Dijon Stroke Cohort
Recruiting
Observational Study
CVA, Dijon Registry
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 4,000 (estimated)
- Sponsor
- Centre Hospitalier Universitaire Dijon · Other
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About This Trial
The Dijon Stroke Registry, accredited by the Registry Evaluation Committee, INSERM and Public Health France, has been studying the epidemiology of cerebrovascular accidents (cerebral infarction, intracerebral haemorrhages, meningeal haemorrhages) and transient ischaemic attacks (TIAs) within the city of Dijon since 1985.
As a result of the development of therapies for acute disease, the prognosis…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* patients included in the Dijon Stroke Registry and not opposed to participating
Exclusion Criteria:
* minor patients; opposition to participation
Contacts