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
| Type | Name | Description |
|---|---|---|
| DRUG | Sequential 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 BID | The eradication rate of H. Pylori with levofloxacin-based sequential therapy |
| DRUG | Triple Regimen: Moxifloxacin 400mg OD, Amoxicillin 1 gm BID, Omeprazole 20mgBID | The 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.