Levofloxacin-Based Sequential Therapy Versus Bismuth Quadruple Therapy for Helicobacter Pylori Eradication

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorUniversity of Health Sciences Lahore

About this trial

This randomized controlled trial aims to compare the efficacy and safety of levofloxacin-based sequential therapy versus bismuth-based quadruple therapy for eradication of Helicobacter pylori infection in adult patients. Helicobacter pylori infection remains highly prevalent in developing countries and is associated with gastritis, peptic ulcer disease, mucosa-associated lymphoid tissue lymphoma, and gastric cancer. Increasing antibiotic resistance has reduced the effectiveness of conventional treatment regimens, creating a need for alternative first-line therapies with improved eradication rates and acceptable tolerability.

Eligible adult patients diagnosed with H. pylori infection by stool antigen testing will be recruited from the Gastroenterology Department of Services Hospital Lahore. Participants will be randomly assigned in a 1:1 ratio to receive either levofloxacin-based sequential therapy or bismuth-based quadruple therapy for 14 days.

The primary outcome of the study is successful eradication of H. pylori infection, confirmed by stool antigen testing performed 6 weeks after completion of therapy. Secondary outcomes include treatment-related adverse effects, treatment compliance, and overall treatment cost.

The study aims to identify an effective and affordable treatment strategy for H. pylori eradication in a population with high antibiotic resistance and socioeconomic limitations.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 20 years and older

Confirmed Helicobacter pylori infection by stool antigen testing

Willingness to comply with the assigned treatment regimen

Ability to provide informed consent

Disqualifiers

Use of antibiotics within 4 weeks prior to enrollment

Active gastrointestinal infection other than Helicobacter pylori

Previous gastrointestinal tract surgery

Pregnant or lactating females

Trial design

Design model

Parallel

Treatments tested in this trial

  • Levofloxacin-Based Sequential Therapy

    Other intervention

    Participants will receive a 14-day levofloxacin-based sequential therapy regimen. During days 1-7, participants will receive dexlansoprazole 60 mg twice daily and amoxicillin 1 g twice daily. During days 8-14, participants will receive dexlansoprazole 60 mg twice daily, levofloxacin 500 mg once daily, and tinidazole 500 mg twice daily.

  • Bismuth-Based Quadruple Therapy

    Other intervention

    Participants will receive a 14-day bismuth-based quadruple therapy regimen consisting of bismuth subsalicylate 265 mg (two tablets) twice daily, dexlansoprazole 60 mg twice daily, doxycycline 100 mg twice daily, and tinidazole 500 mg twice daily.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Levofloxacin-Based Sequential TherapyExperimental treatment 1 intervention
Group B: Bismuth-Based Quadruple TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Helicobacter pylori Eradication Rate

Time frame
6 weeks after completion of therapy

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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