Observational study on complications of non-traumatic brain injuries
Official title: Prospective Cohort of Patients Hospitalized in West French Intensive Care Units.
Run by Nantes University Hospital · NCT02714387 · Data updated 2026-11-12
This study looks at how non-traumatic brain injuries are managed and what complications can arise for people dealing with these conditions.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 15 Years and up |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 6 sites (Angers and 5 other locations) |
| Status | Recruiting |
| Started | February 2013 |
| Main results expected | January 2050 |
| Study ends | January 2050 |
| Registry record updated | September 30, 2022 |
| Trial ID | NCT02714387 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals diagnosed with non-traumatic neuro-vascular diseases.
✕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 non-traumatic neuro-vascular diseases, specifically focusing on non-traumatic acute brain injury. Data will be collected anonymously by study coordinators and stored in a secured electronic database. The study will analyze this data to address pre-defined scientific questions and enhance the management of these conditions. Cross audits will be conducted to ensure data integrity and reliability.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for patients with non-traumatic acute brain injuries.
How similar studies have gone: Other studies focusing on similar non-traumatic brain injuries have shown promise in improving patient outcomes, indicating that this approach is supported by prior research.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Non Traumatic Neuro-Vascular Diseases Exclusion Criteria: * Consent withdrawal
Where it's running
-
Angers University Hospital
Angers, France Recruiting -
CHU de Brest La Cavale Blanche
Brest, 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.