Comparison of Two Dual Therapies in the First-line Treatment of Helicobacter Pylori Infection (SHARE2301)
Helicobacter Pylori Infection
About this trial
This is an interventional treatment trial for Helicobacter Pylori Infection
Eligibility Criteria
Inclusion Criteria: Helicobacter pylori infection (either positive for histopathological test, rapid urease test, or C13/C14 urea breath test). Patients who have not previously received helicobacter pylori eradication therapy. Exclusion Criteria: Serious underlying diseases, such as liver insufficiency, renal insufficiency, immunosuppression, malignant tumor, coronary heart disease (angina pectoris or coronary artery stenosis ≥ 75%). Those who are not willing to take contraceptive measures during pregnancy, lactation or the trial. Active gastrointestinal bleeding. History of drug allergy. History of upper gastrointestinal surgery. Medication history of bismuth, antibiotics and PPI within 4 weeks. Other behaviors that may increase the risk, such as alcohol and drug abuse. Unable or unwilling to provide informed consent.
Sites / Locations
- Department of Gastroenterology, Qilu Hospital, Shandong UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
14-day Tegoprazan-Amoxicillin dual therapy
14-day Esomeprazole-Amoxicillin dual therapy
14-day Tegoprazan-Amoxicillin dual therapy, Tegoprazan(Luo Xin Pharmaceutical Group Co. LTD)50mg bid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid
14-day Esomeprazole-Amoxicillin dual therapy, Esomeprazole(Astrazeneca Pharmaceutical Co., LTD.) 20mg qid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid