跳至主要内容
临床试验/NCT00912561
NCT00912561终止不适用

Effects of Intense Aerobic Exercise on the Cerebrovascular Reserve Capacity in Patients With Hemodynamically Relevant Intra- and Extracranial Stenoses

Gerhard Jan Jungehuelsing2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
50
试验地点
2
主要终点
change of cerebrovascular reserve capacity

研究概览

简要总结

The purpose of this trial is to study the improvement of cerebral hemodynamics in high risk stroke patients with impaired Cerebrovascular Reserve (CVR) due to high grade stenosis of the internal carotid (ICA) or middle cerebral artery (MCA) by Intense Aerobic Exercise (IAEx).

详细描述

The primary objective: Intense aerobic exercise (24/8 weeks) improves CVR > 20% measured by Transcranial Doppler (TCD) in patients with hemodynamic relevant intra- or extracranial stenoses by enhanced cerebral arterio- and angiogenesis.

Secondary objectives:

Intense aerobic exercise (24/8 weeks) leads to:

  • an increase of Endothelial progenitor cell counts (EPCs)
  • qualitative and quantitative changes of endothelial markers and cytokines representing the inflammatory activity of atherosclerosis and neovascularisation
  • an improvement in cognitive performance and quality of life (QoL)
  • changes of the mean vessel size and of cerebral perfusion

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • high-grade stenosis of the intra- or extracranial ICA or the MCA with ipsilateral impairment of the CVR capacity measured by TCD

排除标准

  • continuous physical activity ≥ 60 min/week within the last 3 months
  • cerebral bleeding or ischaemic stroke < 3 months
  • contraindications for spiro-ergometry, IAEx, or MRI

结局指标

主要结局

change of cerebrovascular reserve capacity

时间窗: immediately after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up

次要结局

  • Endothelial Progenitor Cells, cyto- and chemokines(after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up)
  • Neuropsychological Testing/ Quality of life(immediately after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up)

研究者

发起方
Gerhard Jan Jungehuelsing
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Gerhard Jan Jungehuelsing

MD

Charite University, Berlin, Germany

研究点 (2)

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