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Study identifier: NCT07576959 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Bismuth Add-on to Dual Therapy for Helicobacter Pylori Eradication

Condition: HELICOBACTER PYLORI INFECTIONS  ·  Sponsor: National Taiwan University Hospital

PhasePhase 3
Planned participants990
Who can joinAll sexes, 20 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to compare the efficacy and safety of a bismuth-supplemented 14-day vonoprazan-based dual therapy ( triple therapy) versus a 14-day vonoprazan-based dual therapy without bismuth for first-line H. pylori eradication. Furthermore, the investigators will investigate the impact of these eradication regimens on the gut microbiota, the development of antibiotic resistance, and changes in metabolic syndrome indicators pre- and post-treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Mei-Jyh Chen, MD, PhD  ·  886-2-23123456 Ext. 265427  ·  migichen@ntuh.gov.tw

Always discuss trial participation with your own doctor first.

Locations (1)

National Taiwan University HospitalTaipei, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT07576959