Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06065267

Levofloxacin Concomitant Versus Levofloxacin Sequential

Efficacy of Two-week Therapy With Levofloxacin-based Concomitant Regimen Versus Levofloxacin-based Sequential Regimen for Helicobacter Pylori Infection in Syrian Population: a Prospective Single-center Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Damascus Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The goal of this trial is to determine the efficacy of levofloxacin based sequential treatment regimen or concomitant levofloxacin based regimens as empirical first-line therapy in the Syrian population

Conditions

Interventions

TypeNameDescription
DRUGsequentialamoxicillin 1000 mg bid ,esomprazole 20 bid for one week then levofloxacine 500 mg q.d, metraonidazoel 500 500 bid, and esomprazole 20 bid for one week
DRUGLevofloxacin 500Mg Oral TabletLevofloxacin 500 mg qd, amoxicillin 500 2cab bid,Tinadizole 500 bid, esomprazole 20 bid

Timeline

Start date
2024-01-02
Primary completion
2026-12-31
Completion
2027-06-30
First posted
2023-10-03
Last updated
2023-10-03

Locations

1 site across 1 country: Syria

Source: ClinicalTrials.gov record NCT06065267. Inclusion in this directory is not an endorsement.