Clinical Study on Post Evaluation After Listing of Qizhi Weitong Granules

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

This study is a randomized, double blind, double dummy, multicenter, parallel controlled clinical trial, the investigators objective is to evaluate the efficacy and safety of Qizhi Weitong granules in the treatment of functional dyspepsia. The experiment will be carried out in 8 sub centers at the same time, and the investigators estimated that there will be 384 cases of income, including the experimental group and the control group (n = 192), and the investigators choose mosapride citrate tablets for drug control. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03149393
Study type	Interventional
Source	Xiyuan Hospital of China Academy of Chinese Medical Sciences
Contact	Wang F yun, PhD
Phone	13522657731
Email	wfy811@163.com
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	February 1, 2017
Completion date	December 31, 2020

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