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Clinical Trial Summary

The main objective of the study is to compare the effectiveness of moxifloxacin triple therapy with levofloxacin-based sequential therapy in terms of eradication rate, safety, and patient compliance.


Clinical Trial Description

Patients who were confirmed to be positive for Helicobacter Pylori infection were randomly assigned to the eradication treatments. At four weeks after completion of eradication therapy, H. pylori tests were performed with a Stool antigen test. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05863858
Study type Interventional
Source University of Karachi
Contact
Status Completed
Phase Phase 3
Start date June 1, 2020
Completion date June 8, 2022

See also
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