Clinical Trials Directory

Trials / Completed

CompletedNCT01667575

Efficiency Study of Clarithromycin and Bismuth-containing Quadruple Therapy to Treat H.Pylori

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
180 (actual)
Sponsor
Shanghai Jiao Tong University School of Medicine · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to observe the efficacy of ten day triple therapy-based, bismuth-containing quadruple therapy for H.pylori treatment.

Detailed description

The success rate of currently recommended triple therapy with a proton pump inhibitor (PPI) plus amoxicillin and clarithromycin has fallen into the unacceptable range. The purpose of this study is to observe the efficacy of ten day triple therapy-based, bismuth-containing quadruple therapy for H.pylori treatment, while ten day triple therapy is used as control.

Conditions

Interventions

TypeNameDescription
DRUGEsomeprazoleantisecretary drug of the quadruple therapy
DRUGAmoxicillinantibiotic of the quadruple therapy
DRUGClarithromycinantibiotic of the quadruple therapy
DRUGBismuth Potassium Citrateone of a component of a quadruple therapy
OTHERlong duration (14 day)

Timeline

Start date
2012-08-01
Primary completion
2013-05-01
Completion
2013-05-01
First posted
2012-08-17
Last updated
2013-06-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01667575. Inclusion in this directory is not an endorsement.