Complications are common during tracheal intubations performed outside of the operating room. Successful intubation on the first attempt has been associated with a lower rate of procedural complications, but the proportion of critically ill patients intubated on the first attempt during tracheal intubations outside of the operating room is less than 90%. The bougie, a thin semi-rigid tube that can be placed into the trachea, allowing a Seldinger-like technique of intubating a patient's airway, has been traditionally reserved for difficult or failed airways. However, a recent single center trial of adult patients intubated in an emergency department demonstrated that use of the bougie on the first attempt improved intubation success, compared to use of a traditional stylet.
Theinvestigators propose a multi-center randomized trial to compare first-attempt bougie use versus endotracheal tube with stylet use for tracheal intubation of critically ill adults in the ED and ICU.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Acute Respiratory Failure | Other: Bougie Other: Endotracheal Tube with Stylet | Not Applicable |
The BOUGIE trial is a prospective, parallel group, pragmatic, randomized trial comparing the effect of bougie use versus endotracheal tube with stylet use on the incidence of successful intubation on the first attempt among adults undergoing urgent or emergent tracheal intubation.
Patients admitted to the study units who are deemed by their clinical team to require intubation and fulfill inclusion criteria without meeting exclusion criteria will be randomized 1:1 to use of a bougie or use of an endotracheal tube and stylet on the first attempt at intubation. All other decisions regarding airway management, including the choice to use a bougie or endotracheal tube and stylet on subsequent attempts, will remain at the discretion of the treating provider.
The trial will enroll 1,106 patients. Conduct of the trial will be overseen by a Data Safety Monitoring Board. An interim analysis will be performed after the enrollment of 553 patients. The analysis of the trial will be conducted in accordance with a pre-specified statistical analysis plan, which will be submitted for publication or made publicly available prior to the conclusion of enrollment.
The primary outcome is successful intubation on the first attempt
The secondary outcome is severe hypoxemia (lowest arterial oxygen saturation between induction and two minutes following intubation of less than 80%)
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 1106 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Bougie or Stylet In Patients Undergoing Intubation Emergently (BOUGIE): a Randomized, Multi-center Trial |
| Actual Study Start Date : | April 29, 2019 |
| Actual Primary Completion Date : | February 14, 2021 |
| Actual Study Completion Date : | March 13, 2021 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: BOUGIE
For patients randomized to use of a bougie, the operator will use a bougie on the first attempt at intubation. If successful, an assistant will load an endotracheal tube over the bougie, and the operator (without removing the laryngoscope from the mouth) will guide the tube through the vocal cords to the desired depth in the trachea. If the bougie is not successfully placed in the trachea or the endotracheal tube cannot be successfully advanced over the bougie on the first attempt at intubation, the operator may use any approach during subsequent attempts at tracheal intubation. |
Other: Bougie
disposable tracheal tube introducer of approximately 70 cm in length
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Active Comparator: Endotracheal Tube with Stylet
For patients randomized to use of an endotracheal tube with stylet, the operator will use an endotracheal tube containing a removeable, malleable stylet, on the first attempt at intubation. Manipulation of the shape/curve of the endotracheal tube with stylet is at the discretion of the operator, however a "straight-to-cuff" shape and a bend angle of 25° to 35° is encouraged. The stylet will be left in place until the tube is advanced to the trachea. If the endotracheal tube with stylet is not successfully placed in the trachea on the first attempt at intubation, the operator may use any approach during subsequent attempts at tracheal intubation. |
Other: Endotracheal Tube with Stylet
endotracheal tube preloaded with a removable, malleable stylet
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Defined as any of:
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
| United States, Alabama | |
| University of Alabama at Birmingham | |
| Birmingham, Alabama, United States, 35233 | |
| United States, Colorado | |
| University of Colorado | |
| Denver, Colorado, United States, 80045 | |
| Denver Health and Hospital Authority | |
| Denver, Colorado, United States, 80204 | |
| United States, Iowa | |
| University of Iowa Hospital | |
| Iowa City, Iowa, United States, 52242 | |
| United States, Louisiana | |
| Louisiana State University School of Medicine | |
| New Orleans, Louisiana, United States, 70112 | |
| Ochsner Medical Center | Ochsner Health System | |
| New Orleans, Louisiana, United States, 70112 | |
| United States, New York | |
| Lincoln Medical Center | |
| Bronx, New York, United States, 10451 | |
| United States, North Carolina | |
| Duke University Medical Center | |
| Durham, North Carolina, United States, 27710 | |
| Wake Forest Baptist Health | |
| Lexington, North Carolina, United States, 27292 | |
| United States, Tennessee | |
| Vanderbilt University Medical Center | |
| Nashville, Tennessee, United States, 37209 | |
| United States, Washington | |
| Harborview Medical Center, University of Washington | |
| Seattle, Washington, United States, 98104 | |
| Study Director: | Jonathan D Casey, MD | Vanderbilt University Medical Center | |
| Study Chair: | Matthew W Semler, MD, MSc | Vanderbilt University Medical Center | |
| Principal Investigator: | Brian E Driver, MD | Hennepin County Medical Center, Minneapolis | |
| Principal Investigator: | Matthew E Prekker, MD | Hennepin County Medical Center, Minneapolis |
| Tracking Information | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| First Submitted Date ICMJE | April 19, 2019 | ||||||||||||
| First Posted Date ICMJE | April 26, 2019 | ||||||||||||
| Last Update Posted Date | March 22, 2021 | ||||||||||||
| Actual Study Start Date ICMJE | April 29, 2019 | ||||||||||||
| Actual Primary Completion Date | February 14, 2021 (Final data collection date for primary outcome measure) | ||||||||||||
| Current Primary Outcome Measures ICMJE |
Number of intubations with successful intubation on the first attempt [ Time Frame: from induction to 2 minutes following tracheal intubation ] The primary outcome is successful intubation on the first attempt. Successful intubation on the first attempt is defined as placement of an endotracheal tube in the trachea (confirmed by standard means including capnography) following: (1) a single insertion of a laryngoscope blade into the mouth and (2) EITHER a single insertion of a bougie into the mouth followed by a single insertion of an endotracheal tube into the mouth OR a single insertion of an endotracheal tube with stylet into the mouth.
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| Original Primary Outcome Measures ICMJE | Same as current | ||||||||||||
| Change History | |||||||||||||
| Current Secondary Outcome Measures ICMJE |
Number of intubations with severe hypoxemia [ Time Frame: from induction to 2 minutes following tracheal intubation ] Defined as an oxygen saturation less than 80% during the time interval from induction to two minutes after completion of the intubation procedure
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| Original Secondary Outcome Measures ICMJE | Same as current | ||||||||||||
| Current Other Pre-specified Outcome Measures |
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| Original Other Pre-specified Outcome Measures |
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| Descriptive Information | |||||||||||||
| Brief Title ICMJE | Bougie or Stylet In Patients Undergoing Intubation Emergently (BOUGIE) | ||||||||||||
| Official Title ICMJE | Bougie or Stylet In Patients Undergoing Intubation Emergently (BOUGIE): a Randomized, Multi-center Trial | ||||||||||||
| Brief Summary |
Complications are common during tracheal intubations performed outside of the operating room. Successful intubation on the first attempt has been associated with a lower rate of procedural complications, but the proportion of critically ill patients intubated on the first attempt during tracheal intubations outside of the operating room is less than 90%. The bougie, a thin semi-rigid tube that can be placed into the trachea, allowing a Seldinger-like technique of intubating a patient's airway, has been traditionally reserved for difficult or failed airways. However, a recent single center trial of adult patients intubated in an emergency department demonstrated that use of the bougie on the first attempt improved intubation success, compared to use of a traditional stylet. Theinvestigators propose a multi-center randomized trial to compare first-attempt bougie use versus endotracheal tube with stylet use for tracheal intubation of critically ill adults in the ED and ICU. |
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| Detailed Description |
The BOUGIE trial is a prospective, parallel group, pragmatic, randomized trial comparing the effect of bougie use versus endotracheal tube with stylet use on the incidence of successful intubation on the first attempt among adults undergoing urgent or emergent tracheal intubation. Patients admitted to the study units who are deemed by their clinical team to require intubation and fulfill inclusion criteria without meeting exclusion criteria will be randomized 1:1 to use of a bougie or use of an endotracheal tube and stylet on the first attempt at intubation. All other decisions regarding airway management, including the choice to use a bougie or endotracheal tube and stylet on subsequent attempts, will remain at the discretion of the treating provider. The trial will enroll 1,106 patients. Conduct of the trial will be overseen by a Data Safety Monitoring Board. An interim analysis will be performed after the enrollment of 553 patients. The analysis of the trial will be conducted in accordance with a pre-specified statistical analysis plan, which will be submitted for publication or made publicly available prior to the conclusion of enrollment. The primary outcome is successful intubation on the first attempt The secondary outcome is severe hypoxemia (lowest arterial oxygen saturation between induction and two minutes following intubation of less than 80%) |
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| Study Type ICMJE | Interventional | ||||||||||||
| Study Phase ICMJE | Not Applicable | ||||||||||||
| Study Design ICMJE | Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment |
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| Condition ICMJE | Acute Respiratory Failure | ||||||||||||
| Intervention ICMJE |
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| Study Arms ICMJE |
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| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||||||
| Recruitment Status ICMJE | Completed | ||||||||||||
| Actual Enrollment ICMJE |
1106 | ||||||||||||
| Original Estimated Enrollment ICMJE | Same as current | ||||||||||||
| Actual Study Completion Date ICMJE | March 13, 2021 | ||||||||||||
| Actual Primary Completion Date | February 14, 2021 (Final data collection date for primary outcome measure) | ||||||||||||
| Eligibility Criteria ICMJE |
Inclusion Criteria:
Exclusion Criteria:
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| Sex/Gender ICMJE |
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| Ages ICMJE | 18 Years and older (Adult, Older Adult) | ||||||||||||
| Accepts Healthy Volunteers ICMJE | No | ||||||||||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||||||||||
| Listed Location Countries ICMJE | United States | ||||||||||||
| Removed Location Countries | |||||||||||||
| Administrative Information | |||||||||||||
| NCT Number ICMJE | NCT03928925 | ||||||||||||
| Other Study ID Numbers ICMJE | 182123 | ||||||||||||
| Has Data Monitoring Committee | Yes | ||||||||||||
| U.S. FDA-regulated Product |
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| IPD Sharing Statement ICMJE |
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| Responsible Party | Jonathan Casey, Vanderbilt University Medical Center | ||||||||||||
| Study Sponsor ICMJE | Vanderbilt University Medical Center | ||||||||||||
| Collaborators ICMJE | Not Provided | ||||||||||||
| Investigators ICMJE |
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| PRS Account | Vanderbilt University Medical Center | ||||||||||||
| Verification Date | March 2021 | ||||||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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