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临床试验/NCT01363856
NCT01363856Unknown不适用

Center for Stroke Research Berlin (CSB) Prospective Stroke Cohort

Charite University, Berlin, Germany2 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2010年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
750
试验地点
2
主要终点
Combined vascular endpoint composed of stroke, myocardial infarction, and vascular death

研究概览

简要总结

The primary aim of the study is to derive and validate risk scores for vascular endpoints (recurrent stroke, myocardial infarction, and other complications of stroke) and for death following an incident stroke. For this purpose patients with an incident stroke will be followed for 36 months with additional assessments at 12, 24 and 36 months.

详细描述

Risk of vascular disease including stroke, myocardial infarction, and vascular death is high after stroke but there are only few prognostic models for long term risk up to 3 years. About 850 patients with an incident stroke will be followed for 3 years with assessments at baseline and at 3, 12, 24, and 36 months. Factors that have already been reported to be significant predictors of vascular diseases in previous studies as well as new biomarkers (e.g. neuroimaging, blood based biomarkers) identified in this cohort will be considered. The improvement of discrimination including these new variables in the models will be investigated. Several measures of improving predictive properties (e.g. calibration, discrimination, net reclassification) will be used to compare predictive models with different complexity. The model will be validated using the bootstrap method (internal validation) and an independent external sample in cooperation with the Institute for Stroke and Dementia Research, Munich.

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

  • Age ≥18 years
  • Language: German
  • First ever stroke including ischemic stroke, primary intracranial hemorrhage and cerebral venous sinus thrombosis that occurred with stroke onset in the last 7 days
  • Written informed consent by patient prior to study participation
  • Willingness to participate in follow-up

排除标准

  • Prior stroke (definition according to WHO definition)
  • Patients presenting brain tumour or brain metastasis
  • Participation in an intervention- / AMG-study

结局指标

主要结局

Combined vascular endpoint composed of stroke, myocardial infarction, and vascular death

时间窗: 36 months

This evaluation will be based on a structured interview with the patient. In case of positive screening more information will be obtained by hospital or physician.

次要结局

  • Combined vascular endpoint composed of stroke, myocardial infarction, and vascular death(12 months)
  • Course of cognitive function(36 months)
  • Course of depression(36 months)

研究者

申办方类型
Other

研究点 (2)

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