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Clinical Study on the Efficacy of Modified Liujunzi Prescription on the Treatment of Atrophic Gastritis After HP Eradication
This is an observational cohort study of clinical efficacy study.The purpose of this topic is to evaluate the efficacy and safety of Modified Liujunzi Decoction based on syndrome differentiation in patients with chronic atrophic gastritis(CAG) after HP eradication.Taking 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.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Peking University First Hospital
Beijing, Beijing Municipality, China
Start Date
August 2, 2022
Primary Completion Date
December 31, 2024
Completion Date
December 31, 2025
Last Updated
September 5, 2023
286
ESTIMATED participants
MLD
DRUG
WFC
DRUG
Lead Sponsor
Peking University First Hospital
NCT03261934
NCT05493124
NCT03314038
Data Source & Attribution
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