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DirEct Versus VIdeo LaryngosCopE Trial

DirEct Versus VIdeo LaryngosCopE Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05239195
Acronym
DEVICE
Enrollment
1420
Registered
2022-02-14
Start date
2022-03-19
Completion date
2022-12-16
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Failure

Keywords

Critical Illness, Emergency Airway Management, Tracheal intubation, Video laryngoscope, Direct laryngoscope

Brief summary

Clinicians perform rapid sequence induction, laryngoscopy, and tracheal intubation for more than 5 million critically ill adults as a part of clinical care each year in the United States. Failure to intubate the trachea on the first attempt occurs in more than 10% of all tracheal intubation procedures performed in the emergency department (ED) and intensive care unit (ICU). Improving clinicians rate of intubation on the first attempt could reduce the risk of serious procedural complications. In current clinical practice, two classes of laryngoscopes are commonly used to help clinicians view the larynx while intubating the trachea: a video laryngoscope (equipped with a camera and a video screen) and a direct laryngoscope (not equipped with a camera or video screen). For nearly all laryngoscopy and intubation procedures performed in current clinical practice, clinicians use either a video or a direct laryngoscope. Prior research has shown that use of a video laryngoscope improves the operator's view of the larynx compared to a direct laryngoscope. Whether use of a video laryngoscope increases the likelihood of successful intubation on the first attempt remains uncertain. A better understanding of the comparative effectiveness of these two common, standard-of-care approaches to laryngoscopy and intubation could improve the care clinicians deliver and patient outcomes.

Detailed description

Clinicians frequently perform tracheal intubation of critically ill patients in the emergency department (ED) or intensive care unit (ICU). In 10-20% of emergency tracheal intubations, clinicians are unable to intubate the trachea on the first attempt, which increases the risk of peri-intubation complications. Successful laryngoscopy and tracheal intubation requires using a laryngoscope to \[1\] visualize the larynx and vocal cords and \[2\] create a pathway through which an endotracheal tube can be advanced through the oropharynx and larynx and into the trachea. In current clinical practice, two classes of laryngoscopes are commonly used by clinicians to view the larynx while intubating the trachea: a video laryngoscope (equipped with a camera and a video screen) and a direct laryngoscope (not equipped with a camera or video screen). Clinicians use either a video laryngoscope or a direct laryngoscope as standard of care for every laryngoscopy and intubation procedure performed in current clinical practice. Direct Laryngoscope: The Macintosh direct laryngoscope consists of a battery-containing handle and a blade with a light source. The operator achieves a direct line of sight -from the operator's eye through the mouth to the larynx and trachea - by using the laryngoscope blade to displace the tongue and elevate the epiglottis. Video Laryngoscope: Video laryngoscopes consist of a fiberoptic camera and light source near the tip of the laryngoscope blade, which transmits images to a video screen. The position of the camera near the tip of the laryngoscope blade facilitates visualization of the larynx and trachea. Use of a video laryngoscope and use of a direct laryngoscope are both common, standard-of-care approaches the clinicians use to perform tracheal intubation in the ED and ICU in current clinical care. Currently, it is unknown whether use of a video laryngoscope or use of a direct laryngoscope has any effect on successful intubation on the first attempt or any other outcome. Some prior research has raised the hypothesis that using a video laryngoscope would increase clinicians' rate of successful intubation on the first attempt by facilitating the view of the larynx. Some prior research has raised the hypothesis that using a direct laryngoscope would increase clinicians' rate of successful intubation on the first attempt by facilitating a clear pathway for placement of the tube through the mouth into the trachea. To date, 8 small single-center randomized trials and one 371-patient multicenter randomized clinical trial have been conducted under waiver of or alteration of informed consent to compare use of a video vs a direct laryngoscope in the setting of emergency tracheal intubation in the ED or ICU. Two of these trials provide the most direct preliminary data for this proposal. The Facilitating EndotracheaL intubation by Laryngoscopy technique and apneic Oxygenation Within the ICU (FELLOW) randomized clinical trial, conducted under waiver of informed consent, compared these two standard-of-care approaches during 150 emergency tracheal intubations at Vanderbilt University Medical Center, finding no difference in the rate of successful intubation on the first attempt between use of a video and use of a direct laryngoscope. The McGrath Mac Videolaryngoscope Versus Macintosh Laryngoscope for Orotracheal Intubation in the Critical Care Unit (MACMAN) randomized clinical trial among 371 critically ill adults found no difference between use of a video vs direct laryngoscope in the rate of successful intubation on the first attempt. However, a hypothesis-forming post-hoc exploratory analysis of peri-intubation complications suggested that use of a video laryngoscope may be associated with a higher rate of complications than direct laryngoscope (9.5% vs 2.8%, respectively, p=0.01). These trials were underpowered to rule out small but clinically significant differences in first pass success, and were limited to intubations performed by inexperienced trainees in one practice setting (intensive care units), but they demonstrated hypothesis-generating findings requiring validation in larger trials that reflect the full spectrum of settings, operator specialties, and operator experience levels in which emergency tracheal intubation is routinely performed. Because of the imperative to optimize emergency tracheal intubation in clinical care, the common use of both video and direct laryngoscopes in current clinical practice, and the lack of definitive data from randomized trials to definitively inform whether use of a video laryngoscope or a direct laryngoscope effects the rate of successful intubation on the first attempt, examining whether one approach increases the odds of successful intubation on the first attempt represents an urgent research priority. To address this knowledge gap, the investigators propose to conduct a large, multicenter, randomized clinical trial comparing use of a video laryngoscope versus use of a direct laryngoscope with regard to successful intubation on the first attempt among critically ill adults undergoing tracheal intubation in the ED or ICU.

Interventions

Laryngoscope with a camera and a video screen

Laryngoscope without a camera or a video screen

Sponsors

University of Colorado, Denver
CollaboratorOTHER
Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient is located in a participating unit. * Planned procedure is orotracheal intubation using a laryngoscope. * Planned operator is a clinician expected to routinely perform tracheal intubation in the participating unit.

Exclusion criteria

* Patient is known to be less than 18 years old. * Patient is known to be pregnant. * Patient is known to be a prisoner. * Immediate need for tracheal intubation precludes safe performance of study procedures. * Operator has determined that use of a video laryngoscope or use of a direct laryngoscope is required or contraindicated for the optimal care of the patient.

Design outcomes

Primary

MeasureTime frameDescription
Number of Intubations With Successful Intubation on the First AttemptDuration of procedure (minutes)The primary outcome is defined as placement of an endotracheal tube in the trachea with a single insertion of a laryngoscope blade into the mouth and EITHER a single insertion of an endotracheal tube into the mouth OR a single insertion of a bougie into the mouth followed by a single insertion of an endotracheal tube over the bougie into the mouth.

Secondary

MeasureTime frameDescription
Number of Participants With Severe Complications of Tracheal Intubationfrom induction to 2 minutes following tracheal intubationThe secondary outcome is defined as the number of patients who experienced one or more of the following occurring between induction and 2 minutes after successful intubation: * Severe hypoxemia (lowest oxygen saturation measured by pulse oximetry \< 80%); * Severe hypotension (systolic blood pressure \< 65 mm Hg or new or increased vasopressor administration); * Cardiac arrest not resulting in death within 1 hour of intubation; or * Cardiac arrest resulting in death within 1 hour of induction

Other

MeasureTime frameDescription
Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeDuration of procedure (minutes)
Successful Intubation on the First Attempt Without a Severe Complicationfrom induction to 2 minutes following tracheal intubationThis outcome reports the number of participants that experienced successful intubation on the first attempt without experiencing complications, a composite of two independent outcomes: successful intubation on the first attempt (the primary outcome of the trial) and severe complication (the secondary outcome of the trial).
Reason for Failure to Intubate on the First AttemptDuration of procedure (minutes)Providers could give more than one reason for failure to intubate on the first attempt for each intubation (not mutually exclusive). In addition, data on the reason for failure to intubate on the first attempt was missing for 23 patients in the video laryngoscope group and 40 patients in the direct laryngoscope group. Reason for failure among those who did not meet the primary outcome (successful intubation on the first attempt): * Inadequate view of the larynx * Inability to intubate the trachea with an endotracheal tube * Inability to cannulate the trachea with a bougie * Attempt aborted due to change in patient condition (e.g., worsening hypoxemia, hypotension, bradycardia, vomiting, bleeding) * Technical failure of the laryngoscope (e.g., battery, light source, camera, screen) * Other * Not Reported
Operator-reported Aspirationfrom induction to 2 minutes following tracheal intubation
Duration of Laryngoscopy and Tracheal IntubationDuration of procedure (minutes)The interval (in seconds) between the first insertion of a laryngoscope blade into the mouth and the final placement of an endotracheal tube or tracheostomy tube in the trachea.
Injury to the Teethfrom induction to 2 minutes following tracheal intubation
ICU-free Days in the First 28 Days28 days
Ventilator Free Days in the First 28 Days28 days
All-cause In-hospital Mortality28 days
Esophageal Intubationfrom induction to 2 minutes following tracheal intubation
Number of Laryngoscopy AttemptsDuration of procedure (minutes)

Countries

United States

Participant flow

Participants by arm

ArmCount
Video Laryngoscope Group
For patients assigned to the video laryngoscope group, the operator will use a video laryngoscope on the first laryngoscopy attempt. A video laryngoscope will be defined as a laryngoscope with a camera and a video screen. Trial protocol will not dictate the brand of video laryngoscope. Video Laryngoscope: Laryngoscope with a camera and a video screen
705
Direct Laryngoscope Group
For patients assigned to the direct laryngoscope group, the operator will use a direct laryngoscope on the first laryngoscopy attempt. A direct laryngoscope will be defined as a laryngoscope without a camera or a video screen. Trial protocol will not dictate the brand of direct laryngoscope or the blade shape. Direct Laryngoscope: Laryngoscope without a camera or a video screen
712
Total1,417

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAfter enrollment, discovered to be a person experiencing incarceration.21

Baseline characteristics

CharacteristicVideo Laryngoscope GroupDirect Laryngoscope GroupTotal
Age, Continuous54 years55 years55 years
Race/Ethnicity, Customized
Race or ethnic group
Hispanic
101 Participants94 Participants195 Participants
Race/Ethnicity, Customized
Race or ethnic group
Non-Hispanic Black
166 Participants167 Participants333 Participants
Race/Ethnicity, Customized
Race or ethnic group
Non-Hispanic White
360 Participants346 Participants706 Participants
Race/Ethnicity, Customized
Race or ethnic group
Not reported
17 Participants21 Participants38 Participants
Race/Ethnicity, Customized
Race or ethnic group
Other
61 Participants84 Participants145 Participants
Region of Enrollment
United States
705 participants712 participants1417 participants
Sex: Female, Male
Female
240 Participants258 Participants498 Participants
Sex: Female, Male
Male
465 Participants454 Participants919 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
184 / 705191 / 712
other
Total, other adverse events
0 / 7050 / 712
serious
Total, serious adverse events
0 / 7050 / 712

Outcome results

Primary

Number of Intubations With Successful Intubation on the First Attempt

The primary outcome is defined as placement of an endotracheal tube in the trachea with a single insertion of a laryngoscope blade into the mouth and EITHER a single insertion of an endotracheal tube into the mouth OR a single insertion of a bougie into the mouth followed by a single insertion of an endotracheal tube over the bougie into the mouth.

Time frame: Duration of procedure (minutes)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupNumber of Intubations With Successful Intubation on the First Attempt600 Participants
Direct Laryngoscope GroupNumber of Intubations With Successful Intubation on the First Attempt504 Participants
Secondary

Number of Participants With Severe Complications of Tracheal Intubation

The secondary outcome is defined as the number of patients who experienced one or more of the following occurring between induction and 2 minutes after successful intubation: * Severe hypoxemia (lowest oxygen saturation measured by pulse oximetry \< 80%); * Severe hypotension (systolic blood pressure \< 65 mm Hg or new or increased vasopressor administration); * Cardiac arrest not resulting in death within 1 hour of intubation; or * Cardiac arrest resulting in death within 1 hour of induction

Time frame: from induction to 2 minutes following tracheal intubation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupNumber of Participants With Severe Complications of Tracheal Intubation151 Participants
Direct Laryngoscope GroupNumber of Participants With Severe Complications of Tracheal Intubation149 Participants
Other Pre-specified

All-cause In-hospital Mortality

Time frame: 28 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupAll-cause In-hospital Mortality184 Participants
Direct Laryngoscope GroupAll-cause In-hospital Mortality191 Participants
Other Pre-specified

Duration of Laryngoscopy and Tracheal Intubation

The interval (in seconds) between the first insertion of a laryngoscope blade into the mouth and the final placement of an endotracheal tube or tracheostomy tube in the trachea.

Time frame: Duration of procedure (minutes)

ArmMeasureValue (MEDIAN)
Video Laryngoscope GroupDuration of Laryngoscopy and Tracheal Intubation38 Seconds
Direct Laryngoscope GroupDuration of Laryngoscopy and Tracheal Intubation46 Seconds
Other Pre-specified

Esophageal Intubation

Time frame: from induction to 2 minutes following tracheal intubation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupEsophageal Intubation6 Participants
Direct Laryngoscope GroupEsophageal Intubation9 Participants
Other Pre-specified

ICU-free Days in the First 28 Days

Time frame: 28 days

ArmMeasureValue (MEDIAN)
Video Laryngoscope GroupICU-free Days in the First 28 Days20 days
Direct Laryngoscope GroupICU-free Days in the First 28 Days19 days
Other Pre-specified

Injury to the Teeth

Time frame: from induction to 2 minutes following tracheal intubation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupInjury to the Teeth3 Participants
Direct Laryngoscope GroupInjury to the Teeth2 Participants
Other Pre-specified

Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube

Time frame: Duration of procedure (minutes)

Population: Data was not available for entire patient population.

ArmMeasureGroupValue (NUMBER)
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeEndotracheal Tube - 3+15 number of events
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 1316 number of events
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeEndotracheal Tube - 243 number of events
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 219 number of events
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 0364 number of events
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 3+6 number of events
Video Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeEndotracheal Tube - 1646 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 3+27 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeEndotracheal Tube - 1620 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeEndotracheal Tube - 266 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeEndotracheal Tube - 3+19 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 0330 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 1317 number of events
Direct Laryngoscope GroupNumber of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal TubeBougie - 233 number of events
Other Pre-specified

Number of Laryngoscopy Attempts

Time frame: Duration of procedure (minutes)

Population: A subset of patients were missing this data variable.

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupNumber of Laryngoscopy AttemptsNumber of times a laryngoscope entered the patient's mouth (reported by observer) - 1636 Participants
Video Laryngoscope GroupNumber of Laryngoscopy AttemptsNumber of times a laryngoscope entered the patient's mouth (reported by observer) - 254 Participants
Video Laryngoscope GroupNumber of Laryngoscopy AttemptsNumber of times a laryngoscope entered the patient's mouth (reported by observer) - 3+14 Participants
Direct Laryngoscope GroupNumber of Laryngoscopy AttemptsNumber of times a laryngoscope entered the patient's mouth (reported by observer) - 1546 Participants
Direct Laryngoscope GroupNumber of Laryngoscopy AttemptsNumber of times a laryngoscope entered the patient's mouth (reported by observer) - 2127 Participants
Direct Laryngoscope GroupNumber of Laryngoscopy AttemptsNumber of times a laryngoscope entered the patient's mouth (reported by observer) - 3+33 Participants
Other Pre-specified

Operator-reported Aspiration

Time frame: from induction to 2 minutes following tracheal intubation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupOperator-reported Aspiration7 Participants
Direct Laryngoscope GroupOperator-reported Aspiration12 Participants
Other Pre-specified

Reason for Failure to Intubate on the First Attempt

Providers could give more than one reason for failure to intubate on the first attempt for each intubation (not mutually exclusive). In addition, data on the reason for failure to intubate on the first attempt was missing for 23 patients in the video laryngoscope group and 40 patients in the direct laryngoscope group. Reason for failure among those who did not meet the primary outcome (successful intubation on the first attempt): * Inadequate view of the larynx * Inability to intubate the trachea with an endotracheal tube * Inability to cannulate the trachea with a bougie * Attempt aborted due to change in patient condition (e.g., worsening hypoxemia, hypotension, bradycardia, vomiting, bleeding) * Technical failure of the laryngoscope (e.g., battery, light source, camera, screen) * Other * Not Reported

Time frame: Duration of procedure (minutes)

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptInability to cannulate the trachea with a bougie7 Participants
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptTechnical failure of the laryngoscope (e.g., battery, light source, camera, screen)2 Participants
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptInability to intubate the trachea with an endotracheal tube44 Participants
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptOther13 Participants
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptAttempt aborted due to change in patient condition2 Participants
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptNot Reported23 Participants
Video Laryngoscope GroupReason for Failure to Intubate on the First AttemptInadequate view of the larynx26 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptNot Reported40 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptInadequate view of the larynx123 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptInability to intubate the trachea with an endotracheal tube32 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptInability to cannulate the trachea with a bougie19 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptAttempt aborted due to change in patient condition14 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptTechnical failure of the laryngoscope (e.g., battery, light source, camera, screen)4 Participants
Direct Laryngoscope GroupReason for Failure to Intubate on the First AttemptOther10 Participants
Other Pre-specified

Successful Intubation on the First Attempt Without a Severe Complication

This outcome reports the number of participants that experienced successful intubation on the first attempt without experiencing complications, a composite of two independent outcomes: successful intubation on the first attempt (the primary outcome of the trial) and severe complication (the secondary outcome of the trial).

Time frame: from induction to 2 minutes following tracheal intubation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Video Laryngoscope GroupSuccessful Intubation on the First Attempt Without a Severe Complication484 Participants
Direct Laryngoscope GroupSuccessful Intubation on the First Attempt Without a Severe Complication420 Participants
Other Pre-specified

Ventilator Free Days in the First 28 Days

Time frame: 28 days

ArmMeasureValue (MEDIAN)
Video Laryngoscope GroupVentilator Free Days in the First 28 Days24 days
Direct Laryngoscope GroupVentilator Free Days in the First 28 Days23 days

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026