Observational study on complications of non-traumatic brain injuries
Prospective Cohort of Patients Hospitalized in West French Intensive Care Units.
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 |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 15 Years and up |
| Sex | All |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 6 sites (Angers and 5 other locations) |
| Trial ID | NCT02714387 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with non-traumatic neuro-vascular diseases.
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 with non-traumatic acute brain injuries.
How similar studies have performed: 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.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Non Traumatic Neuro-Vascular Diseases Exclusion Criteria: * Consent withdrawal
Where this trial is running
Angers and 5 other locations
- 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
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.