Drug Order for Rapid Sequence Intubation (DO-RSI)
Primary Purpose
Acute Respiratory Failure
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Rapid sequence intubation: sedative first
Rapid sequence intubation: paralytic first
Sponsored by
About this trial
This is an interventional other trial for Acute Respiratory Failure
Eligibility Criteria
Inclusion Criteria:
- The patient must be undergoing orotracheal intubation in the Emergency Department
- The patient must be receiving both a sedative and paralytic immediately prior to intubation (i.e. undergoing rapid sequence intubation).
- The patient must be presumed to be 18 years of age or older at the time of enrollment.
Exclusion Criteria:
- Prisoner or in custody
- Known or suspected to be pregnant, based on the opinion of the attending physician.
- Intubation performed by a physician assistant (this is rarely done in our ED; each physician assistant intubates less than twice per year, so the intubation outcomes would hinge more on their experience rather than drug order).
Sites / Locations
- Hennepin County Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Sedative first
Paralytic agent first
Arm Description
Rapid sequence intubation: sedative first
Rapid sequence intubation: paralytic first
Outcomes
Primary Outcome Measures
Time elapsed from drug administration to intubation attempt end
The primary outcome will be time from complete administration of the first medication to successful first attempt intubation. This timing period will begin when the first RSI agent is completely administered and end when the laryngoscope blade is removed from the mouth. Attempts that are not successful on the first attempt will be excluded from the primary outcome measure because the time to intubation will be confounded by the failure; in these cases the altered duration will have more to do with device or patient characteristics than with drug order.
Secondary Outcome Measures
Duration of first intubation attempt
Defined as the time elapsed between inserting and removing the laryngoscope blade from the mouth. The primary outcome, duration of the first intubation attempt, and apnea duration will only be measured in those with a successful first attempt.
Hypoxemia
Oxygen saturation < 90%, during the time interval between the start of the intubation attempt and 1 minute following completion of the attempt.
Best laryngeal view
Cormack-Lehane grade
Best laryngeal view
Percent of glottic opening
First intubation attempt success
Defined as successful intubation with a single insertion of the laryngoscope, regardless of the number of passages of the endotracheal tube or bougie.
Full Information
NCT ID
NCT03420950
First Posted
January 28, 2018
Last Updated
January 19, 2022
Sponsor
Hennepin Healthcare Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT03420950
Brief Title
Drug Order for Rapid Sequence Intubation
Acronym
DO-RSI
Official Title
Drug Order for Rapid Sequence Intubation in Emergency Department Intubation
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
February 5, 2018 (Actual)
Primary Completion Date
September 29, 2021 (Actual)
Study Completion Date
September 29, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hennepin Healthcare Research Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a randomized, blinded trial comparing the order of drug administration for rapid sequence intubation in the Emergency Department.
Detailed Description
Based on data (excluding outliers) from protocol 16-4146, the intubation time with the paralytic and sedative first administered is 86 s, and 93 s, respectively, with a standard deviation of approximately 25-30 s. Using these assumptions, 470 patients (235 per group) will need to be enrolled to detect an 7 s absolute difference between groups with 80% power.
Because a greater difference is anticipated in those who receive rocuronium rather than succinylcholine (because succinylcholine takes action faster), goal enrollment is 470 patients who receive rocuronium as the paralytic who are intubated successfully on the first attempt. The total enrollment will be higher, accounting for those who receive succinylcholine and those who are not successful on the first attempt. The data for those who receive succinylcholine first will be reported and is planned to be used to determine the feasibility of a future trial.
The primary group of analysis will be those receiving rocuronium, because this medication acts somewhat slower than succinylcholine. Patients who receive either drug will be analyzed, but it is pre-specified that the group of interest are those receiving rocuronium.
The primary outcome, first intubation attempt duration, and apnea duration will be measured only in those with a successful first attempt because these timing events will be confounded by attempt failure; in these cases the altered duration will have more to do with device or patient characteristics than with drug order.
The remainder of the outcomes will be measured in all enrolled subjects in an intention to treat analysis.
An analysis for patients by RSI drug order actually received, regardless of treatment allocation, will also be presented.
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
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The nurse administering the drug is not blinded, but the outcome assessor and physician performing the intubation are blinded to drug order.
Allocation
Randomized
Enrollment
335 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sedative first
Arm Type
Other
Arm Description
Rapid sequence intubation: sedative first
Arm Title
Paralytic agent first
Arm Type
Other
Arm Description
Rapid sequence intubation: paralytic first
Intervention Type
Other
Intervention Name(s)
Rapid sequence intubation: sedative first
Intervention Description
Sedative first
Intervention Type
Other
Intervention Name(s)
Rapid sequence intubation: paralytic first
Intervention Description
Paralytic first
Primary Outcome Measure Information:
Title
Time elapsed from drug administration to intubation attempt end
Description
The primary outcome will be time from complete administration of the first medication to successful first attempt intubation. This timing period will begin when the first RSI agent is completely administered and end when the laryngoscope blade is removed from the mouth. Attempts that are not successful on the first attempt will be excluded from the primary outcome measure because the time to intubation will be confounded by the failure; in these cases the altered duration will have more to do with device or patient characteristics than with drug order.
Time Frame
5 minutes
Secondary Outcome Measure Information:
Title
Duration of first intubation attempt
Description
Defined as the time elapsed between inserting and removing the laryngoscope blade from the mouth. The primary outcome, duration of the first intubation attempt, and apnea duration will only be measured in those with a successful first attempt.
Time Frame
5 minutes
Title
Hypoxemia
Description
Oxygen saturation < 90%, during the time interval between the start of the intubation attempt and 1 minute following completion of the attempt.
Time Frame
5 minutes
Title
Best laryngeal view
Description
Cormack-Lehane grade
Time Frame
5 minutes
Title
Best laryngeal view
Description
Percent of glottic opening
Time Frame
5 minutes
Title
First intubation attempt success
Description
Defined as successful intubation with a single insertion of the laryngoscope, regardless of the number of passages of the endotracheal tube or bougie.
Time Frame
5 minutes
Other Pre-specified Outcome Measures:
Title
Memory of intubation
Description
A structured questionnaire will be administered to patients after extubation. We will attempt to approach all enrolled patients, but realize that some will be unreachable due to death, head injury, rapid discharge from the hospital, and other reason.
Time Frame
1 week (approximately)
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 Emergency Department
The patient must be receiving both a sedative and paralytic immediately prior to intubation (i.e. undergoing rapid sequence intubation).
The patient must be presumed to be 18 years of age or older at the time of enrollment.
Exclusion Criteria:
Prisoner or in custody
Known or suspected to be pregnant, based on the opinion of the attending physician.
Intubation performed by a physician assistant (this is rarely done in our ED; each physician assistant intubates less than twice per year, so the intubation outcomes would hinge more on their experience rather than drug order).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian Driver, MD
Organizational Affiliation
Hennepin County Medical Center, Minneapolis
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hennepin County Medical Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55415
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Drug Order for Rapid Sequence Intubation
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