Clinical Trials Directory

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

TypeNameDescription
DRUGBismuthBismuth 220mg b.i.d for 2 weeks
DRUGLansoprazoleLansoprazole 30 mg b.i.d.for 2 weeks
DRUGLevofloxacinLevofloxacin 0.5 q.d. for 2 weeks
DRUGAmoxicillinAmoxicillin 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.

Bismuth Improves the Efficacy of Levofloxacin-containing Triple Therapy for Helicobacter Pylori Treatment (NCT01667718) · Clinical Trials Directory