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| Sponsored by: |
Far Eastern Memorial Hospital |
| Information provided by: | Far Eastern Memorial Hospital |
| ClinicalTrials.gov Identifier: | NCT00422474 |
Purpose
After acute stroke, baroreflex sensitivity (BRS) is impaired. This impaired acute stage BRS has been reported to be predictive of worsen outcome years after stroke in general. However, it is not very clear if the impaired acute stroke BRS would actually persist months after the acute stage. It is also not clear that such change, if any, would correlate with the functional outcome or prognosis after stroke.
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.
| Condition |
|
Cerebrovascular Accident Baroreflexes Autonomic Nervous System Diseases |
| MedlinePlus related topics: | Autonomic Nervous System Disorders Neurologic Diseases |
| Study Type: | Observational |
| Study Design: | Prospective |
| Official Title: | Noninvasive Study of the Time Course of Baroreflex Sensitivity 6-Month After Acute Ischemic Stroke and the Relation of Its Changes With Post Stroke Prognosis |
Eligibility
| Ages Eligible for Study: | 50 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Siupak Lee, M.D. | siupakmd@ms1.hinet.net |
| Taiwan, Taipei County | |||||
| Far Eastern Memorial Hospital | Recruiting | ||||
| Panchiao City, Taipei County, Taiwan, 220 | |||||
| Contact: Siupak Lee, M.D. siupakmd@ms1.hinet.net | |||||
| Principal Investigator: Siupak Lee, M.D. | |||||
| Sub-Investigator: Lung Chan, M.D. | |||||
| Sub-Investigator: Dong-feng Yeih, M.D. | |||||
| Far Eastern Memorial Hospital |
| Principal Investigator: | Siupak Lee, M.D. | Far Eastern Memorial Hospital |
More Information
| Responsible Party: | Far Eastern Memorial Hospital ( Dr. Siupak Lee ) |
| Study ID Numbers: | FEMH-95-C-012 |
| First Received: | January 14, 2007 |
| Last Updated: | July 8, 2008 |
| ClinicalTrials.gov Identifier: | NCT00422474 |
| Health Authority: | Taiwan: Department of Health |
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