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Dijon Stroke Cohort (DISCO)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Enrolling

Conditions

CVA, Dijon Registry

Treatments

Other: Questionnaire and semi-structured interview

Study type

Observational

Funder types

Other

Identifiers

NCT04489199
BEJOT 2020

Details and patient eligibility

About

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.

Enrollment

4,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients included in the Dijon Stroke Registry and not opposed to participating

Exclusion criteria

  • minor patients; opposition to participation

Trial design

4,000 participants in 1 patient group

Stroke patient
Description:
Patient included in the Dijon Stroke Registry.
Treatment:
Other: Questionnaire and semi-structured interview

Trial contacts and locations

1

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Central trial contact

Yannick BEJOT

Data sourced from clinicaltrials.gov

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