Efficacy of Different Durations of Dual and Quadruple Regimens for Helicobacter Pylori Eradication

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-70
SponsorShandong University

About this trial

The study aimed to compare the efficacy and safety of dual and quadruple regimens with different durations (7-day, 10-day, 14-day) for the eradication of Helicobacter pylori. Subjects were randomized to receive the intervention and were reviewed by 13C-urea breath test after 6 weeks. The eradication rates, adverse reaction rates and patient adherence were calculated.

Eligibility criteria

Qualifiers

Patients aged 18-70 years old

Patients with H.pylori infection (13C/14C-urea breath test)

Patients without previous treatment for H. pylori eradication

Disqualifiers

Patients with serious underlying diseases, such as liver insufficiency (Aspartate aminotransferase or alanine aminotransferase greater than the normal value), renal insufficiency (Cr≥2.0mg/dL or glomerular filtration rate <50 ml/min), immunosuppression, malignant tumors, Coronary heart disease or coronary artery stenosis ≥75%

Patients with active gastrointestinal bleeding

Patients with a history of upper gastrointestinal surgery

Patients allergic to treatment drugs

Trial design

Treatments tested in this trial

  • vonoprazan+amoxicillin
  • Duration of eradication regimen: 7-day
  • vonoprazan+amoxicillin+tetracycline+bismuth
  • Duration of eradication regimen: 10-day
  • Duration of eradication regimen: 14-day

Treatment groups

330 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Shandong University

Lead sponsor

Zibo Maternal and Child Health Hospital

Collaborator

Zaozhuang Municipal Hospital

Collaborator

Feicheng Municipal People's Hospital

Collaborator

Shandong University of Traditional Chinese Medicine

Collaborator

The People's Hospital of Jimo.Qingdao

Collaborator

Dezhou Hospital Qilu Hospital of Shandong University

Collaborator