Clinical Trials Directory

Trials / Completed

CompletedNCT02646332

Comparing the Efficacy of Reverse Hybrid Therapy and Concomitant Therapy

Comparing the Efficacy and Impact on Gastrointestinal Microbiota of Reverse Hybrid Therapy and Concomitant Therapy in Helicobacter Pylori Eradication

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
248 (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 concomitant therapy remains 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 concomitant therapy remains unanswered.

Conditions

Interventions

TypeNameDescription
DRUG(dexlan+amox+clar+metr)+(dexlan+amox)a 7-day quadruple regimen with dexlansoprazole MR 60 mg once 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 dexlansoprazole MR 60 mg once daily and amoxicillin 1 g twice daily
DRUGdexlan+clarith+amox+metrodexlansoprazole MR 60 mg once daily, amoxicillin 1 g twice daily, clarithromycin 500 mg twice daily, and metronidazole 500 mg twice daily for 14 days

Timeline

Start date
2015-12-01
Primary completion
2020-07-31
Completion
2020-08-31
First posted
2016-01-05
Last updated
2020-11-24
Results posted
2020-11-24

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02646332. Inclusion in this directory is not an endorsement.