drugset / Trial / NCT05049902

Summary

The researchers collect treatment-naive H.pylori-positive patients from the outpatient clinic. The subjects were randomized to receive a 10-day or 14-day course of quadruple eradication therapy. 6-8 weeks after treatment, the subjects will re-take the 13C-urea breath test. Calculate the eradication rates, adverse reaction rates, patient compliance and cost-effectiveness index of each group.

Timeline

Start
2021-09-21
Primary completion
2023-05-30
Completion
2023-06-30

Outcome

Met primary endpoint

paper Compared with the 14-day bismuth-containing quadruple regimens, the 10-day regimen demonstrated a non-inferior efficacy and lower incidence of adverse effects. PMID 38700630 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Amoxicillin Other / unclassified 1000 mg —
Subject Bismuth Potassium Citrate Unknown 220 mg —
Subject Clarithromycin Small molecule 500 mg —
Subject Metronidazole Small molecule 400 mg —
Subject Tetracycline Unknown 500 mg —
Subject Vonoprazan Other / unclassified 20 mg —
Subject colloidal bismuth pectin Unknown 200 mg —