Efficacy of Vonoprazan-based Rescue Therapy for H. Pylori Eradication

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorNational Taiwan University Hospital

About this trial

1. This study aims to compare the efficacy of empirical vonoprazan-based therapy versus susceptibility-guided vonoprazan-based therapy for third-line eradication of H. pylori. 2. We also plan to explore the impact of eradication therapy on gut microbiota, fecal antibiotic resistance, and metabolic parameters before and after treatment.

Eligibility criteria

Qualifiers

Helicobacter pylori infected individuals who have failed at least two previous eradication therapies.

Willing to undergo third-line eradication therapy.

Subjects must be 20 years of age or older.

Disqualifiers

History of gastrectomy.

Individuals unsuitable for the study medication, such as those with a history of allergy or severe adverse reactions to the study drugs, quinolone or fluoroquinolone antibiotics, or women who are pregnant or breastfeeding.

Presence of severe acute or chronic diseases such as renal failure, liver cirrhosis, incurable malignant tumors, or a history of aortic aneurysm or dissection.

Patients with chronic hepatitis (AST or ALT > 100 U/L).

Trial design

Treatments tested in this trial

  • Vonoprazan based ET
  • Vonoprazan based SGT

Treatment groups

220 Participants
are divided into 2 treatment groups