Post Traumatic Critical Complications: a Prospective Cohort Study (ATLANREA)
NCT ID: NCT02426255
Last Updated: 2022-09-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
5000 participants
OBSERVATIONAL
2013-03-29
2050-01-31
Brief Summary
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Detailed Description
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Cross audit will be performed to check data.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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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
Collection of medical data from ICU patients
A code will be applied to each patient included. Medical data such as demography, Simplified Acute Physiological Score II (SAPS II), Sequential Organ Failure Assessment (SOFA), procedures and complications during ICU stay will be collected.
Interventions
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Collection of medical data from ICU patients
A code will be applied to each patient included. Medical data such as demography, Simplified Acute Physiological Score II (SAPS II), Sequential Organ Failure Assessment (SOFA), procedures and complications during ICU stay will be collected.
Eligibility Criteria
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Inclusion Criteria
* and/or traumatic brain injury
* and/or hemorrhage
Exclusion Criteria
15 Years
ALL
No
Sponsors
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Nantes University Hospital
OTHER
Responsible Party
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Principal Investigators
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Karim ASEHNOUNE, PhD, MD
Role: STUDY_CHAIR
Locations
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Angers University Hospital
Angers, , France
Nantes University Hospital
Nantes, , France
Poitiers University Hospital
Poitiers, , France
Rennes University Hospital
Rennes, , France
Tours University Hospital
Tours, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RC12_0207 cohorte fiche 2
Identifier Type: -
Identifier Source: org_study_id
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