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
| Type | Name | Description |
|---|---|---|
| DRUG | sequential | amoxicillin 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 |
| DRUG | Levofloxacin 500Mg Oral Tablet | Levofloxacin 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.