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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00912561
Other study ID # CCBF-Exercise
Secondary ID EA4/106/08
Status Terminated
Phase N/A
First received June 2, 2009
Last updated February 20, 2012
Start date June 2009
Est. completion date December 2012

Study information

Verified date February 2012
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

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).


Description:

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


Recruitment information / eligibility

Status Terminated
Enrollment 50
Est. completion date December 2012
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

- 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

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Intense aerobic exercise
3 Units (of at least 30 minutes) of intense aerobic exercise per week for 8 weeks

Locations

Country Name City State
Germany Centre for Stroke Research Berlin, Neurology, Charité Campus Benjamin Franklin Berlin

Sponsors (2)

Lead Sponsor Collaborator
Gerhard Jan Jungehuelsing German Federal Ministry of Education and Research

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of cerebrovascular reserve capacity immediately after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up No
Secondary Endothelial Progenitor Cells, cyto- and chemokines after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up No
Secondary Neuropsychological Testing/ Quality of life immediately after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up No
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