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

Shanghai University of Traditional Chinese Medicine200 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

200

Conditions

Irritable Bowel Syndrome Traditional Chinese Medicine

Interventions

Shugan decoctionDRUG

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

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

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.

Locations (1)

Longhua hospital

Shanghai, Shanghai Municipality, China

Outcomes

Primary Outcomes

Symptoms and conditions of tongue and pulse

Time frame: 4 weeks

Secondary Outcomes

Indicates of liver and renal function

Time frame: 4 weeks

Data from ClinicalTrials.gov

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