This study compared efficacy and safety of Ilaprazole based triple regimen therapy including
Ilaprazole 5mg, Clarithromycin 500mg and Amoxicillin Cap(Amoxicillin) 1000mg BID on the first
line eradication treatment of H.pylori
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT02873065
Ages eligible for Study
18 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
Subject must have endoscopically confirmed on gastric, duodenal ulcer(including scar) or gastritis confirmed to be H.pylori positive patients in the biopsy and UBT test.
Subject who fully understands conditions of clinical trial.
Subject who agrees to participate and spontaneously sign the ICF
Known hypersensitivity to any component of ilaprazole, Esoprazole, Amoxicillin and Clarithromycin
Subjects who are taking contraindicated medications for experimental and concomitant drug
Administrated of PPI, antibiotic medication within 4 weeks prior to commencement of the study
Pregnant and/or lactating women
Reproductive aged women not using contraception
Uncontrolled liver dysfunction
Subjects with a history of digestive malignancy within 5 years
Subjects with a history of gastrectomy or esophagectomy
Subjects with hereditary diseases such as Galactose intolerance, Lapp lactose deficiency, glucose-galactose malabsorption
Subjects participating in a clinical trial before another trial within 30 days
Inconsistent judged subject by researcher
All locations for NCT02873065
View full eligibility
Tris trial is registered with FDA with number: NCT02873065. The sponsor of the trial is Livzon Pharmaceutical Group Inc. and it is looking for 0 volunteers for the current phase.
Official trial title:
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