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临床试验/NCT04489199
NCT04489199招募中不适用

Dijon Stroke Cohort

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 4,000 人开始时间: 2021年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
4,000
试验地点
1
主要终点
Disability rate

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • minor patients; opposition to participation

结局指标

主要结局

Disability rate

时间窗: Trough study completion, an average of 10 years

Quality of Life Questionnaire

时间窗: Trough study completion, an average of 10 years

Death rate

时间窗: Trough study completion, an average of 10 years

Neuropsychological questionnaire

时间窗: Trough study completion, an average of 10 years

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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