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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COMPLETED
NA
200 participants
INTERVENTIONAL
2009-08-31
2011-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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bascial prescription
Decoction ,two times a day,one bag of decoction one time
bascial prescription plus or minus herbs depend on symptoms
Decoction ,two times a day
low does of bascial decoction
Decoction ,two times a day, one bag decoction of one time
bascial prescription plus or minus herbs depend on symptoms
Decoction ,two times a day
Interventions
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bascial prescription plus or minus herbs depend on symptoms
Decoction ,two times a day
Eligibility Criteria
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Inclusion Criteria
* Male of female patients between 18-65 years old
* Written informed consent
Exclusion Criteria
* Combined with severe heart, gallbladder, kidney, endocrine system, hemopoietic system or nervous system disease.
* Pregnancy or breast feeding women, or unwilling to have contraception.
18 Years
65 Years
ALL
No
Sponsors
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Shanghai University of Traditional Chinese Medicine
OTHER
Responsible Party
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Principal Investigators
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Xie Jianqun, Phd
Role: STUDY_DIRECTOR
Shanghai University of Chinese Medicine
Locations
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Longhua hospital
Shanghai, Shanghai Municipality, China
Countries
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Other Identifiers
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SHTCM-003
Identifier Type: -
Identifier Source: org_study_id
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