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Clinical Trial Summary

The purpose of this study is to evaluate the safety and validity of Aolanti Weipang Tablets in Patients with Postprandial Discomfort Syndrome of Functional Dyspepsia


Clinical Trial Description

This is a multi-center, randomized, double blind, placebo-controlled phase Ⅱc study to evaluate the safety and validity of Aolanti Weipang Tablets in patients with postprandial discomfort syndrome of Functional Dyspepsia(FD). This study will consecutive about 12 weeks, including 2 weeks of screening, 1 week of blank run-in, 1 week of placebo run-in, 4 weeks of double blind treatment and 4 weeks of observation after treatment. The subjects will be randomly given orally Aolanti Weikang Tablets or placebo tablets at a 1:1 ratio three times a day(tid) with 3 tablets one time for the treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03971383
Study type Interventional
Source Jiangxi Qingfeng Pharmaceutical Co. Ltd.
Contact Qinsheng Zhang
Phone +86-18036618691
Email zhangqinsheng@sh-qingfeng.net
Status Not yet recruiting
Phase Phase 2
Start date June 10, 2019
Completion date May 3, 2021

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