Trial of Chinese Prescription Shugan Decoction on Irritable Bowel Syndrome（Diarrhea Type）

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00948870

Enrollment

200

Registered

2009-07-29

Start date

2009-08-31

Completion date

2011-09-30

Last updated

2013-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritable Bowel Syndrome, Traditional Chinese Medicine

Keywords

alternative medicine

Brief summary

The purpose of this study is to evaluate the efficacy and safety of the Chinese prescription Shugan decoction on irritable bowel syndrome（diarrhea type）.

Interventions

DRUGShugan decoction

Decoction ,two times a day,one bag of decoction one time

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Inclusion criteria

* Clinical diagnosis of irritable bowel syndrome（diarrhea type） * Male of female patients between 18-65 years old * Written informed consent

Exclusion criteria

* Discrepancy of irritable bowel syndrome * 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.

Design outcomes

Primary

Measure	Time frame
Symptoms and conditions of tongue and pulse	4 weeks

Secondary

Measure	Time frame
Indicates of liver and renal function	4 weeks

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026