Multiple Trauma/Injuries Clinical Trial
— REACT-2Official title:
Randomized Study of Early Assessment by CT Scanning in Trauma Patients
Verified date | February 2018 |
Source | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 1083 |
Est. completion date | December 2014 |
Est. primary completion date | July 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Trauma patient with presence of one of the following criteria: At least one of the following parameters at hospital arrival: 1. Respiratory rate =30/min or =10/min 2. Pulse =120/min; 3. Systolic blood pressure =100 mmHg 4. Estimated external blood loss =500 ml 5. Glasgow Coma Score =13 6. Abnormal pupillary light reflex. Or clinical suspicion of one of the following diagnoses: 1. Fractures from at least two long bones 2. Multiple rib fractures, flail chest or open chest 3. Severe abdominal injury 4. Pelvic fracture 5. Unstable vertebral fractures or signs of spinal cord injury. Or one of the following injury mechanisms: 1. Fall from height (= 10 feet) 2. Ejection from the vehicle 3. Death occupant in same vehicle 4. Severely injured patient in same vehicle 5. Wedged or trapped chest / abdomen. Exclusion Criteria: 1. Age <18 years (if known) 2. Known pregnancy 3. Patients referred from other hospitals 4. Clearly low-energy trauma with blunt injury mechanism 5. Penetrating injury in 1 body region (except gun shot wounds) as the clearly isolated injury 6. 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. |
Country | Name | City | State |
---|---|---|---|
Netherlands | Academic Medical Center (AMC) | Amsterdam | |
Netherlands | University Medical Center Groningen | Groningen | |
Netherlands | University Medical Centre Nijmegen | Nijmegen | |
Netherlands | Erasmus Medical Center | Rotterdam | |
Switzerland | University Hospital Basel | Basel |
Lead Sponsor | Collaborator |
---|---|
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) | Erasmus Medical Center, University Hospital, Basel, Switzerland, University Medical Center Groningen, University Medical Center Nijmegen |
Netherlands, Switzerland,
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* Note: There are 35 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | In-hospital mortality. | Mortality during hospital admission. | From date of randomization until the date of death from any cause, while being an inpatient, assessed up to 1 year. | |
Secondary | Overall mortality | Mortality in general during specific time frames. | 24-hour, 30-day and 1-year mortality. | |
Secondary | Several clinical relevant time intervals. | time of arrival; time to CT; scanning time; time to diagnosis; time in the trauma room; time to intervention. |
From date and time of randomization to date and time of immediate intervention or ICU arrival, with an expected duration of 1-3 hours. | |
Secondary | Radiation exposure | Radiation dose in miliSievert. | Until six months posttrauma. | |
Secondary | Quality of life | As recorded by completing the EuroQol-6D. | Six and twelve months posttrauma. | |
Secondary | Morbidity | complications and total number of (re-)interventions and re-admissions; transfusion requirements; length of ICU stay; number of ventilation days. |
Up to six months posttrauma. | |
Secondary | General health | As recorded by completing the HUI-3. | Six and twelve months posttrauma. | |
Secondary | 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. |
Until six months posttrauma. |
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