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Vonoprazan-based Bismuth Quadruple therapy containing amoxicillin and furazolidone as rescue therapy on treatment of Helicobacter pylori infection

Vonoprazan-based Bismuth Quadruple therapy containing amoxicillin and furazolidone as rescue therapy on treatment of Helicobacter pylori infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073250
Enrollment
Unknown
Registered
2023-07-05
Start date
2023-07-07
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Helicobacter pylori infection

Interventions

Sponsors

The First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Participants aged 18-70 years; 2. Patients failed in first-line eradication regimen recommended by Chinese guidelines; 3. > 6 months after the end of previous H. pylori eradication treatment; 4. Confirmed H. pylori infection by at least one of the following tests: urea breath test, histology exam and positive bacterial culture.

Exclusion criteria

Exclusion criteria: 1. Used antibiotics,bismuth,or acid inhibitor use, including H2 receptor antagonist, PPI or P-CAB within four weeks before inclusion; 2. Treated with a regimen containing amoxicillin and furazolidone for H. pylori eradication before; 3. Current pregnancy or breastfeeding; 4. Allergy to any of the study drugs; 5. History of gastrectomy; 6. Gastric malignancy; 7. Gastroduodenal ulcer with recent hemorrhage or signs of hemorrhage within 4 weeks; 8. Had severe comorbidities or physical or mental diseases; 9. Hepatic or renal dysfunction; 10. Patients with glucose-6-phosphate dehydrogenase (G-6PD) deficiency, ulcer disease or bronchial asthma; 11. Administration of azanavir, lipivirin. Tricyclic antidepressants, levodopa, acetaminophen, guaifenesin/dextromethorphan, monoamine oxidase inhibitors, or tramadol during the trial.

Design outcomes

Primary

MeasureTime frame
Eradication rates of Helicobacter pylori;

Secondary

MeasureTime frame
adverse events;compliance;

Countries

China

Contacts

Public ContactYan Tianlian

The First Affiliated Hospital, Zhejiang University School of Medicine

583195088@qq.com+86 134 8638 8649

Outcome results

None listed

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