Trials / Completed
CompletedNCT02873065
Efficacy and Safety of 1-week Triple Therapy With Ilaprazole for the Eradication of Helicobacter Pylori
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- —
- Sponsor
- Livzon Pharmaceutical Group Inc. · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
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
Detailed description
Participants are defined as persons who have endoscopically confirmed on gastric or duodenal ulcer(including scar stage) ,gastritis and dyspepsia confirmed to be H.pylori positive patients in the biopsy and UBT test. For 7 days, Participants treated as Esoprazole based triple regimen therapy therapy including Esoprazole 20mg,Clarithromycin 500mg and Amoxicillin Cap(Amoxicillin) 1000mg BID. After treatment, The healing rate was evaluated in the UBT test and Biopsy at 49±5days from the first day dosing
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ilaprazole | |
| DRUG | Esoprazole |
Timeline
- Start date
- 2014-09-01
- Primary completion
- 2015-06-01
- Completion
- 2015-06-01
- First posted
- 2016-08-19
- Last updated
- 2016-08-19
Source: ClinicalTrials.gov record NCT02873065. Inclusion in this directory is not an endorsement.