Observational study on complications from severe trauma
Prospective Cohort of Severe Trauma Patients Hospitalized in West French Intensive Care Units
Nantes University Hospital · NCT02426255
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 |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 15 Years and up |
| Sex | All |
| Sponsor | Nantes University Hospital (other) |
| Locations | 5 sites (Angers and 4 other locations) |
| Trial ID | NCT02426255 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are patients experiencing severe trauma, traumatic brain injury, or hemorrhage.
Not a fit: Patients who withdraw consent will not benefit from this study.
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 performed: Other studies have shown success in improving trauma management through observational data collection, making this approach both relevant and tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * severe trauma * and/or traumatic brain injury * and/or hemorrhage Exclusion Criteria: * Consent withdrawal
Where this trial is running
Angers and 4 other locations
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Severe Trauma, Severe trauma, traumatic Brain injury, Hemorrhage