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NCT Number: NCT04489199

Dijon Stroke Cohort

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.

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Key information

Conditions

CVA, Dijon Registry Brain Diseases Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Nervous System Diseases Stroke Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • minor patients; opposition to participation

Treatment and study plan

Questionnaire and semi-structured interview

Other

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

Primary outcomes

  1. Death rate

    Time frame: Trough study completion, an average of 10 years

  2. Disability rate

    Time frame: Trough study completion, an average of 10 years

  3. Quality of Life Questionnaire

    Time frame: Trough study completion, an average of 10 years

  4. Neuropsychological questionnaire

    Time frame: Trough study completion, an average of 10 years

Study contacts

Contact information is provided by the study sponsor or research team.

Yannick BEJOT

CONTACT

[email protected]

03.80.29.37.53 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Dijon

Other

Registry information

Acronym: DISCO

Important dates

Study start
2021
Primary completion
2040
Study completion
2040
First posted
Jul 28, 2020
Registry last updated
Feb 20, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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