Prognostic Significance of the Baroreflex Sensitivity Changes After Acute Ischemic Stroke
NCT ID: NCT00422474
Last Updated: 2008-07-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2007-01-31
Brief Summary
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The trial is to investigate the longitudinal time course of BRS after ischemic stroke up to the 6th month post stroke and to see if there is any correlation of the changes in BRS with the functional outcome parameters using NIHSS and mRS scores throughout this period.
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* 50-80 years old
* Must have either brain CT or brain MRI done
Exclusion Criteria
* Patient could not cooperate
* Unstable vital sign
* Atrial fibrillation
* Transient ischemic attack patient
* Diabetic patient
* Impaired renal function (Cr \> 2.26 mg/dl)
* Unstable angina, acute myocardiac infarction, cardiomyopathy patients
* Patient who has known autonomic dysfunction
50 Years
80 Years
ALL
No
Sponsors
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Far Eastern Memorial Hospital
OTHER
Responsible Party
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Far Eastern Memorial Hospital
Principal Investigators
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Siupak Lee, M.D.
Role: PRINCIPAL_INVESTIGATOR
Far Eastern Memorial Hospital
Locations
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Far Eastern Memorial Hospital
Banqiao District, Taipei, Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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FEMH-95-C-012
Identifier Type: -
Identifier Source: org_study_id
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