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Clinical Trial Summary

- This clinical trial is conducted as a double-blind, randomized, and active drug control clinical trial. If the screening results determine that the selection/exclusion criteria are met, the clinical trial drugs are randomly assigned at a 1:1 ratio of the Pexuprazan 40 mg and the Lansoprazole 15 mg dose group and taken for 4 weeks. - Gastritis symptoms are evaluated four weeks after baseline (Visit1) and clinical drug administration (Visit2), and if it is determined that gastritis is necessary according to the medical team's judgment due to gastrointestinal symptoms during the study participation period, endoscopy is performed to check whether gastritis occurs.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05946135
Study type Interventional
Source Yonsei University
Contact Ji Ye Jung
Phone 82-2-2228-0430
Email stopyes@yuhs.ac
Status Not yet recruiting
Phase Phase 4
Start date July 2023
Completion date December 31, 2024