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Efficacy study of tegoprazan dual therapy and bismuth containing quadruple therapy for eradication of Helicobacter pylori

Efficacy study of tegoprazan dual therapy and bismuth containing quadruple therapy for eradication of Helicobacter pylori

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089417
Enrollment
Unknown
Registered
2024-09-09
Start date
2024-09-16
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Helicobacter pylori infection

Interventions

intervention group:Tegoprazan 50mg twice a day and amoxicillin 1.0g three times a day for 10 days
control group:Rabeprazole 20mg twice a day, amoxicillin 1.0g twice a day, Furazolidone 0.1g twice a day, colloidal bismuth pectin 200mg twice a day for 10 days

Sponsors

Chengdu Xinhua Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age range from 18 to 75 years old, both male and female are welcome; 2. Clearly diagnose newly diagnosed patients with HP; 3. 13 C-urea breath test (13 C-UBT) or 14 C-urea breath test (14 C-UBT) positive; 4. The rapid urease test of gastroscopy biopsy was positive; 5.Confirmed by histopathological examination; 6.Monoclonal antibody fecal antigen test positive.

Exclusion criteria

Exclusion criteria: 1. Aged 75 years; 2. Pregnancy, lactation, serious concomitant diseases, malignant tumors, allergic study drugs, severe ulcer bleeding or perforation, history of upper gastrointestinal surgery, previous treatment with H. pylori, PPI or antibiotics within 4 weeks. 3. All patients underwent their first HP eradication treatment, and those who failed the first treatment and required remedial treatment, as well as those allergic to amoxicillin, were not included in the study.

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori eradication rate;

Secondary

MeasureTime frame
adverse reaction;adherence;

Countries

China

Contacts

Public ContactHuang Yuanlong

Chengdu Xinhua Hospital

359985006@qq.com+86 151 0285 7874

Outcome results

None listed

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