Effectiveness and Safety of Rhubarb for the Treatment of Patients Who Have Suffered From a Stroke
NCT ID: NCT00789269
Last Updated: 2010-05-28
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
PHASE2
100 participants
INTERVENTIONAL
2009-01-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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1
rhubarb
rhubarb
14 days of rhubarb
2
placebo
14 days of placebo
Interventions
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rhubarb
14 days of rhubarb
placebo
14 days of placebo
Eligibility Criteria
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Inclusion Criteria
* Have no pneumonia according to modified criteria of the U.S. Centers for Disease Control and Prevention (CDC)
* Consistent with the Constipation of Phlegm-Heat Accumulation type by Traditional Chinese Medicine (TCM) standard
* Patients or their representatives voluntarily take part in this study and signed the informed consent
Exclusion Criteria
* Transient ischemic attack(TIA)
* Proven cerebral embolism caused by tumor, Brain Trauma, cerebral parasitic disease, dysbolismus, fibrillation atrial resulted from rheumatic heart disease, coronary heart disease, and other heart diseases
* Clinical signs of infection on admission
* Pregnant or breast-feeding
* Allergic to rhubarb
* Preceding or ongoing antibiotic therapy within the last 24 h
* Participation in another interventional trial
* Immunosuppressant treatment within the last 30 days
* Combining severe clinical conditions such as liver, kidney, Hematopoietic System, endocrine system or psychological diseases
18 Years
ALL
No
Sponsors
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Fudan University
OTHER
Responsible Party
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TCM department, Zhongshan hospital, Fudan University
Locations
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Department of Integrative Medicine, Zhongshan hospital, Fudan University
Shanghai, Shanghai Municipality, China
Countries
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Other Identifiers
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rhubarb ischemia
Identifier Type: -
Identifier Source: org_study_id