Efficacy and Safety of Dual Therapy for Helicobacter Pylori Eradication

This study intends to select the patients with Hp infection in 11 tertiary hospitals across our country, and randomly give the two therapies to compare the eradication rate, compliance, the rate of adverse events, so as to provide some advices for the selection of appropriate eradication therapy, then collect an efficient, convenient and safe therapy for patients with H.pylori infection.

Before receiving the treatment plan, general information and relevant medical history of the subjects were collected through electronic questionnaires.The experimental data will be collected and recorded through follow-up by phone or WeChat during the experiment.

Inclusion criteria

• Ages between 18 and 65 years; Sexes eligible for study: both;
• patients who are diagnosed with Helicobacter pylori;
• treatment-naive patients or patients who failed to eradicate Helicobacter pylori in the past but haven't undergone eradication therapy in the past six months;
• voluntary to be involved in the study and written informed consent was obtained from all patients

Exclusion criteria

• allergic reactions to the study drugs;
• patients with peptic ulcer;
• patients who underwent eradication therapy for Helicobacter pylori during the last six months;
• patients who took antibiotics,bismuth agents,probiotics within four weeks prior to treatment and those who took H2 receptor antagonists,proton pump inhibitors(PPIs) or potassium competitive acid blockers within two weeks prior to treatment;
• patients who are taking glucocorticoids, non-steroidal anti-inflammatory drugs or anticoagulants;
• patients who have history of esophageal or gastric surgery;
• pregnant or lactating women;
• patients who have severe concurrent diseases such as hepatic,cardiovascular,respiratory,renal disorders or malignancies;
• Alcohol abusers