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Evaluation of the efficacy of berberine combined with Vonoprazan and amoxicillin for eradication of Helicobacter pylori

Evaluation of the efficacy of berberine combined with Vonoprazan and amoxicillin for eradication of Helicobacter pylori

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077074
Enrollment
Unknown
Registered
2023-10-27
Start date
2023-10-31
Completion date
Unknown
Last updated
2023-10-30

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 A:Berberine hydrochloride tablets 200mg + Vonoprazan fumarate tablets 20mg + amoxicillin capsule 1g, berberine hydrochloride tablets 3 times a day and all the rest of the medicines were given tw
Group B:Berberine hydrochloride tablets 300mg + Vonoprazan fumarate tablets 20mg + amoxicillin capsule 1g, berberine hydrochloride tablets 3 times a day, and all the rest of the medicines were given t
Group C:Colloidal bismuth pectin capsules 200mg + Rabeprazole sodium enteric-coated tablets 20mg + amoxicillin capsules 1g + clarithromycin tablets 0.5g, all medications were given twice a day for 14

Sponsors

Qianxinan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with a positive 13C/14C urea breath test and gastroscopy; with gastrointestinal symptoms such as epigastric pain, bloating, nausea, heartburn, acid reflux, and belching; no history of psychiatric disorders, and no communication barriers with the investigator; between 18 and 70 years of age; and willingness to be eradicated and signing of an informed consent form.

Exclusion criteria

Exclusion criteria: Hypersensitivity to the study drug; severe cardiac, pulmonary, hepatic, or renal disease;Prior treatment with antibiotics, acid suppressants, or bismuth within 4 weeks; children, pregnant women, and nursing mothers; glucose-6-phosphate dehydrogenase deficiency; patients with incomplete information.

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori eradication rate;

Secondary

MeasureTime frame
Clinical symptom relief rate;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactJun Guo

Qianxinan People's Hospital

gjun1973@163.com+86 131 5075 3235

Outcome results

None listed

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