Viewing Study NCT03149393


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Study NCT ID: NCT03149393
Status: UNKNOWN
Last Update Posted: 2020-02-28
First Post: 2017-04-16
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Clinical Study on Post Evaluation After Listing of Qizhi Weitong Granules
Sponsor: Xiyuan Hospital of China Academy of Chinese Medical Sciences
Organization:

Study Overview

Official Title: Clinical Study on Post Evaluation After Listing of Qizhi Weitong Granules
Status: UNKNOWN
Status Verified Date: 2020-02
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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.
Detailed 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 Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: