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Randomized controlled trial to determine the efficacy and safety of daikenchuto for abdominal pain and bloating sensation of IBS

Not Applicable
Conditions
Irritable bowel syndrome
Registration Number
JPRN-UMIN000001797
Lead Sponsor
TJ-100 IBS study group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients who have bowel move disturbance by organic lesion such as IBD(UC and crohn disease etc.) and cancer. 2) Patients suspected of obstruction in stomach and intestines, and with a history of total gastric resection or bowel resection but not apendicitis 3) Patients with hypercalcemia, calculus in the kidney and dysfunction of kidneys. 4) Patients who are taking cardiac glycoside and tetracyclines antibiotics. 5) Patients who took antibiotics at least 2 month prior to observation period 6) Patients with serious complications (liver, kidney, heart, lung, circulatory, or metabolic disorder) 7) Patients with a history of drug allergy 8) Patients who are nursing, pregnant or considering conception 9) Patients who are taking Kampo medicine. 10) Others, including patients who are unfit for the study as determined by the research director or others

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
IBS-QOL-J
Secondary Outcome Measures
NameTimeMethod
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