Clinical Trials Directory

Trials / Completed

CompletedNCT03716622

A Comparison of Clarithromycin-based and Furazolidone-based Bismuth-containing Regimens for H. Pylori Eradication

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
350 (actual)
Sponsor
Shandong University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

We aim to assess and compare the effectiveness of clarithromycin- and furazolidone-based regimens as primary therapies in eradicating H. pylori.

Detailed description

Helicobacter pylori plays a pivotal role in many diseases such as peptic ulcer disease and MALT lymphomas. And the prevalence of H. pylori is increasing in some parts of the world. However, the eradication becomes increasingly difficult due to the growing antibiotic resistance. Bismuth-containing quadruple regimens are now recommended to serve as first-line therapies. Bismuth-clarithromycin-containing and bismuth-furazolidone-containing quadruple regimens are both in the list of the first regimens. And recent antimicrobial susceptibility tests showed us that the clarithromycin was increasingly resisted while furazolidone remained hardly resisted. The comparison between the effects of bismuth-clarithromycin-containing and bismuth-furazolidone-containing quadruple regimens is not so clear.

Conditions

Interventions

TypeNameDescription
DRUGFurazolidonebismuth-furazolidone-containing quadruple regimens
DRUGClarithromycinbismuth-clarithromycin-containing quadruple regimens

Timeline

Start date
2018-07-31
Primary completion
2019-08-31
Completion
2019-08-31
First posted
2018-10-23
Last updated
2020-06-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03716622. Inclusion in this directory is not an endorsement.