About this trial
To investigate the efficacy, safety, and compliance of a simplified strategy using vonoprazan plus clarithromycin for first-line treatment in patients with Helicobacter pylori infection, among those infected with strains without clarithromycin resistance gene mutations based on fecal clarithromycin resistance gene detection.
Eligibility criteria
Qualifiers
Aged 18-70 years;
Positive results for both ¹³C-urea breath test (¹³C-UBT) and fecal polymerase chain reaction (PCR), confirming Helicobacter pylori infection, with a clinical indication for H. pylori eradication as judged by the physician;
Treatment-naïve individuals with no prior history of H. pylori eradication therapy.
Disqualifiers
Pregnant or lactating women
Patients with a history of allergy to any drugs used in the eradication regimen
Patients with severe systemic diseases or malignant tumors
History of gastric resection surgery
Trial design
Treatments tested in this trial
- Vonoprazan 20 mg twice daily + clarithromycin 500 mg twice daily for 14 days