- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04489199
Dijon Stroke Cohort (DISCO)
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Yannick BEJOT
- Phone Number: +33 03.80.29.37.53
- Email: yannick.bejo@chu-dijon.fr
Study Locations
-
-
-
Dijon, France, 21000
- Recruiting
- Chu Dijon Bourgogne
-
Contact:
- Yannick BEJOT
- Phone Number: +33 03.80.29.37.53
- Email: yannick.bejo@chu-dijon.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients included in the Dijon Stroke Registry and not opposed to participating
Exclusion Criteria:
- minor patients; opposition to participation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Stroke patient
Patient included in the Dijon Stroke Registry.
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Death rate
Time Frame: Trough study completion, an average of 10 years
|
Trough study completion, an average of 10 years
|
Disability rate
Time Frame: Trough study completion, an average of 10 years
|
Trough study completion, an average of 10 years
|
Quality of Life Questionnaire
Time Frame: Trough study completion, an average of 10 years
|
Trough study completion, an average of 10 years
|
Neuropsychological questionnaire
Time Frame: Trough study completion, an average of 10 years
|
Trough study completion, an average of 10 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- BEJOT 2020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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