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Clinical Trials/JPRN-UMIN000021251
JPRN-UMIN000021251
Completed
未知

The exploratory study for the efficacy and the safety of Hangeshashinto on symptoms of heartburn /belch in the patients with gastroesophageal reflux disease (GERD) - The efficacy of Hangeshasinto on heartburn/belch in the patients with GERD

Osaka Medical College0 sites80 target enrollmentMarch 1, 2016
ConditionsGERD

Overview

Phase
未知
Intervention
Not specified
Conditions
GERD
Sponsor
Osaka Medical College
Enrollment
80
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 1, 2016
End Date
April 30, 2018
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) History of upper GI resection 2\) Confirmed presence of ulcer (excluding scars) or malignant tumor in the upper GI. 3\) Non\-erosive reflux disease (Los Angeles classification, Grade N) 4\) suspected organic hepatic/biliary/pancreatic disorders such as gallstone, hepatitis, and pancreatitis 5\) History of allergic reactions to Kampo medicines 6\)Patients who is taking P\-CAB. 7\) Patients who were administered KAMPO medicine 4 weeks before entry. 8\) receiving or scheduled to receive an agent that is being developed 9\) presence of serious complications (liver, kidney, heart, or blood disease or metabolic disease). 10\) Pregnant or lactating women or those who are planning to conceive during the study period. 11\) considered ineligible to participate by principal investigator or sub\-investigator

Outcomes

Primary Outcomes

Not specified

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