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A randomized controlled trial of increasing the dose or frequency of tegoprazan combined with amoxicillin for the eradication of Helicobacter pylori in treatment-naive patients

A randomized controlled trial of increasing the dose or frequency of tegoprazan combined with amoxicillin for the eradication of Helicobacter pylori in treatment-naive patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105939
Enrollment
Unknown
Registered
2025-07-15
Start date
2025-07-15
Completion date
Unknown
Last updated
2025-07-21

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:Tegoprazan 100mg twice a day was taken after breakfast and dinner Amoxicillin 1000mg 3 times/day after breakfast, lunch and dinner
Group b:Tegoprazan 50mg three times/day was taken after breakfast and dinner Amoxicillin 1000mg 3 times/day after breakfast, lunch and dinner

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18-70 years old, male or female; (2) Patients were Helicobacter pylori positive by urea breath test; (3) patients with initial treatment of Helicobacter pylori; (4) Patients or their legal representatives signed informed consent, understood and agreed to follow the study requirements.

Exclusion criteria

Exclusion criteria: (1) Use of PPIs, P-CABs, antibiotics, H2-receptor antagonists, bismuth, probiotics, or herbal medicines within 4 weeks before enrollment; (2) Pregnancy, lactation, or plans for pregnancy during the study; (3) Concurrent use of NSAIDs, corticosteroids, anticoagulants, or alcohol abuse; (4) Allergy to study medications; (5) Severe comorbidities (e.g., hepatic, cardiac, renal diseases, malignancies, psychiatric disorders); (6)History of gastric or esophageal surgery; (7)Participation in other clinical trials within the past 3 months; (8)Inability to complete follow-up or poor compliance.

Design outcomes

Primary

MeasureTime frame
Comparison of helicobacter pylori eradication rate;

Secondary

MeasureTime frame
Comparison of compliance;Factors influencing eradication rate;

Countries

China

Contacts

Public ContactDekui Zhang

Lanzhou University Second Hospita

sczdk1972@163.com+86 139 0931 8616

Outcome results

None listed

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