Long-term follow-up of stroke patients in Dijon
Official title: Dijon Stroke Cohort
Run by Centre Hospitalier Universitaire Dijon · NCT04489199 · Data updated 2026-11-12
This study looks at how stroke survivors in Dijon are doing over the long term to see what challenges they face and how treatments affect their health.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 4000 (estimated) |
| Sponsor | Centre Hospitalier Universitaire Dijon Academic / other |
| Locations | 1 site (Dijon) |
| Status | Recruiting |
| Started | January 1, 2021 |
| Main results expected | January 2040 |
| Study ends | January 2040 |
| Registry record updated | February 20, 2024 |
| Trial ID | NCT04489199 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients who have been included in the Dijon Stroke Registry and consent to participate.
✕Probably not a fit
Patients who are minors or oppose participation 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
The Dijon Stroke Cohort aims to investigate the long-term prognosis of patients who have experienced cerebrovascular accidents, including strokes and transient ischemic attacks, within the city of Dijon. Since 1985, the study has been collecting data on the epidemiology of these conditions, focusing on the evolving challenges faced by stroke survivors, such as the risk of recurrence and the impact of therapies. Participants will be assessed through questionnaires and semi-structured interviews to gather comprehensive data on their health outcomes and the effects of future treatments.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the long-term management and rehabilitation of stroke survivors, potentially improving their quality of life.
How similar studies have gone: Other studies have shown success in similar observational approaches to understanding long-term outcomes in stroke patients, indicating the potential value of this research.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients included in the Dijon Stroke Registry and not opposed to participating Exclusion Criteria: * minor patients; opposition to participation
Where it's running
-
Chu Dijon Bourgogne
Dijon, France Recruiting
Study contacts
- Study coordinator: Yannick BEJOT
- Email: yannick.bejo@chu-dijon.fr
- Phone: 03.80.29.37.53
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.