Dijon Stroke Cohort

Recruiting

• Conditions: CVA, Dijon Registry
• Interventions: Other: Questionnaire and semi-structured interview

• Registration Number: NCT04489199
• Lead Sponsor: Centre Hospitalier Universitaire Dijon

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-07-16
• Study First Submitted QC: 2020-07-27
• Study First Posted: 2020-07-28
• Study Start: 2021-01-01
• Status Verified: 2024-02
• Last Update Submitted: 2024-02-16
• Last Update Posted: 2024-02-20
• Primary Completion: 2040-01
• Study Completion: 2040-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 4000

Inclusion Criteria

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

Exclusion Criteria

• minor patients; opposition to participation

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Stroke patient	Questionnaire and semi-structured interview	Patient included in the Dijon Stroke Registry.

Primary Outcome Measures

Name	Time	Method
Disability rate	Trough study completion, an average of 10 years
Quality of Life Questionnaire	Trough study completion, an average of 10 years
Death rate	Trough study completion, an average of 10 years
Neuropsychological questionnaire	Trough study completion, an average of 10 years

Trial Locations

Locations (1)

Chu Dijon Bourgogne; 🇫🇷 Dijon, France