Clinical Trials Directory

Trials / Completed

CompletedNCT02873065

Efficacy and Safety of 1-week Triple Therapy With Ilaprazole for the Eradication of Helicobacter Pylori

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
Sponsor
Livzon Pharmaceutical Group Inc. · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This study compared efficacy and safety of Ilaprazole based triple regimen therapy including Ilaprazole 5mg, Clarithromycin 500mg and Amoxicillin Cap(Amoxicillin) 1000mg BID on the first line eradication treatment of H.pylori

Detailed description

Participants are defined as persons who have endoscopically confirmed on gastric or duodenal ulcer(including scar stage) ,gastritis and dyspepsia confirmed to be H.pylori positive patients in the biopsy and UBT test. For 7 days, Participants treated as Esoprazole based triple regimen therapy therapy including Esoprazole 20mg,Clarithromycin 500mg and Amoxicillin Cap(Amoxicillin) 1000mg BID. After treatment, The healing rate was evaluated in the UBT test and Biopsy at 49±5days from the first day dosing

Conditions

Interventions

TypeNameDescription
DRUGIlaprazole
DRUGEsoprazole

Timeline

Start date
2014-09-01
Primary completion
2015-06-01
Completion
2015-06-01
First posted
2016-08-19
Last updated
2016-08-19

Source: ClinicalTrials.gov record NCT02873065. Inclusion in this directory is not an endorsement.

Efficacy and Safety of 1-week Triple Therapy With Ilaprazole for the Eradication of Helicobacter Pylori (NCT02873065) · Clinical Trials Directory