CVA, Dijon Registry
Conditions
Brief summary
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 of patients has improved over time. Thus, the number of stroke survivors has increased by 90% between the 1980s and today. This raises new issues: risk of vascular recurrence, drug iatrogeny, and functional impact of stroke for motor, cognitive or thymic function. In the absence of available data in France, the investigators wish to set up an extended cohort follow-up of patients in order to study their long-term prognosis and to study the impact of future therapies on the evolutionary course of the disease.
Interventions
OTHERQuestionnaire and semi-structured interview
questionnaire submitted by telephone 3 months, 6 months, 1 year, 5 years, and 10 years after the stroke/TIA. interview duration 20 to 40 minutes
Sponsors
Centre Hospitalier Universitaire Dijon
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* patients included in the Dijon Stroke Registry and not opposed to participating
Exclusion criteria
* minor patients; opposition to participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Death rate | Trough study completion, an average of 10 years |
| Disability rate | Trough study completion, an average of 10 years |
| Quality of Life Questionnaire | Trough study completion, an average of 10 years |
| Neuropsychological questionnaire | Trough study completion, an average of 10 years |
Countries
France
Contacts
Primary ContactYannick BEJOT
Outcome results
None listed