Clinical Trials Directory

Trials / Completed

CompletedNCT02547038

Comparing the Efficacy of Reverse Hybrid Therapy and Bismuth Quadruple Therapy

Comparing the Efficacy and Impact on Gastrointestinal Microbiome of Reverse Hybrid Therapy and Bismuth Quadruple Therapy in Helicobacter Pylori Eradication

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
352 (actual)
Sponsor
Kaohsiung Veterans General Hospital. · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Reverse hybrid therapy achieves a higher eradication rate than bismuth quadruple therapy remained unanswered.

Detailed description

A 14-day hybrid therapy invented by our study group appears very promising in H. pylori eradication, achieving excellent eradication rates of 99% and 97% according to per-protocol and intention-to-treat analyses, respectively. Recently, the investigators demonstrated that the eradication rate of reverse hybrid therapy was higher than that of standard triple therapy. However, whether reverse hybrid therapy achieves a higher eradication rate than bismuth quadruple therapy remained unanswered.

Conditions

Interventions

TypeNameDescription
DRUGpantoprazole+bismuth+tetra+metropantoprazole 40 mg twice daily, bismuth subcitrate 120 mg four times daily, and tetracycline 500 mg four times daily, and metronidazole 250 mg four times daily for 14 days
DRUG(panto+amox+clar+metr)+(panto+amox)a 7-day quadruple regimen with pantoprazole 40 mg twice daily, amoxicillin 1 g twice daily, clarithromycin 500 mg twice daily, and metronidazole 500 mg twice daily, followed by a 7-day dual regimen with pantoprazole 40 mg twice daily and amoxicillin 1 g twice daily

Timeline

Start date
2015-02-01
Primary completion
2018-10-01
Completion
2018-10-01
First posted
2015-09-11
Last updated
2019-06-10
Results posted
2019-06-10

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02547038. Inclusion in this directory is not an endorsement.