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A randomized control trial exploring the eradication efficacy in naive patients with helicobacter pylori infection treated with the quadruple therapy containing amoxicillin or cefuroxime

A randomized control trial exploring the eradication efficacy in naive patients with helicobacter pylori infection treated with the quadruple therapy containing amoxicillin or cefuroxime

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006389
Enrollment
Unknown
Registered
2015-05-13
Start date
2015-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Helicobacter pylori infection

Interventions

Amoxicillin-containing quadruple therapy :Amoxicillin-containing quadruple therapy
Cefuroxime-containing quadruple therapy:Cefuroxime-containing quadruple therapy

Sponsors

Department of Gastroenterology, Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 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. Penicillin skin test negative; 4. Never received treatment for H. pylori infection; 5. Aged 20 to 70 years; 6. 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 ContactLiya ZHOU
liyazhou@medmail.com.cn+86 15611908239

Outcome results

None listed

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