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UnknownNCT01922765

Concomitant Therapy of H. Pylori

Evaluation of the Efficacy of Concomitant Therapy for Eradication of Helicobacter Pylori

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
540 (estimated)
Sponsor
The Catholic University of Korea · Academic / Other
Sex
All
Age
19 Years – 75 Years
Healthy volunteers
Not accepted

Summary

If we compare eradication rate of Helicobacter pylori divided to 4 groups: amoxicillin, rabeprazole, clarithromycin(AOC), amoxicillin, rabeprazole, metronidazole(AOM), treated with amoxicillin, rabeprazole for 5 day, followed by clarithromycin, metronidazole, rabeprazole for 5 days(sequential), amoxicillin, clarithromycin, metronidazole, rabeprazole(concomitant), then the eradication rate of concomitant group will be the highest.

Detailed description

* Subject: The patient of gastritis, gastric ulcer, and duodenal ulcer infected with Helicobacter pylori * 170 subjects per group * Eradication regimens are as follows: AOC group, treated with amoxicillin, rabeprazole, clarithromycin for 7 days; AOM group, treated with amoxicillin, rabeprazole, metronidazole for 7 days; sequential group, treated with amoxicillin, rabeprazole for 5 day, followed by clarithromycin, metronidazole, rabeprazole for 5 days; concomitant group, treated with amoxicillin, clarithromycin, metronidazole, rabeprazole for 7 days

Conditions

Interventions

TypeNameDescription
DRUGamoxicillin, clarithromycin, metronidazole, rabeprazole

Timeline

Start date
2013-08-01
Primary completion
2014-02-01
Completion
2014-02-01
First posted
2013-08-14
Last updated
2014-02-11

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01922765. Inclusion in this directory is not an endorsement.

Concomitant Therapy of H. Pylori (NCT01922765) · Clinical Trials Directory