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Clinical Trials/JPRN-UMIN000029668
JPRN-UMIN000029668
Not yet recruiting
未知

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

ippon Medical School Graduate School of Medicine0 sites20 target enrollmentOctober 24, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Functional Heartburn
Sponsor
ippon Medical School Graduate School of Medicine
Enrollment
20
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 24, 2017
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
ippon Medical School Graduate School of Medicine

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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