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A multicenter randomized controlled study of a first-line eradication of Helicobacter pylori with a combination of vonoprazan and minocycline

A multicenter randomized controlled study of a first-line eradication of Helicobacter pylori with a combination of vonoprazan and minocycline

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102441
Enrollment
Unknown
Registered
2025-05-14
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Helicobacter pylori infection

Interventions

Vonoprazan-minocycline combination:Treatment plan:Vonoprazan 20mg bid + Minocycline 0.1g bid for 14 days
Vonoprazan-amoxicillin combination:Treatment plan:Vonoprazan 20mg bid +Amoxicillin 1g tid for 14 days

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-75 years old, male or female. 2. Positive C13 or C14 breath test within one month. 3. Meet the indications for the eradication of Hp as recommended by the "Sixth National Consensus Report on the Management of Helicobacter pylori Infection and are willing to receive Hp eradication therapy. 4. No history of Hp eradication therapy. 5. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. patients allergic to the drugs used in this study; 2. use of P-CAB, PPI, H2 receptor antagonist, antibiotics bismuth, probiotics, etc. within 1 month before treatment; 3. women who are pregnant or breastfeeding, and patients planning for pregnancy during the study period; 4. use of non-steroidal anti-inflammatory drugs, glucocorticoids, anticoagulants during the study period; 5. the presence of severe concomitant affecting the evaluation of this study, such as heart disease, pulmonary disease, liver disease, renal disease, metabolic disease, mental disease, malignant tumor, etc.; 6. patients who are difficult to follow up or have other factors affecting compliance.

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori eradication rate;

Secondary

MeasureTime frame
Incidence of adverse reactions;Drug adherence;

Countries

China

Contacts

Public ContactFeng Huang

The First Affiliated Hospital of Soochow University

nancyfh@163.com+86 158 5016 5709

Outcome results

None listed

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