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The Efficacy and Safety of "BST104" (Lonicera Flos Extract) in Mild to Moderate Functional Dyspepsia Subjects

Irritable Bowel Syndrome Clinical Trial

Official title:
A Single-center, Randomized, Double-blind, Placebo-controlled, Intervention Study for the Efficacy and Safety of "BST104" (Lonicera Flos Extract) in Mild to Moderate Functional Dyspepsia Subjects

Clinical Trial Summary

This study was conducted to prove the efficacy of BST-104 in patients with mild to moderate FD.

Clinical Trial Description

In this single center, double-blind, randomized clinical trial, patients diagnosed with FD using Rome III criteria were allocated to either test group (300 mg of BST-104, containing 175 mg of Flos Lonicera extracts, twice daily) or placebo group (300 mg placebo, twice daily). Male and female patients > 19 years of age who had mild to moderate FD were eligible. They had baseline endoscopic screening, and patients without active lesions (peptic ulcer disease or gastric erosions) were enrolled. Written informed consent was obtained from all participants. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04008901
Study type Interventional
Source Seoul National University Bundang Hospital
Contact
Status Completed
Phase Phase 3
Start date February 13, 2017
Completion date November 8, 2018
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