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Different quadruple therapies for Helicobacter pylori infection: a randomised, parallel trial

Different quadruple therapies for Helicobacter pylori infection: a randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003256
Enrollment
Unknown
Registered
2013-03-28
Start date
2013-05-01
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

A:PPI+ bismuth+amoxicillin,+clarithromycin
B:PPI+ bismuth+amoxicillin+ levofloxacin
C:PPI+amoxicillin+ levofloxacin

Sponsors

First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients were eligible for recruitment if they were aged from 20 to 65 years old and were dignosed as duodenal ulcer or chronic gastritis.Meantime they should have documented H pylori infection and never have previous eradication treatment for H pylori.

Exclusion criteria

Exclusion criteria: (1) use of antibiotics, bismuth, H2RA and PPI, anticoagulant drugs in the past 4 weeks: (2) histor y of gastrectomy,gastric malignancy, including adenocarcinoma and lymphoma; (3) active upper gastrointestinal bleeding within the previous 1 week; (4) pregnant or lactating women; (5) At the same time there are other serious diseases such as severe liver disease, heart disease (including block, chronic heart failure), kidney disease, cerebrovascular disease, cancer and alcoholism disorders affecting the evaluation of this study; (6) allergic reaction to the drug used in this study; (7) during treatment need to take the metal preparations (metal preparations may chelation with levofloxacin, except bismuth); (8) participate in other drug studies in the past 3 months before: (9) the patient who can not properly express their own complaints, such as psychosis, severe neurosis, not collaborators.

Design outcomes

Primary

MeasureTime frame
eradication rate;

Contacts

Public ContactGuoxin Zhang
guoxinz@njmu.edu.cn+86 13951913128

Outcome results

None listed

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