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A single-center randomized controlled study of Vonoprazan based dual therapy and Rabeprazole based dual therapy for Helicobacter pylori infection.

A single-center randomized controlled study of Vonoprazan based dual therapy and Rabeprazole based dual therapy for Helicobacter pylori infection.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077528
Enrollment
Unknown
Registered
2023-11-11
Start date
2023-11-20
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

Helicobacter

Interventions

B:Rabeprazole+Amoxicillin
A:Vonoprazan + Amoxicillin

Sponsors

Nanjing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: Age 18-70 years old 2: Patients diagnosed with Helicobacter pylori positivity through 13C-UBT or 14C-UBT 3: Patients who have not received eradication treatment for Helicobacter pylori in the past, or who have failed eradication in the early stage but have not received eradication treatment within six months 4: Voluntarily participate in this experiment and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1: Allergies to research drugs (such as those allergic to penicillin) 2: Patients with chronic gastritis accompanied by peptic ulcer 3: Patients who have received Helicobacter pylori eradication treatment within six months 4: Use antibiotics or bismuth medication 4 weeks before starting the study 5: use P-CAB or PPI 2 weeks before starting the study 6: Using corticosteroids, non steroidal anti-inflammatory drugs, or anticoagulants 7: History of esophageal or gastric surgery 8: Pregnant or lactating women 9: Suffering from serious concomitant diseases such as liver disease, cardiovascular disease, lung disease, or kidney disease 10: Excessive drinking; 11. Gastric mucosal associated lymphoid tissue lymphoma (MALT), malignant tumor disease.

Design outcomes

Primary

MeasureTime frame
eradication rate;Patient compliance;

Secondary

MeasureTime frame
Incidence of adverse reactions;

Countries

China

Contacts

Public ContactZhang Zhenyu

Nanjing First Hospital

zzy6565@sina.com+86 189 5167 0222

Outcome results

None listed

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