Trials / Recruiting
RecruitingNCT04489199
Dijon Stroke Cohort
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 4,000 (estimated)
- Sponsor
- Centre Hospitalier Universitaire Dijon · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Questionnaire 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 |
Timeline
- Start date
- 2021-01-01
- Primary completion
- 2040-01-01
- Completion
- 2040-01-01
- First posted
- 2020-07-28
- Last updated
- 2024-02-20
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT04489199. Inclusion in this directory is not an endorsement.