About this trial
This study aims to evaluate the efficacy of vonoprazan combined with different antibiotics in dual therapy for Helicobacter pylori eradication treatment. Newly infected patients were randomly assigned to four groups: amoxicillin dual therapy, tetracycline dual therapy, minocycline dual therapy, and bismuth quadruple therapy. At the follow - up visit in the 6th week, urea breath test, rapid urease test, or Helicobacter pylori fecal antigen test will be conducted to confirm eradication.
Eligibility criteria
Qualifiers
Aged 18 - 70 years, regardless of gender;
Patients with definite Hp infection (positive result in any one of the 13C/14C urea breath test, rapid urease test, and fecal Hp antigen test) who have never received Helicobacter pylori eradication treatment;
For women of child - bearing age, it is required to use medically acceptable contraceptive methods during the trial period and within 30 days after the end of the trial.
Disqualifiers
Patients who have been definitely diagnosed with Hp infection and have received antibiotic eradication treatment;
Patients with contraindications to the study drug or who are allergic to the study drug;
Patients with severe organ damage and complications (such as liver cirrhosis, uremia, etc.), severe or unstable cardiopulmonary or endocrine diseases;
Patients who have been continuously using anti - ulcer drugs (including taking PPI within 2 weeks before the Hp infection test), antibiotics or bismuth complexes (more than 3 times a week within 1 month before screening);
Trial design
Treatments tested in this trial
- Vonoprazan
- Tetracycline 500mg tid
- Minocycline
- Bismuth
- Clarithromycin 500 mg
- Amoxicillin
Treatment groups
Sponsors and collaborators
Yongquan Shi
Lead sponsor
Xijing Hospital of Digestive Diseases
Sponsor institution