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Helicobacter pylori eradication with minocycline-containing double/quadruple therapy:prospective, multicenter, open-label, randomized controlled clinical study

Helicobacter pylori eradication with minocycline-containing double/quadruple therapy:prospective, multicenter, open-label, randomized controlled clinical study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089850
Enrollment
Unknown
Registered
2024-09-18
Start date
2024-09-10
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Helicobacter pylori infection

Interventions

14d-VA:Amoxicillin-containing 14-day dual therapy
14d-VM:Minocycline-containing 14-day dual therapy
14d-VBAM:14-day regimen of bismuth quadruple therapy with minocycline
7d-VBAM:7-day regimen of bismuth quadruple therapy with minocycline

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age>= 18 years and = 6 or 14C>= 150); (3) No previous Helicobacter pylori eradication therapy; (4) Patients were informed and agreed to participate in this trial.

Exclusion criteria

Exclusion criteria: (1) Pregnant or breastfeeding women, or patients who plan to have children during the study; (2) Patients who have taken acid inhibitors, H2-receptor blockers, bismuth or antibiotics within 4 weeks before treatment; (3) Patients with serious problems in other organs (such as liver disease, cardiovascular disease, lung disease, kidney disease, metabolic disease, malignant tumors, neuropsychiatric diseases, etc.); (4) Patients who are allergic to any of the drugs used; (5) Patients who are unable to express their complaints correctly, such as those with mental illness, severe neurosis and inability to cooperate; (6) Any other health condition assessed by the doctor as not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
The eradication rate of Helicobacter pylori;

Secondary

MeasureTime frame
Adverse reactions;

Countries

China

Contacts

Public ContactLi Hong

West China Hospital of Sichuan University

anhong99999@163.com+86 28 8542 2650

Outcome results

None listed

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