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The exploratory study for the efficacy and the safety of Rikkunshito on symptoms of indigestion in the patients with Functional Heartbur

Not Applicable
Conditions
Functional Heartburn
Registration Number
JPRN-UMIN000029668
Lead Sponsor
ippon Medical School Graduate School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

1)Patients diagnosed with Eosinophilic esophagitis(EoE) 2)Patients diagnosed with Esophageal Motility disorders by High-Resolution manometry. 3)Patients who had 50% or more of Symptom Index by 24-hour Esophageal Impedance and PH monitoring. 4)Patients diagnosed with Reflux esophagitis(RE)(Los Angeles classification,>=Grade A)by upper endoscopy. 5)History of upper GI resection 6)Confirmed presence of ulcer (excluding scars) or malignant tumor in the upper GI. 7)Suspected organic hepatic/biliary/pancreatic disorders such as gallstone, hepatitis, and pancreatitis 8)History of allergic reactions to Kampo medicines. 9)Patients who were administered KAMPO medicine 4 weeks before entry. 10)Receiving or scheduled to receive an agent that is being developed. 11)Presence of serious complications (liver, kidney, heart, or blood disease or metabolic disease). 12)Pregnant or lactating women or those who are planning to conceive during the study period. 13)Considered ineligible to participate by principal investigator or sub-investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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