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Efficacy and safety of vonoprazan–minocycline dual therapy for refractory Helicobacter pylori rescue treatment compared with furazolidone containing bismuth quardruple therapy

Efficacy and safety of vonoprazan–minocycline dual therapy for refractory Helicobacter pylori rescue treatment compared with furazolidone containing bismuth quardruple therapy

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084535
Enrollment
Unknown
Registered
2024-05-20
Start date
2024-05-23
Completion date
Unknown
Last updated
2024-05-27

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-minocycline dual therapy

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years; 2. 13C urea breath test is positive; 3. Meet the indications for Helicobacter pylori eradication (according to the Sixth National Consensus Report on the Treatment of Helicobacter pylori Infection); 4. Patients who have failed to take the quadruple regimen for 10-14 days at least twice in the past and need to undergo gastroscopy; 5. Those who have received Helicobacter pylori eradication therapy in the past need to stop the drug for more than 3 months before entering the group.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to the drugs used in the eradication program; 2. Patients with a history of ß-lactam allergy, allergic constitution and allergic reaction. 3. After gastric surgery; 4. Pregnant and lactating women; 5. Taking glucocorticoids, non-steroidal drugs, anticoagulants; 6. Patients with low body weight (weight less than 40kg), patients with severe liver, kidney, cardiac insufficiency, malignant tumor, and cerebrovascular disease. 7. Patients with uncontrolled acute disease.

Design outcomes

Primary

MeasureTime frame
13C urea breath test;compliance;

Secondary

MeasureTime frame
adverse effects;

Countries

China

Contacts

Public ContactWeihong Wang

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