Efficacies of Bismuth-amoxicillin-vonoprazan Triple Therapy and Bismuth Quadruple Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKaohsiung Medical University

About this trial

(1) To compare the efficacy and safety of a 14-day bismuth-amoxicillin-vonoprazan triple therapy versus a 14-day bismuth-based quadruple therapy as first-line treatments for H. pylori infection, and (2) To investigate the influence of H. pylori antibiotic resistance, along with host CYP3A4, CYP2C19, and IL-1B -511 genotypes, on the eradication efficacy of H. pylori therapies.

Eligibility criteria

Qualifiers

Subjects with Helicobacter pylori infection

Disqualifiers

Subjects with known hypersensitivity to the study drug.

Subjects with a history of gastric surgery.

Subjects with severe liver cirrhosis or uremia.

Subjects with a history of malignancy within the past five years.

Trial design

Treatments tested in this trial

  • vonoprazan, tripotassium dicitrate bismuthate, amoxicilline
  • rabeprazole, tripotassium dicitrate bismuthate, tetracycline, metronidazole

Treatment groups

552 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Kaohsiung Medical University

Lead sponsor

Kaohsiung Veterans General Hospital.

Collaborator