Prevention of HYPOthermia in TRAUMa Patients (HYPOTRAUM 2)
Primary Purpose
Trauma Patients
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
1: control group
2: interventional group
Sponsored by
About this trial
This is an interventional prevention trial for Trauma Patients focused on measuring Trauma, Prehospital, Hypothermia
Eligibility Criteria
Inclusion criteria :
- Patient with trauma (> 18 years)
- Pre-hospital management by MICU
- Scheduled transfer to a receiving center by a MICU
And at least one of the following criteria :
- Ambient temperature on the field < 18°C
- Body temperature <35°C on MICU arrival
- A Glasgow score < 15 on MICU arrival
- Systolic blood pressure < 100 mm Hg on MICU arrival
Exclusion criteria :
- Body temperature <31°C or >38°C
- Cardiac arrest before MICU arrival
- Bilateral ear bleeding preventing continuous monitoring of tympanic temperature
Sites / Locations
- SAMU 93, AP-HP, Urgences - SAMU 93, Unité Recherche-Enseignement-Qualité, Hôpital Avicenne
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
1: control group
2: interventional group
Arm Description
Classic - current management of trauma patients by French medical teams
Intervention Name : monitoring, treatment, control and prevention of hypothermia Continuous monitoring of body temperature Ambulance warming (target : 30°C) Patient warming with dedicated blanket Infusion fluid warming (and temperature control)
Outcomes
Primary Outcome Measures
Number of trauma patients arriving alive with a temperature > 35°C (at receiving hospital)
Secondary Outcome Measures
Survival at hospital discharge
Length of stay at hospital (days)
Full Information
NCT ID
NCT02575989
First Posted
September 15, 2015
Last Updated
August 17, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT02575989
Brief Title
Prevention of HYPOthermia in TRAUMa Patients
Acronym
HYPOTRAUM 2
Official Title
Prevention of HYPOthermia Before Admission in TRAUMa Patients - Hypotraum 2 Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
January 17, 2016 (Actual)
Primary Completion Date
October 16, 2019 (Actual)
Study Completion Date
January 16, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to demonstrate that the specific management will increase the number of alive trauma patient arriving with a temperature > 35°C.
Detailed Description
Trauma patients are often hypothermic (temperature < 35 °C) upon arrival at the hospital. Hypothermia is with hypotension and hypoxia, perfectly known to be directly responsible for complications.
Hypothermia is responsible, with acidosis and coagulopathy, of the " lethal triad" of trauma.
Thus, it is clearly established that hypothermia is directly associated with poor prognostic in trauma patients. In a recent study, mortality rate reached 100% for trauma patients arriving at the hospital with a body temperature below 32°C.
The weather, the severity of the trauma and medical (or paramedical) interventions are responsible for the onset of this hypothermia.
Then, continuous monitoring of the patient's temperature, active protection against hypothermia with a metal blanket, the warming (and measure the temperature of) infusion fluids, the warming (and measure the temperature of) the ambulance should improve patient's outcome. As hypothermia is associated with mortality of trauma patients, the control must lead to reduce mortality.
Randomization Due to the use of a global management strategy with combination of several specific interventions and the need for special equipment (heating devices infusion fluids), randomization will be done by investigator center: interventional center (combining the different interventions) and standard management (without modification, except measurements of the patient's and air temperature at inclusion and on arrival at a receiving center.
In this context, it is also crucial that the weather conditions, the characteristics of trauma and patients were similar in both groups. Also, 12 investigation centers will be classified based on annual local average temperatures.
Main collected data Demographics and morphological traits (age, sex, body weight, and height of the victim), the nature and circumstances of the accident (date, time, place), the victim's presentation on mobile intensive care unit (MICU) arrival (trapped or not, seated or lying down, on the ground, unclothed, wet, or covered by a blanket, environmental conditions, clinical factors, and care provided.
Environmental conditions included air (indoors or outdoors) temperature, and rain at the site of the accident as well as mobile intensive care unit temperature.
Clinical factors included: the site and nature of the lesions (fracture, wound, contusion), heart rate, the Revised Trauma Score (RTS) (Glasgow Coma Score (GCS) + systolic blood pressure + respiratory rate), oxygen saturation or oxygen delivery, and tympanic temperature.
Whenever applicable: vascular filling (infusion fluid temperature and volumes), catecholamine and morphine administration, any other drugs (with doses), orotracheal intubation.
Times from the accident to MICU arrival and from MICU arrival to hospital admission.
Statistical analysis Primary endpoint: rate of patients arriving at the hospital with a temperature <35°C. These data will be analyzed by model of multi-level logistic regression to again consider the cluster design of the study. A secondary analysis will enter the model known a priori factors that may affect hypothermia. The parameters corresponding to the secondary objectives will be entered in a model of logistic regression multivariate thereby specifically test their effect on the criteria studied.
Secondary endpoints: Binary secondary endpoints will be analyzed by model of multi-level logistic regression. Quantitative secondary endpoints will be analyzed by mixed model ANCOVA introducing randomness in the center. The variables may be processed before analysis for non-Gaussian distribution. In case of failure of the normalizing transformation, exact procedure may be used.
Number of patients to include The calculation of the sample size was based on our previous study.* The incidence of hypothermia on arrival at the hospital was 14%. By selecting high-risk patients, the investigators expect an incidence of about 20%. The objective is to achieve a reduction of one third of hypothermia (i.e. from 20 to 13 %). Using a two-tailed test at α risk of 0.05 and 1 - beta 0.8, the calculation of required number of patients is 440 per group. Assuming a moderate inflation factor of about 1.35 related to the cluster randomization (our experience shows that intra-cluster correlation coefficients are low) the total number of patients per group will be 600 patients.
A total of N = 1,200 patients for the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trauma Patients
Keywords
Trauma, Prehospital, Hypothermia
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1086 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1: control group
Arm Type
Active Comparator
Arm Description
Classic - current management of trauma patients by French medical teams
Arm Title
2: interventional group
Arm Type
Experimental
Arm Description
Intervention Name : monitoring, treatment, control and prevention of hypothermia
Continuous monitoring of body temperature
Ambulance warming (target : 30°C)
Patient warming with dedicated blanket
Infusion fluid warming (and temperature control)
Intervention Type
Other
Intervention Name(s)
1: control group
Intervention Description
Classic - current management of trauma patients by French medical teams
Intervention Type
Other
Intervention Name(s)
2: interventional group
Intervention Description
Intervention Name : monitoring, treatment, control and prevention of hypothermia
Continuous monitoring of body temperature
Ambulance warming (target : 30°C)
Patient warming with dedicated blanket
Infusion fluid warming (and temperature control)
Primary Outcome Measure Information:
Title
Number of trauma patients arriving alive with a temperature > 35°C (at receiving hospital)
Time Frame
Day0
Secondary Outcome Measure Information:
Title
Survival at hospital discharge
Time Frame
up to 3 months
Title
Length of stay at hospital (days)
Time Frame
up to 3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria :
Patient with trauma (> 18 years)
Pre-hospital management by MICU
Scheduled transfer to a receiving center by a MICU
And at least one of the following criteria :
Ambient temperature on the field < 18°C
Body temperature <35°C on MICU arrival
A Glasgow score < 15 on MICU arrival
Systolic blood pressure < 100 mm Hg on MICU arrival
Exclusion criteria :
- Body temperature <31°C or >38°C
Cardiac arrest before MICU arrival
Bilateral ear bleeding preventing continuous monitoring of tympanic temperature
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frédéric LAPOSTOLLE, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
SAMU 93, AP-HP, Urgences - SAMU 93, Unité Recherche-Enseignement-Qualité, Hôpital Avicenne
City
Bobigny
ZIP/Postal Code
93000
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
22849694
Citation
Lapostolle F, Sebbah JL, Couvreur J, Koch FX, Savary D, Tazarourte K, Egman G, Mzabi L, Galinski M, Adnet F. Risk factors for onset of hypothermia in trauma victims: the HypoTraum study. Crit Care. 2012 Jul 31;16(4):R142. doi: 10.1186/cc11449.
Results Reference
background
Learn more about this trial
Prevention of HYPOthermia in TRAUMa Patients
We'll reach out to this number within 24 hrs