Observational study on complications from severe trauma
Official title: Prospective Cohort of Severe Trauma Patients Hospitalized in West French Intensive Care Units
Run by Nantes University Hospital · NCT02426255 · Data updated 2026-11-12
This study looks at how severe trauma affects patients in the ICU to see what complications arise and how to better manage these serious injuries.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 15 Years and up |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 5 sites (Angers and 4 other locations) |
| Status | Recruiting |
| Started | March 29, 2013 |
| Main results expected | January 2050 |
| Study ends | January 2050 |
| Registry record updated | September 30, 2022 |
| Trial ID | NCT02426255 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients experiencing severe trauma, traumatic brain injury, or hemorrhage.
✕Probably not a fit
Patients who withdraw consent will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational epidemiological study aims to investigate the management and complications associated with severe trauma, including traumatic brain injury and hemorrhage. Data will be collected from ICU patients and analyzed to address pre-defined scientific questions, ultimately aiming to improve the management of these critical conditions. The study will utilize a secured e-database for pseudonymized data collection, ensuring patient confidentiality. Cross audits will be performed to ensure data accuracy and integrity.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for patients suffering from severe trauma.
How similar studies have gone: Other studies have shown success in improving trauma management through observational data collection, making this approach both relevant and tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * severe trauma * and/or traumatic brain injury * and/or hemorrhage Exclusion Criteria: * Consent withdrawal
Where it's running
-
Angers University Hospital
Angers, France Recruiting -
Nantes University Hospital
Nantes, France Recruiting -
Poitiers University Hospital
Poitiers, France Recruiting -
Rennes University Hospital
Rennes, France Recruiting -
Tours University Hospital
Tours, France Recruiting
Study contacts
- Study coordinator: Karim Asehnoune, PhD, MD
- Email: karim.asehnoune@chu-nantes.fr
- Phone: 02 40 08 73 80
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.