morphologic characteristics with the number of attempts and time needed for intubation using a flexible fiberscope.

Secondary Measures

  • Time to successful intubation
    • Time Frame: Patients will be followed from induction of anesthesia until the end of intubation, an average of 10 minutes
  • Number of attempts to successful intubation
    • Time Frame: Patients will be followed from induction of anesthesia until the end of intubation, an average of 10 minutes
  • Score on the Intubation Difficulty Scale
    • Time Frame: Patients will be followed from induction of anesthesia until the end of intubation, an average of 10 minutes
    • To calculate the Intubation Difficulty Scale the following variables will be collected: number of attempts, number of operators, necessity to use an alternative intubation technique, glottic visualization and effort needed to obtain optimal view of the glottis, necessity of external laryngeal pressure and vocal cords position during intubation.

Participating in This Clinical Trial

Inclusion Criteria

  • Age 18 and older – Patients undergoing elective surgery under general anesthesia, requiring endotracheal intubation Exclusion Criteria:

  • Induction planned without neuromuscular blocking agents – Need for a rapid sequence induction

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Centre hospitalier de l’Université de Montréal (CHUM)
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Stephan R Williams, MD, PhD, Principal Investigator, Centre hospitalier de l’Université de Montréal (CHUM)

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