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Bougie Use in Emergency Airway Management (BEAM)

Primary Purpose

Acute Respiratory Failure

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bougie
Endotracheal tube
Sponsored by
Hennepin Healthcare Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Failure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. The patient must be undergoing orotracheal intubation in the ED with a Macintosh blade (using either video or direct laryngoscopy)
  2. The patient must be presumed to be 18 years of age or older at the time of enrollment.

Exclusion Criteria:

  1. Known anatomic distortion of the upper airway or perilaryngeal structures.
  2. Prisoner or under arrest
  3. Known or suspected to be pregnant, based on the opinion of the treating physician.

Sites / Locations

  • Hennepin County Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Bougie

No bougie (endotracheal tube first)

Arm Description

On the first intubation attempt, this arm will attempt to place a bougie into the trachea, followed by an endotracheal tube.

On the first intubation attempt, this arm will attempt to place an endotracheal tube into the trachea directly.

Outcomes

Primary Outcome Measures

Number of Participants With First Pass Success
First pass success is defined as placement of the endotracheal tube (ETT) into the trachea on the first attempt. An attempt begins when the laryngoscope enters the mouth, and ends if either of the following occur: the laryngoscope leaves the mouth, regardless of whether an attempt was made to pass the endotracheal tube or bougie. if the operator cannot intubate the trachea with the first tube device (ETT or bougie), and switches to any other tube device, even if the laryngoscope blade remains in the mouth. A patient will be considered to achieve the primary outcome if they are intubated successfully on the first attempt.

Secondary Outcome Measures

First Pass Success Without Hypoxemia
First pass success without hypoxemia. Hypoxemia is defined as a pulse oximetry value (SpO2) less than 90% at any point during intubation, or a drop of more than 10% from baseline if starting below 90%. The outcome of hypoxemia will be recorded beginning when the first attempt begins and ending one minute after inflation of the ETT cuff. A patient will be considered to achieve this outcome if 1) they are intubated successfully on the first attempt, and 2) do not experience hypoxemia on the first attempt.
Time to Intubation (First Attempt)
Time to intubation will be defined as the time elapsed between the beginning of the intubation attempt to inflation of the ETT cuff when the tube is in the trachea.
Esophageal Intubation
defined as passage of the ETT into the esophagus, with subsequent ventilation, and then removal. Clinically, esophageal intubation is identified by the absence of end-tidal carbon dioxide, abnormal physical exam, and hypoxia. This does not count passage of the ETT into the esophagus during the attempt if the ETT is removed during the attempt.
Hypoxemia
Hypoxemia is defined as a pulse oximetry value (SpO2) less than 90% at any point during intubation, or a drop of more than 10% from baseline if starting below 90%. The outcome of hypoxemia will be recorded beginning when the first attempt begins and ending one minute after inflation of the ETT cuff.

Full Information

First Posted
September 12, 2016
Last Updated
May 21, 2019
Sponsor
Hennepin Healthcare Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02902146
Brief Title
Bougie Use in Emergency Airway Management
Acronym
BEAM
Official Title
Bougie Use in Emergency Airway Management
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
September 27, 2016 (Actual)
Primary Completion Date
August 20, 2017 (Actual)
Study Completion Date
August 20, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hennepin Healthcare Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This prospective, open-label trial randomizes adult patients intubated in the ED with a Macintosh blade to use or not use a bougie for the first intubation attempt. The primary outcome is first pass success.
Detailed Description
The primary analysis for all outcomes will be for those with a difficult airway characteristic (defined as any of: cervical immobility, obesity, large tongue, short neck, small mandible, facial or neck trauma, airway edema, blood in the airway, or vomit in the airway). We will also analyze all outcomes for all patients enrolled, regardless of whether they have a difficult airway characteristic. We plan to enroll 374 patients with a difficult airway characteristic (DAC). The total enrollment for the trial will be higher, depending on the proportion of patients that have a DAC. Based on observational data, we aim to detect a 9% absolute difference in first pass success (95% with bougie compared to 86% without the bougie), which requires enrollment of 374 patients with a DAC. To help achieve balanced randomization for patients with a DAC, patients are stratified into two groups: 1) obese or cervical immobilization present and 2) not obese and no cervical immobilization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
757 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bougie
Arm Type
Active Comparator
Arm Description
On the first intubation attempt, this arm will attempt to place a bougie into the trachea, followed by an endotracheal tube.
Arm Title
No bougie (endotracheal tube first)
Arm Type
Active Comparator
Arm Description
On the first intubation attempt, this arm will attempt to place an endotracheal tube into the trachea directly.
Intervention Type
Device
Intervention Name(s)
Bougie
Intervention Type
Device
Intervention Name(s)
Endotracheal tube
Primary Outcome Measure Information:
Title
Number of Participants With First Pass Success
Description
First pass success is defined as placement of the endotracheal tube (ETT) into the trachea on the first attempt. An attempt begins when the laryngoscope enters the mouth, and ends if either of the following occur: the laryngoscope leaves the mouth, regardless of whether an attempt was made to pass the endotracheal tube or bougie. if the operator cannot intubate the trachea with the first tube device (ETT or bougie), and switches to any other tube device, even if the laryngoscope blade remains in the mouth. A patient will be considered to achieve the primary outcome if they are intubated successfully on the first attempt.
Time Frame
5 minutes
Secondary Outcome Measure Information:
Title
First Pass Success Without Hypoxemia
Description
First pass success without hypoxemia. Hypoxemia is defined as a pulse oximetry value (SpO2) less than 90% at any point during intubation, or a drop of more than 10% from baseline if starting below 90%. The outcome of hypoxemia will be recorded beginning when the first attempt begins and ending one minute after inflation of the ETT cuff. A patient will be considered to achieve this outcome if 1) they are intubated successfully on the first attempt, and 2) do not experience hypoxemia on the first attempt.
Time Frame
5 minutes
Title
Time to Intubation (First Attempt)
Description
Time to intubation will be defined as the time elapsed between the beginning of the intubation attempt to inflation of the ETT cuff when the tube is in the trachea.
Time Frame
5 minutes
Title
Esophageal Intubation
Description
defined as passage of the ETT into the esophagus, with subsequent ventilation, and then removal. Clinically, esophageal intubation is identified by the absence of end-tidal carbon dioxide, abnormal physical exam, and hypoxia. This does not count passage of the ETT into the esophagus during the attempt if the ETT is removed during the attempt.
Time Frame
5 minutes
Title
Hypoxemia
Description
Hypoxemia is defined as a pulse oximetry value (SpO2) less than 90% at any point during intubation, or a drop of more than 10% from baseline if starting below 90%. The outcome of hypoxemia will be recorded beginning when the first attempt begins and ending one minute after inflation of the ETT cuff.
Time Frame
5 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient must be undergoing orotracheal intubation in the ED with a Macintosh blade (using either video or direct laryngoscopy) The patient must be presumed to be 18 years of age or older at the time of enrollment. Exclusion Criteria: Known anatomic distortion of the upper airway or perilaryngeal structures. Prisoner or under arrest Known or suspected to be pregnant, based on the opinion of the treating physician.
Facility Information:
Facility Name
Hennepin County Medical Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55415
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
29800096
Citation
Driver BE, Prekker ME, Klein LR, Reardon RF, Miner JR, Fagerstrom ET, Cleghorn MR, McGill JW, Cole JB. Effect of Use of a Bougie vs Endotracheal Tube and Stylet on First-Attempt Intubation Success Among Patients With Difficult Airways Undergoing Emergency Intubation: A Randomized Clinical Trial. JAMA. 2018 Jun 5;319(21):2179-2189. doi: 10.1001/jama.2018.6496.
Results Reference
derived

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Bougie Use in Emergency Airway Management

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