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.
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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

Yannick BEJOT

03.80.29.37.53

yannick.bejo@chu-dijon.fr

CONTACT