Clinical Trials Directory

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

TypeNameDescription
OTHERQuestionnaire and semi-structured interviewquestionnaire 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.