Simplified Dual Regimen Guided by Fecal Clarithromycin Resistance Gene Detection for First-line H. Pylori Eradication

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorPeking University First Hospital

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

Treatment groups

70 Participants
are divided into 1 treatment group