Randomized Study on Efficacy of Gemifloxacin-based Regimen for Helicobacter Pylori Infection
Helicobacter Pylori Infection
About this trial
This is an interventional treatment trial for Helicobacter Pylori Infection
Eligibility Criteria
Inclusion Criteria:
- Patients aged 19-70 years with H. pylori infection
The presence of H. pylori was defined as positive if the results of one of the following two tests were positive:
- Rapid urease test (CLO™, Delta West, Bentley, Western Austria)
- Histology. Biopsy specimens, obtained by endoscopy, were fixed in formalin and used for determination of H. pylori infection by Giemsa staining.
Exclusion Criteria:
- Patients with previous H. pylori eradication therapy
- Patients treated with H2 receptor antagonist, PPI, and antibiotics in the previous 4 weeks, or nonsteroidal anti-inflammatory drug (NSAID) in the previous 2 weeks
- Pregnant or lactating women
- Patients who suffered from serious diseases such as severe liver disease, renal disease, and cerebrovascular disease
- Patients who had a drug allergy to the study drugs
- Patients with previous gastric surgery.
Sites / Locations
- Samsung Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Standard triple therapy
Gemifloxacin-based triple therapy
Rabeprazole (Rabiet®, ildong pharmaceutical Co. Ltd., Seoul, Korea) 20 mg twice daily, amoxicillin (Pamoxin®, Dongwha Co. Ltd., Seoul, Korea) 1 g twice daily, and clarithromycin (Klaricid®, Abbot Korea Co. Ltd., Seoul, Korea) 500 mg twice daily for 7 days
Rabeprazole (Rabiet®, ildong pharmaceutical Co. Ltd., Seoul, Korea) 20 mg twice daily, amoxicillin (Pamoxin®, Dongwha Co. Ltd., Seoul, Korea) 1 g twice daily, and gemifloxacin (Factive®, LG Life Sciences, Ltd, Seoul, Korea) 320 mg once daily for 7 days