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Study for the eradication therapy of esomeprazole, bismuth agent, metronidazole combined with tetracycline or amoxicillin in native patients with helicobacter pylori infection

Study for the eradication therapy of esomeprazole, bismuth agent, metronidazole combined with tetracycline or amoxicillin in native patients with helicobacter pylori infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024964
Enrollment
Unknown
Registered
2019-08-05
Start date
2019-08-15
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Helicobacter pylori infection

Interventions

quadruple therapy containing tetracycline and bismuth agent:quadruple therapy containing tetracycline and bismuth agent
quadruple therapy containing amoxicillin and bismuth agent:quadruple therapy containing amoxicillin and bismuth agent

Sponsors

Department of Gastroenterology, Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Consecutive patients with dyspepsia who are referred to our hospital for upper endoscopy; 2. HP RUT and W-S staining positive; 3. Never received treatment for H. pylori infection; 4. Aged greater than or equal to 18 years; 5. Willing and available for participation this study.

Exclusion criteria

Exclusion criteria: 1. Taking any drug which could influence the study results such as PPI, H2-receptor blockers, bismuth salts and antibiotics in the previous 4 weeks; 2. Gastrointestinal malignancy; 3. Zollinger-Ellison syndrome; 4. Previous gastric and esophageal surgeries; 5. Severe concomitant cardiovascular, respiratory, renal, hepatic, hematological, neurological, endocrine or psychiatric diseases; 6. History of allergy to any of the drugs used in the study; 7. Pregnancy or lactation; 8. Any other clinically significant medical condition that could increase risk of side effects.

Design outcomes

Primary

MeasureTime frame
eradication rate;

Secondary

MeasureTime frame
Adverse event rate;compliance;

Countries

China

Contacts

Public ContactZhiqiang Song

Peking University Third Hospital

18910192576@163.com+86 18910192576

Outcome results

None listed

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