Viewing Study NCT05388890



Ignite Creation Date: 2024-05-06 @ 5:40 PM
Last Modification Date: 2024-10-26 @ 2:33 PM
Study NCT ID: NCT05388890
Status: RECRUITING
Last Update Posted: 2023-09-05
First Post: 2022-05-19

Brief Title: Treatment of Atrophic Gastritis After HP Eradication With Modified Liujunzi Decoction Based on Syndrome Differentiation
Sponsor: Peking University First Hospital
Organization: Peking University First Hospital

Study Overview

Official Title: Clinical Study on the Efficacy of Modified Liujunzi Prescription on the Treatment of Atrophic Gastritis After HP Eradication
Status: RECRUITING
Status Verified Date: 2023-08
Last Known Status: None
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 is an observational cohort study of clinical efficacy studyThe purpose of this topic is to evaluate the efficacy and safety of Modified Liujunzi Decoction based on syndrome differentiation in patients with chronic atrophic gastritisCAG after HP eradicationTaking Modified Liujunzi Decoction as the observation group and Weifuchun routine treatment as the control group so as to provide evidence for the treatment of CAG and reduce the risk of gastric cancer A total of 284 patients were included The curative efficacy symptom score and adverse events will be recorded and analyzed
Detailed Description: None

Study Oversight

Has Oversight DMC: None
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?: None