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Clinical Trials in Egypt / NCT07293910
Recruiting Phase 2

Vonoprazan vs Proton Pump Inhibitor With Vitamin D or Probiotics Based Triple Therapy for Eradication of Helicobacter Pylori Infection

NCT07293910 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 2
Started
2026-02-15
Last updated
2026-09-09

Condition(s) studied

HELICOBACTER PYLORI INFECTIONSHelicobacter InfectionHelicobacter Pylori Gastrointestinal Tract InfectionHelicobacter Pylori Infected Patients

Investigational drug(s) / intervention(s)

VonoparazanVitamin D →ProbioticAmoxicillin →Clarithromycin 500 mg →Proton Pump Inhibitor (PPI) Therapy

Vonoparazan: Vonoprazan: Potassium competitive acid blocker

Vitamin D: MIcronutrient

Probiotic: Lactobacillus acidophilus

Amoxicillin: Amoxicillin is penicillin-type antibiotic used to treat a wide range of bacterial infections.

Clarithromycin 500 mg: Clarithromycin is a prescription macrolide antibiotic used to treat a variety of bacterial infections

Proton Pump Inhibitor (PPI) Therapy: Proton Pump Inhibitors (PPIs) are powerful medications that significantly reduce stomach acid production by blocking the H+/K+ ATPase enzymes (proton pumps) in the stomach lining,

Study summary

Helicobacter pylori is a Gram-negative, spiral-shaped bacterium that infects up to 50% of the world's population, residing in the gastric mucosa and using the mucus layer for protection from the stomach's high acidity. Its clinical significance is profound: it is classified as a Group 1 carcinogen by the World Health Organization and is a primary cause of chronic gastritis, peptic ulcers, gastric lymphoma, and gastric carcinoma. The current first-line treatment, a PPI-based triple therapy (PPI + clarithromycin + amoxicillin), is experiencing a decline in efficacy (cure rates of 50-70%) due to widespread antibiotic resistance and compliance issues. To overcome this, newer agents like Vonoprazan Fumarate, a Potassium-Competitive Acid Blocker (P-CAB), are being adopted. Vonoprazan works by reversibly inhibiting the H+, K+ ATPase pump achieving stronger and longer-lasting acid suppression than PPIs because it does not require acid activation and is more stable in an acidic environment. In addition to pharmacological treatment, adjunctive therapies show promise. Vitamin D, acting through Vitamin D Receptor (VDR), assists in eradication by upregulating antimicrobial proteins like beta-defensin and cathelicidin, and its metabolite can cause bacterial cell lysis. Probiotics (primarily Lactobacillus and Bifidobacterium strains) enhance eradication rates by restricting bacterial growth, inhibiting adhesion, and exerting an anti-inflammatory effect through decreased interleukin-8 production. Finally, helicobacter pylori infection is marked by significant inflammation and oxidative stress. The bacterial protein TIP alpha induces high levels of the pro-inflammatory cytokine TNF alpha. Furthermore, the infection increases free radical production, leading to oxidative stress reflected by high levels of malondialdehyde. Systemic inflammation is also evident as helicobacter pylori infection is associated with significantly elevated serum C-reactive protein levels, which decrease upon successful eradication.

Aim of the work:

This study aims at evaluating the safety and efficacy of Vonoprazan vs Proton Pump Inhibitor with Vitamin D or Probiotics Based Triple Therapy for Eradication of Helicobacter Pylori Infection.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Both male and female patients. • Patients ≥ 18 and \<80 years old. Patients with confirmed diagnosis of H. pylori infection using either stool antigen test, urea breath test or endoscopy (n=66) Patient whom are confirmed to be H-pylori negative using either stool antigen test, urea breath test or endoscopy (n=66) Exclusion Criteria: * Pregnant or lactating patients. • Patients with inflammatory diseases. • Patients sensitive to any of the regimens' components. • Patients who had received a previous eradication therapy, recent use of antimicrobial agents, proton pump inhibitors, and H2 receptor blockers within 1 month. Patients with previous incidents of gastric or duodenal bleeding, gastric surgery or gastric malignancy. • Patients with active liver disease. • Patients with renal impairment. • Concurrent use of liver enzyme inducers, inhibitors or drugs with high plasma protein binding.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National liver institute - Menoufia university - egypt Shibīn al Kawm Egypt Recruiting

On this site

📄 Amoxil (amoxicillin) drug profile →

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07293910 on ClinicalTrials.gov ↗ ← All trials in Egypt