Post Traumatic Critical Complications: a Prospective Cohort Study (ATLANREA)
- Conditions
- Severe Trauma (With or Without Traumatic Brain Injury)
- Interventions
- Other: Collection of medical data from ICU patients
- Registration Number
- NCT02426255
- Lead Sponsor
- Nantes University Hospital
- Brief Summary
The purpose of this observational epidemiological study is to investigate the management and the complications associated with severe trauma. Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.
- Detailed Description
Pseudonymized data will be collected by study coordinators in a secured e-database.
Cross audit will be performed to check data.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 5000
- severe trauma
- and/or traumatic brain injury
- and/or hemorrhage
- Consent withdrawal
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description ICU patients Collection of medical data from ICU patients Patients with severe trauma (with or without brain injury) or Patients with hemorrhagic shock Data concerning the ICU stay will be collected for these patients
- Primary Outcome Measures
Name Time Method in ICU stay complications Within the 28 first days after ICU admission date Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors) Bleeding, hemorrhage Intra-cranial hypertension, brain ischemia Mechanical ventilation weaning, extubation failure
- Secondary Outcome Measures
Name Time Method Duration of mechanical ventilation in ICU (up to 90 days) ICU length of stay in ICU (up to 90 days)
Trial Locations
- Locations (5)
Nantes University Hospital
🇫🇷Nantes, France
Poitiers University Hospital
🇫🇷Poitiers, France
Rennes University Hospital
🇫🇷Rennes, France
Angers University Hospital
🇫🇷Angers, France
Tours University Hospital
🇫🇷Tours, France