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Vonoprazan-Minocycline Dual Therapy as a First-Line Treatment of Helicobacter pylori Infection Compared With Empirical Bismuth-Containing Quadruple Therapy

Vonoprazan-Minocycline Dual Therapy as a First-Line Treatment of Helicobacter pylori Infection Compared With Empirical Bismuth-Containing Quadruple Therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081461
Enrollment
Unknown
Registered
2024-03-01
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Helicobacter pylori Infection

Interventions

Experimental group:Vonoprazan 20mg twice a day + Minocycline 100mg twice a day
control group:Rabeprazole 10mg twice/day + bismuth potassium citrate 220mg twice/day + amoxicillin 1000mg twice/day + clarithromycin 500mg twice/day

Sponsors

Department of Gastroenterology, Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-70 years old, male or female; (2) 13C urea breath test indicates Helicobacter pylori positive infection, and the doctor determines that the eradication of H.pylori treatment is necessary; (3) Meet the indication of Helicobacter pylori eradication (according to the Sixth National Consensus Report on Helicobacter pylori Infection Treatment); (4) Infected persons who have not previously received eradication therapy for Helicobacter pylori infection

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women; (2) Allergic to the therapeutic drugs used in the eradication programme; (3) Patients who are taking azanavir sulfate, Ripiavirin, or terphenadine; (4) Previous history of gastric or esophageal surgery; (5) Patients with severe cardiovascular and cerebrovascular diseases (including arrhythmia, bradycardia, prolonged Q-T interval, ischemic heart disease, congestive heart failure, etc.), liver and kidney insufficiency, and abnormal coagulation function; (6) uncontrolled acute disease; (7) Previous history of digestive system tumors; (8) Taking drugs such as PPI and H2 blockers that may affect the study results within 1 month.

Design outcomes

Primary

MeasureTime frame
Eradication rate;Adverse effects rate, ADR;

Secondary

MeasureTime frame
compliance;

Countries

China

Contacts

Public ContactWeihong Wang

Department of Gastroenterology, Peking University First Hospital

wangweihong2581@163.com+86 130 4117 1610

Outcome results

None listed

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