Trial of Chinese Prescription Shugan Decoction on Irritable Bowel Syndrome（Diarrhea Type）
NCT ID: NCT00948870
Last Updated: 2013-03-07
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
2011-09-30
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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Shugan Decoction
Shugan decoction
Decoction ,two times a day,one bag of decoction one time
low does of Shugan decoction
Shugan decoction
Decoction ,two times a day,one bag of decoction one time
Interventions
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Shugan decoction
Decoction ,two times a day,one bag of decoction one time
Eligibility Criteria
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Inclusion Criteria
* Male of female patients between 18-65 years old
* Written informed consent
Exclusion Criteria
* Diarrhea-type of irritable bowel syndrome combine with intestinal disease
* 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-002
Identifier Type: -
Identifier Source: org_study_id
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