A Multicenter, Randomized Study of Early Assessment by CT Scanning in Severely Injured Trauma Patients (REACT-2)
Primary Purpose
Multiple Trauma/Injuries
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Total body Computed Tomography.
Conventional imaging and selective CT scanning.
Sponsored by
About this trial
This is an interventional diagnostic trial for Multiple Trauma/Injuries focused on measuring Trauma, Injur*, Emergen*, Computed Tomography, Total body, TBCT, Whole body, WBCT, Full body, Pan CT
Eligibility Criteria
Inclusion Criteria:
Trauma patient with presence of one of the following criteria:
At least one of the following parameters at hospital arrival:
- Respiratory rate ≥30/min or ≤10/min
- Pulse ≥120/min;
- Systolic blood pressure ≤100 mmHg
- Estimated external blood loss ≥500 ml
- Glasgow Coma Score ≤13
- Abnormal pupillary light reflex.
Or clinical suspicion of one of the following diagnoses:
- Fractures from at least two long bones
- Multiple rib fractures, flail chest or open chest
- Severe abdominal injury
- Pelvic fracture
- Unstable vertebral fractures or signs of spinal cord injury.
Or one of the following injury mechanisms:
- Fall from height (≥ 10 feet)
- Ejection from the vehicle
- Death occupant in same vehicle
- Severely injured patient in same vehicle
- Wedged or trapped chest / abdomen.
Exclusion Criteria:
- Age <18 years (if known)
- Known pregnancy
- Patients referred from other hospitals
- Clearly low-energy trauma with blunt injury mechanism
- Penetrating injury in 1 body region (except gun shot wounds) as the clearly isolated injury
- Any patient who is judged to be too unstable to undergo a CT scan and requires (cardiopulmonary) resuscitation or immediate operation because death is imminent.
Sites / Locations
- Academic Medical Center (AMC)
- University Medical Center Groningen
- University Medical Centre Nijmegen
- Erasmus Medical Center
- University Hospital Basel
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Conventional imaging
Immediate total body CT
Arm Description
The control group will be evaluated with X-rays, ultrasonography and selective CT scanning.
The intervention group will receive a 'total body' CT scan from head to pelvis. Conventional radiography and FAST will be completely omitted.
Outcomes
Primary Outcome Measures
In-hospital mortality.
Mortality during hospital admission.
Secondary Outcome Measures
Overall mortality
Mortality in general during specific time frames.
Several clinical relevant time intervals.
time of arrival;
time to CT;
scanning time;
time to diagnosis;
time in the trauma room;
time to intervention.
Radiation exposure
Radiation dose in miliSievert.
Quality of life
As recorded by completing the EuroQol-6D.
Morbidity
complications and total number of (re-)interventions and re-admissions;
transfusion requirements;
length of ICU stay;
number of ventilation days.
General health
As recorded by completing the HUI-3.
Cost-effectiveness analyses.
Cost-effectiveness analyses will be performed with the costs per patient alive and costs per patient alive without serious morbidity as outcome measures.
Additionally, a cost-utility analysis will be done with the cost per QALY as outcome measure. Incremental cost-effectiveness ratios will be calculated, expressing the extra costs per (i) extra patients alive, (ii) extra patients alive and without serious morbidity, and (iii) additional QALY.
Full Information
NCT ID
NCT01523626
First Posted
January 20, 2012
Last Updated
February 4, 2018
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
University Medical Center Nijmegen, Erasmus Medical Center, University Medical Center Groningen, University Hospital, Basel, Switzerland
1. Study Identification
Unique Protocol Identification Number
NCT01523626
Brief Title
A Multicenter, Randomized Study of Early Assessment by CT Scanning in Severely Injured Trauma Patients
Acronym
REACT-2
Official Title
Randomized Study of Early Assessment by CT Scanning in Trauma Patients
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
University Medical Center Nijmegen, Erasmus Medical Center, University Medical Center Groningen, University Hospital, Basel, Switzerland
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Computed tomography (CT) scanning has become essential in the early diagnostic phase of trauma care because of its high diagnostic accuracy. The introduction of multi-slice CT scanners and infrastructural improvements made 'total body' CT scanning (TBCT) technically feasible and its usage is currently becoming common practice in several trauma centers.
However, literature provides limited evidence whether immediate 'total body' CT scanning leads to better clinical outcome then conventional radiographic imaging supplemented with selective CT scanning in trauma patients. The aim of the REACT-2 trial is to determine the value of immediate TBCT scanning in trauma patients.
The investigators hypothesize that immediate 'total body' CT scanning during the primary survey of severely injured trauma patients has positive effects on patient outcome compared with standard conventional ATLS based radiological imaging supplemented with selective CT scanning.
Detailed Description
Injuries are the cause of 5.8 million deaths annually which accounts for almost 10% of global mortality. Among adults aged 15-59 years the proportion of injuries as cause of death is even higher, ranging from 22% to 29% [1].
Specialized trauma centers all over the world provide initial trauma care and diagnostic work-up of trauma patients. This work-up is standardized and frequently based on the Advanced Trauma Life Support (ATLS) guidelines which include a fast and priority-based physical examination as well as screening radiographs supplemented with selective Computed Tomography scanning (CT). ATLS guidelines advise to routinely perform X-rays of thorax and pelvis and Focused Assessment with Sonography for Trauma (FAST) in trauma patients. Whether or not to perform CT scanning following conventional imaging is defined less clearly in the ATLS guidelines and depends upon national guidelines and local protocols.
In recent years CT scanning has become faster, more detailed and more available in the acute trauma care setting. CT shows high accuracy for a wide range of injuries which is reflected by a low missed diagnosis rate. Hence, the conventional radiological work-up according to the ATLS may not be the optimal choice of primary diagnostics anymore. Furthermore, severely injured patients frequently require secondary CT scanning of many parts of the body after conventional imaging. Modern multidetector CT scanners (MDCT) can perform imaging of the head, cervical spine, chest, abdomen and pelvis in a single examination ('total body' CT scanning). The past few years this 'total body' imaging concept gained popularity as a possible alternative to the conventional imaging strategy. With the use of immediate 'total body' CT (TBCT) scanning in trauma patients, rapid and detailed information of organ and tissue injury becomes available and a well-founded plan for further therapy can be made.
In the past, CT scanners were located in the radiology department, frequently even on another floor than the emergency department (ED) were the trauma patient is admitted. The past assumption that TBCT in severely injured trauma patients is too time consuming may no longer be held, since an increasing number of trauma centers have a CT scanner available at the ED or even in the trauma room itself. Several studies evaluated time intervals associated with TBCT usage in severely injured patients. Although these studies are incomparable with respect to design, CT scanners used, diagnostic work-up protocols and trauma populations, the main conclusion is clear. TBCT scanning in trauma patients is not as time consuming as was once expected and may even be time saving compared to conventional imaging protocols supplemented with selective CT.
More and more trauma centers encourage and are implementing immediate TBCT scanning in the diagnostic phase of primary trauma care. Since the burden of TBCT in terms of costs and radiation dose is at least controversial, the advantage of performing immediate TBCT should be proven in high quality studies resulting in high level evidence in order to make its implementation justifiable.
In order to assess the value of immediate TBCT scanning in severely injured trauma patients, the Academic Medical Center (AMC) in Amsterdam, the Netherlands, has initiated an international multicenter randomized clinical trial. Severely injured patients, who are thought to benefit the most from a 'total body' imaging concept, will be included.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Trauma/Injuries
Keywords
Trauma, Injur*, Emergen*, Computed Tomography, Total body, TBCT, Whole body, WBCT, Full body, Pan CT
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1083 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Conventional imaging
Arm Type
Other
Arm Description
The control group will be evaluated with X-rays, ultrasonography and selective CT scanning.
Arm Title
Immediate total body CT
Arm Type
Other
Arm Description
The intervention group will receive a 'total body' CT scan from head to pelvis. Conventional radiography and FAST will be completely omitted.
Intervention Type
Other
Intervention Name(s)
Total body Computed Tomography.
Other Intervention Name(s)
Whole body CT, Pan CT, Full body CT, TBCT, WBCT
Intervention Description
The CT protocol for the intervention group consists of a two-step whole-body acquisition (from vertex to pubic symphysis) starting with Head and Neck Non Enhanced CT (NECT) with arms alongside the body.
The preferred technique for the second complementary scan is a split-bolus intravenous contrast directly after repositioning of the arms alongside the head, and this second scan covers thorax, abdomen and pelvis. Participating centers however are free to choose their own technique as long as intravenous contrast is given for the chest and abdominal part of the TBCT.
Intervention Type
Other
Intervention Name(s)
Conventional imaging and selective CT scanning.
Other Intervention Name(s)
X-rays, FAST, Conventional radiography, Computed Tomography, CT
Intervention Description
The control group will be evaluated according to a conventional trauma protocol with X-rays (of the chest and pelvis), ultrasonography (Focused Assessment with Sonography for Trauma (FAST)) and selective CT scanning.
Indications for the selective CT scanning are pre-defined and based on the combined local protocols of the participating centers.
Primary Outcome Measure Information:
Title
In-hospital mortality.
Description
Mortality during hospital admission.
Time Frame
From date of randomization until the date of death from any cause, while being an inpatient, assessed up to 1 year.
Secondary Outcome Measure Information:
Title
Overall mortality
Description
Mortality in general during specific time frames.
Time Frame
24-hour, 30-day and 1-year mortality.
Title
Several clinical relevant time intervals.
Description
time of arrival;
time to CT;
scanning time;
time to diagnosis;
time in the trauma room;
time to intervention.
Time Frame
From date and time of randomization to date and time of immediate intervention or ICU arrival, with an expected duration of 1-3 hours.
Title
Radiation exposure
Description
Radiation dose in miliSievert.
Time Frame
Until six months posttrauma.
Title
Quality of life
Description
As recorded by completing the EuroQol-6D.
Time Frame
Six and twelve months posttrauma.
Title
Morbidity
Description
complications and total number of (re-)interventions and re-admissions;
transfusion requirements;
length of ICU stay;
number of ventilation days.
Time Frame
Up to six months posttrauma.
Title
General health
Description
As recorded by completing the HUI-3.
Time Frame
Six and twelve months posttrauma.
Title
Cost-effectiveness analyses.
Description
Cost-effectiveness analyses will be performed with the costs per patient alive and costs per patient alive without serious morbidity as outcome measures.
Additionally, a cost-utility analysis will be done with the cost per QALY as outcome measure. Incremental cost-effectiveness ratios will be calculated, expressing the extra costs per (i) extra patients alive, (ii) extra patients alive and without serious morbidity, and (iii) additional QALY.
Time Frame
Until six months posttrauma.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Trauma patient with presence of one of the following criteria:
At least one of the following parameters at hospital arrival:
Respiratory rate ≥30/min or ≤10/min
Pulse ≥120/min;
Systolic blood pressure ≤100 mmHg
Estimated external blood loss ≥500 ml
Glasgow Coma Score ≤13
Abnormal pupillary light reflex.
Or clinical suspicion of one of the following diagnoses:
Fractures from at least two long bones
Multiple rib fractures, flail chest or open chest
Severe abdominal injury
Pelvic fracture
Unstable vertebral fractures or signs of spinal cord injury.
Or one of the following injury mechanisms:
Fall from height (≥ 10 feet)
Ejection from the vehicle
Death occupant in same vehicle
Severely injured patient in same vehicle
Wedged or trapped chest / abdomen.
Exclusion Criteria:
Age <18 years (if known)
Known pregnancy
Patients referred from other hospitals
Clearly low-energy trauma with blunt injury mechanism
Penetrating injury in 1 body region (except gun shot wounds) as the clearly isolated injury
Any patient who is judged to be too unstable to undergo a CT scan and requires (cardiopulmonary) resuscitation or immediate operation because death is imminent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
J Carel Goslings, PhD
Organizational Affiliation
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Academic Medical Center (AMC)
City
Amsterdam
ZIP/Postal Code
1105AZ
Country
Netherlands
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands
Facility Name
University Medical Centre Nijmegen
City
Nijmegen
ZIP/Postal Code
6525 GA
Country
Netherlands
Facility Name
Erasmus Medical Center
City
Rotterdam
ZIP/Postal Code
3015 CE
Country
Netherlands
Facility Name
University Hospital Basel
City
Basel
ZIP/Postal Code
CH - 4031
Country
Switzerland
12. IPD Sharing Statement
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A Multicenter, Randomized Study of Early Assessment by CT Scanning in Severely Injured Trauma Patients
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