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Analysis of efficacy of vonoprazan and rabeprazole in Helicobacter pylori eradication therapy

Analysis of efficacy of vonoprazan and rabeprazole in Helicobacter pylori eradication therapy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052576
Enrollment
Unknown
Registered
2021-10-31
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-10-24

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

Conditions

Helicobacter pylori infection

Interventions

7-day vonoprazan group:vonoprazan 20mg,2 times a day for 7days
14-day vonoprazan group:vonoprazan 20mg,2 times a day for 14 days
14-day rabeprazole group:rabeprazole 10mg,2 times a day for 14 days

Sponsors

Department of Gastroenterology, Jinshan Hospital of the First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 20 to 70 years; 2. Gastroscopy showed chronic gastritis; 3. After 13C breath test or biopsy of gastric mucosa under gastroscope, Helicobacter pylori infection was found; 4. Sign informed consent; 5. Did not participate in other research projects in recent three months.

Exclusion criteria

Exclusion criteria: 1. History of receiving H.pylori eradication therapy; 2. Those who had received antibiotics, bismuth and PPI within 4 weeks; 3. Acute upper gastrointestinal bleeding, acute gastric mucosal lesions, gastroesophageal reflux, peptic ulcer, gastrinoma, Zollinger-Ellison syndrome, patients who have undergone surgery (upper gastrointestinal resection or vagotomy) that may affect gastric acid secretion, or other patients with gastric acid secretion disorder; 4. Accompanied by serious or unstable heart, liver, kidney, endocrine, blood and other physical diseases or malignant tumors; 5. Those who allergy to any of the study drugs; 6. Those who had used drugs that had an impact on the efficacy evaluation before treatment; 7. Lactation, pregnancy or planned pregnancy during the trial period; 8. Patients with severe cognitive impairment and not cooperating with treatment.

Design outcomes

Primary

MeasureTime frame
Eradication rates of H. pylori;

Countries

China

Contacts

Public ContactGu Sai

Jinshan Hospital, the First Affiliated Hospital of Chongqing Medical University

1601792466@qq.com+86 13018339696

Outcome results

None listed

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