Clinical Trials Directory

Trials / Completed

CompletedNCT02547025

Personalized Treatment for Refractory H Pylori Infection

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

Summary

In this study, the investigators develop a personalized treatment according to culture-guided antibiotics plus high-dose proton-pump inhibitor and bismuth to treat refractory H pylori infection.

Detailed description

They are categorized into three groups: (1) patients who have positive result of culture with equal to or more than three susceptible antibiotics are treated by non-bismuth quadruple therapy (rabeprazole 20 mg q.d.s. and three effective antibiotics), (2) patients who have positive result of culture with one or two susceptible antibiotics are treated by bismuth-containing therapy (rabeprazole 20 mg q.d.s., bismuth subcitrate 120 mg q.d.s. and all the effective antibiotics), and (3) patients who have negative result of culture or whose culture data are unavailable will be treated by (rabeprazole 20 mg q.d.s, amoxicillin 500 mg q.d.s., tetracycline 500 mg q.d.s. and levofloxacin 500 mg o.d.) for 14 days.

Conditions

Interventions

TypeNameDescription
DRUGrabeprazole+3 antibiotics(rabeprazole 20 mg q.d.s. and three effective antibiotics) for 14 days.
DRUGrabeprazole+bismuth+2 antibiotics(rabeprazole 20 mg q.d.s., bismuth subcitrate 120 mg q.d.s. and all the effective antibiotics) for 14 days.
DRUGrabeprazole+amox+tetr+levo(rabeprazole 20 mg q.d.s, amoxicillin 500 mg q.d.s., tetracycline 500 mg q.d.s. and levofloxacin 500 mg o.d.) for 14 days.

Timeline

Start date
2012-08-01
Primary completion
2021-10-31
Completion
2021-10-31
First posted
2015-09-11
Last updated
2023-10-26

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02547025. Inclusion in this directory is not an endorsement.

Personalized Treatment for Refractory H Pylori Infection (NCT02547025) · Clinical Trials Directory