Early Versus Late Intubation Trial in Physician Manned Emergency Medical Services (ELITE)
Primary Purpose
Trauma, Craniocerebral Trauma, Intracerebral Hemorrhage
Status
Withdrawn
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Early Intubation
Late intubation
Sponsored by
About this trial
This is an interventional treatment trial for Trauma
Eligibility Criteria
Inclusion Criteria:
- Adult patients (> 18 years)
- Initial GCS < 9 independent of cause.
- Intact airway reflexes and no impending airway obstruction.
- Located < 20 min ambulance transport time from nearest hospital emergency department.
Exclusion Criteria:
- Pediatric patients (under 18 years).
- Primary cardiorespiratory arrest (of non-traumatic / medical cause).
- Planned helicopter transport to hospital.
Sites / Locations
- Haukeland University Hospital
- Norwegian Air Ambulance Foundation
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Early Intubation
Late intubation
Arm Description
Early intubation is defined as prehospital intubation on the scene of the patient illness/injury, or where the EMS physician first meets the patient (e.g en route to hospital). Intubation includes drug assisted and/or rapid sequence intubation (RSI) with endotracheal tube.
Late intubation is defined as on-scene prehospital high-flow (> 10 L/min) supplemental oxygen by mask, assisted bag-mask-ventilation by EMS physician if required and stable recovery position during transport to hospital. Intubation should be done on arrival in the emergency department.
Outcomes
Primary Outcome Measures
30 days mortality after injury or illness.
Dead or alive
Neurologic outcome at 6 months after injury or illness.
Neurologic outcome will be assessed using glascow outcome scores (GOS-E)
Secondary Outcome Measures
Intubation success rates and airway management complications for the entire cohort and for key subsets
Length of hospital stay, complications and degree of disability at discharge.
Prevalence of adverse effects like cardiovascular complications (e.g. bradycardia, hypotension, asystole), and respiratory complications (e.g. hypoxia, pneumothorax).
Full Information
NCT ID
NCT01730001
First Posted
November 10, 2012
Last Updated
September 18, 2017
Sponsor
Norwegian Air Ambulance Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01730001
Brief Title
Early Versus Late Intubation Trial in Physician Manned Emergency Medical Services
Acronym
ELITE
Official Title
A Prospective Randomized Controlled Trial Comparing Competent EARLY-intubation to LATE-intubation in Patients With Prehospital GCS < 9 and Short Transport Time to Hospital.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Withdrawn, no patients included
Study Start Date
January 1, 2015 (Anticipated)
Primary Completion Date
March 28, 2017 (Actual)
Study Completion Date
March 28, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian Air Ambulance Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study looks at advanced airway management in critically ill or injured patients treated by physician manned emergency medical services, comparing early (on-scene) intubation to late (emergency department) intubation.
Detailed Description
The ELITE trial is a prospective randomized controlled trial (RCT) to compare competent EARLY-intubation to LATE-intubation in patients with on-scene Glasgow Coma Scale (GCS) < 9 and short ambulance transport times (< 20 min) to hospital.
The study aims to establish if advanced airway management with endotracheal intubation (ETI) in the field by specially trained Emergency Medical Services (EMS) physicians - compared to endotracheal intubation (ETI) performed by physicians in the emergency department in the same group - improves outcome in terms of 30-day mortality, degree of disability at discharge, complications and length of hospital stay, and neurologic outcome at 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trauma, Craniocerebral Trauma, Intracerebral Hemorrhage, Seizures, Unconsciousness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Early Intubation
Arm Type
Active Comparator
Arm Description
Early intubation is defined as prehospital intubation on the scene of the patient illness/injury, or where the EMS physician first meets the patient (e.g en route to hospital). Intubation includes drug assisted and/or rapid sequence intubation (RSI) with endotracheal tube.
Arm Title
Late intubation
Arm Type
Active Comparator
Arm Description
Late intubation is defined as on-scene prehospital high-flow (> 10 L/min) supplemental oxygen by mask, assisted bag-mask-ventilation by EMS physician if required and stable recovery position during transport to hospital. Intubation should be done on arrival in the emergency department.
Intervention Type
Procedure
Intervention Name(s)
Early Intubation
Intervention Type
Procedure
Intervention Name(s)
Late intubation
Primary Outcome Measure Information:
Title
30 days mortality after injury or illness.
Description
Dead or alive
Time Frame
30 days after illness or injury
Title
Neurologic outcome at 6 months after injury or illness.
Description
Neurologic outcome will be assessed using glascow outcome scores (GOS-E)
Time Frame
6 months after illness or injury
Secondary Outcome Measure Information:
Title
Intubation success rates and airway management complications for the entire cohort and for key subsets
Time Frame
up to 6 months after illness or injury
Title
Length of hospital stay, complications and degree of disability at discharge.
Time Frame
up to 6 months after illness or injury
Title
Prevalence of adverse effects like cardiovascular complications (e.g. bradycardia, hypotension, asystole), and respiratory complications (e.g. hypoxia, pneumothorax).
Time Frame
up to 6 months after illness or injury
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients (> 18 years)
Initial GCS < 9 independent of cause.
Intact airway reflexes and no impending airway obstruction.
Located < 20 min ambulance transport time from nearest hospital emergency department.
Exclusion Criteria:
Pediatric patients (under 18 years).
Primary cardiorespiratory arrest (of non-traumatic / medical cause).
Planned helicopter transport to hospital.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Geir A Sunde, MD
Organizational Affiliation
Norwegian Air Ambulance Foundation
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stephen JM Sollid, MD, PhD, Ass.Prof
Organizational Affiliation
Norwegian Air Ambulance Foundation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Hans M Lossius, MD, PhD, Prof
Organizational Affiliation
Norwegian Air Ambulance Foundation
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Espen Fevang, MD
Organizational Affiliation
Norwegian Air Ambulance Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haukeland University Hospital
City
Bergen
ZIP/Postal Code
5021
Country
Norway
Facility Name
Norwegian Air Ambulance Foundation
City
Drøbak
ZIP/Postal Code
1441
Country
Norway
12. IPD Sharing Statement
Links:
URL
http://www.norskluftambulanse.no
Description
Norwegian Air Ambulance Foundation
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Early Versus Late Intubation Trial in Physician Manned Emergency Medical Services
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