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Vonoprazan-Doxycycline Dual Therapy Versus Bismuth-Containing Doxycycline-Furazolidone Quadruple Therapy as Rescue Treatment for Helicobacter pylori: A Prospective, Multicenter, Open-Label, Randomized Controlled Trial

Vonoprazan-Doxycycline Dual Therapy Versus Bismuth-Containing Doxycycline-Furazolidone Quadruple Therapy as Rescue Treatment for Helicobacter pylori: A Prospective, Multicenter, Open-Label, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115106
Enrollment
Unknown
Registered
2025-12-22
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

helicobacter pylori infection

Interventions

Group B:Doxycycline dual therapy
Group A:Bismuth quadruple solution

Sponsors

NanJing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18-65 years old; 2. Patients diagnosed as positive for Helicobacter pylori by 13C-UBT or 14C-UBT; 3. Patients who have previously received dual therapy containing amoxicillin to eradicate Hp; 4. Voluntarily join this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergic to the studied drugs (such as furazolidone, vonoprazan, doxycycline, etc.); 2. Identify patients with active peptic ulcers; 3. Patients who have not received Helicobacter pylori eradication treatment before; 4. Patients who have previously received bismuth quadruple therapy containing furazolidone, tetracycline and tetracycline antibiotics to eradicate Hp; 5. Antibiotics and bismuth agents should be used 4 weeks before the start of the study treatment, and histamine H2 receptor antagonists or PPIs should be used 2 weeks before the start. 6. Use adrenal cortical hormones, non-steroidal anti-inflammatory drugs, anticoagulants, barbiturates, phenytoin or carbamazepine and other drugs; 7. History of esophageal or gastric surgery; 8. Pregnant and lactating women; 9. Alcoholism; 10. Suffering from serious concomitant diseases, such as liver diseases, cardiovascular diseases, lung diseases, and kidney diseases; 11. Those with liver dysfunction caused by hepatitis, fatty liver and other reasons; 12. Gastric mucosa-associated lymphoid tissue lymphoma (MALT), malignant tumor diseases.

Design outcomes

Primary

MeasureTime frame
Hp eradication rate;

Secondary

MeasureTime frame
Safety observation;Fecal genetic testing;

Countries

China

Contacts

Public ContactZhangZhenyu

NanJing First Hospital

zzy6565@sina.com+86 25 52271000

Outcome results

None listed

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