Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | amoxicillin, 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.