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Efficacy Observation of Minocycline-Containing Regimen in the Treatment of Helicobacter pyloriInfection?

Efficacy Observation of Minocycline-Containing Regimen in the Treatment of Helicobacter pyloriInfection?

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122365
Enrollment
Unknown
Registered
2026-04-13
Start date
2025-02-07
Completion date
Unknown
Last updated
2026-04-20

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 VAMB:Vonoprazan + Amoxicillin+Minocycline+bismuth
Group VM:Vonoprazan + Minocycline

Sponsors

People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, Department of Gastroenterology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Adult patients aged 18–70 years;?? 2.Patients with newly diagnosed active Helicobacter pylori(Hp) infection confirmed by either ¹4C-urea breath test (UBT) or histopathological examination;?**? 3.Patients who have not taken potassium-competitive acid blockers (P-CABs), proton pump inhibitors (PPIs), H2-receptor antagonists, hydrotalcite, bismuth preparations, sucralfate, or misoprostol within the past 2 weeks;?? 4.Patients who have not received antibiotics or antibacterial traditional Chinese medicines (e.g., Jinghua Weikang, Moro Dan, berberine) within the past 4 weeks.?

Exclusion criteria

Exclusion criteria: 1. Patients who are intolerant to or allergic to any drug in the study; 2. Female patients who are pregnant, breastfeeding, or planning pregnancy; 3. Recent history of gastrointestinal haemorrhage, obstruction, perforation, tumours, or other serious organic diseases; 4. Patients with severe cardiac, hepatic, or renal insufficiency, or compromised immunity; 5. Patients with psychiatric disorders, psychological impairments, or inability to cooperate with research personnel. 6. Lack of informed consent.

Design outcomes

Primary

MeasureTime frame
Eradication rates;

Secondary

MeasureTime frame
Adverse event;Compliance;

Countries

China

Contacts

Public ContactSheng juan,Hu

People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, Department of Gastroenterology

hsj.judy@163.com+86 138 9500 5551

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026