Clinical Trials Directory

Trials / Completed

CompletedNCT05863858

Eradication of H. Pylori Infection With Moxifloxacin

High Eradication Rate of Helicobacter Pylori Infection With Moxifloxacin-Based Triple Therapy in Comparison With Levofloxacin-Based Sequential Therapy: Randomized Controlled Trials

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
162 (actual)
Sponsor
Iyad Naeem Muhammad, PhD · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The main objective of the study is to compare the effectiveness of moxifloxacin triple therapy with levofloxacin-based sequential therapy in terms of eradication rate, safety, and patient compliance.

Detailed description

Patients who were confirmed to be positive for Helicobacter Pylori infection were randomly assigned to the eradication treatments. At four weeks after completion of eradication therapy, H. pylori tests were performed with a Stool antigen test.

Conditions

Interventions

TypeNameDescription
DRUGSequential Regimen: Levofloxacin 500 mg BID, Amoxicillin 1 gm BID, omeprazole 20 mg BID for first five days followed by Levofloxacin 500 mgBID, Tinidazole 500 mg BID, Omeprazole 20 mg BIDThe eradication rate of H. Pylori with levofloxacin-based sequential therapy
DRUGTriple Regimen: Moxifloxacin 400mg OD, Amoxicillin 1 gm BID, Omeprazole 20mgBIDThe eradication rate of H. Pylori with moxifloxacin-based triple therapy

Timeline

Start date
2020-06-01
Primary completion
2021-12-01
Completion
2022-06-08
First posted
2023-05-18
Last updated
2023-05-18

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT05863858. Inclusion in this directory is not an endorsement.