Phase Ⅱc Sutdy of Aolanti Weikang Tablets in FD PDS Patients

Status Not yet recruiting

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

Clinical Trial Details

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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