Trials / Completed
CompletedNCT01667718
Bismuth Improves the Efficacy of Levofloxacin-containing Triple Therapy for Helicobacter Pylori Treatment
Levofloxacin-containing Therapy for Helicobacter Pylori Treatment
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 161 (actual)
- Sponsor
- Shanghai Jiao Tong University School of Medicine · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
To examine and compare the efficacy of 2 week Levofloxacin-containing therapies with and without Bismuth for H.pylori treatment.
Detailed description
The success rate of the standard triple therapy for H. pylori infection is decreasing recently.Fluoroquinolone has been proposed to replace clarithromycin as an alternative in the treatment. However prevalence of H.pylori resistance to Levofloxacin has increased rapidly in our area. The purpose of this study is to observe the efficacy of 14 day Levofloxacin triple therapy-based, bismuth-containing quadruple therapy for H.pylori treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bismuth | Bismuth 220mg b.i.d for 2 weeks |
| DRUG | Lansoprazole | Lansoprazole 30 mg b.i.d.for 2 weeks |
| DRUG | Levofloxacin | Levofloxacin 0.5 q.d. for 2 weeks |
| DRUG | Amoxicillin | Amoxicillin 1 g b.i.d. for 2 weeks |
Timeline
- Start date
- 2012-05-01
- Primary completion
- 2012-10-01
- Completion
- 2012-10-01
- First posted
- 2012-08-17
- Last updated
- 2012-12-13
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT01667718. Inclusion in this directory is not an endorsement.