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Clinical Trial Summary

The main aim of the study is to review treatment therapies in people with Helicobacter pylori (H. pylori) infections in standard hospital settings in China. In this study, the study doctors will review medical records of participants who have had H. pylori infections any time from 1st January 2019 to 31st December 2021. This study is about collecting existing data only; participants are not treated and do not need to visit a study doctor during this study.


Clinical Trial Description

This is a non-interventional, retrospective cohort study of participants who have evidence of H. pylori infection using pre-existing electronic medical record data in China. This study will evaluate the distribution of methods of eradication therapy among participants who received medications that were used in the eradication therapy for H. pylori infection. Retrospective de-identified participant-level data will be collected primarily from hospitals in China between 1st January 2019 to 31st December 2021. The extracted electronic medical record dataset will include patient demographic information, visit information, diagnosis information, treatment information, and cost information (if available). All the participants will be assigned to a single observational cohort: • Participants with H. pylori This multi-center study will be conducted in China. The overall study duration will be approximately 54 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05073367
Study type Observational
Source Takeda
Contact
Status Completed
Phase
Start date September 21, 2022
Completion date April 12, 2023

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