Skip to content

Comparison of Levofloxacin based therapy and Hybrid therapy for the treatment of Helicobacter pylori infection

Levofloxacin based therapy vs Hybrid therapy in the eradication of Helicobacter pylori: A randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047108
Enrollment
122
Registered
2022-11-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K279- Peptic ulcer, site unspecified, unspecified as acute or chronic, without hemorrhage or perforation

Interventions

Intervention1: Regimen for H.pylori: Levofloxacin based therapy. Tab amoxicillin 1 g twice a day Tab levofloxacin 500 mg twice a day Cap omeprazole 20 mg twice a day - all for 14 days in 1 arm cons

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: adult patients of age 18-80 years with peptic ulcer disease will be included

Exclusion criteria

Exclusion criteria: 1.Previous eradication therapy. 2.Patients who have used antibiotics within the previous 4 weeks. 3.Past history of developing allergy to any antibiotic used in the study. 4.Patients who have undergone gastrectomy. 5.Coexisting of severe concomitant illness. 6. Pregnancy or lactating women. 7.Patients diagnosed with any malignancies. Patients with portal gastropathy.

Design outcomes

Primary

MeasureTime frame
To compare efficacy of H. pylori eradication between levofloxacin-based therapy and hybrid therapy in patients with upper gastrointestinal disease needing eradicationTimepoint: 6 weeks The assessment of eradication which determines the efficacy will be at 6 weeks following the completion of therapy

Secondary

MeasureTime frame
To compare the compliance and adverse effects of levofloxacin-based therapy and hybrid therapy.Timepoint: Compliance will be measured at the end of therapy (2weeks). Adverse effects will be measured during and 1 week after the therapy (1-3 weeks of commencement of therapy )

Countries

India

Contacts

Public ContactDr Rajalekshmy M R

JIPMER

drvikramkate@gmail.com9843058013

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026