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Third-line H. pylori eradication therapy with sitafloxacin-including regimen

Third-line H. pylori eradication therapy with sitafloxacin-including regimen - H. pylori eradication therapy with sitafloxacin-including regimen

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001558
Enrollment
30
Registered
2008-12-11
Start date
2008-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients with H. pylori eradication failure after the second-line regimen

Interventions

H. pylori eradication therapy with sitafloxacin-including regimen

Sponsors

DIvision of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients with H. pylori eradication failure after obtaining the informed consent.

Exclusion criteria

Exclusion criteria: penicillin or quinolone allergy rabeprazole allergy severe liver dysfunction, renal dysfunction pregnancy or possibly pregnancy cases with unsuitable recognition by doctors

Design outcomes

Primary

MeasureTime frame
Eradication rate of H. pylori by sitafloxacin-including regimen

Secondary

MeasureTime frame
MIC of sitafloxacin, gyrA mutation of H. pylori

Countries

Japan

Contacts

Public ContactHidekazu Suzuki

Keio University School of Medicine Division of Gastroenterology and Hepatology, Department of Internal Medicine

hsuzuki@sc.itc.keio.ac.jp03-5363-3914

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026