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Clinical Trials/JPRN-UMIN000006483
JPRN-UMIN000006483CompletedPhase 3

Double blind-randomized controlled trial for the efficacy of third line H. pylori eradication therapy between sitafloxacin-including regimen and sitafloxacin and metronidazole-including regimen - Double blind-randomized controlled trial for the efficacy of third line H. pylori eradication therapy

Keio University School of Medicine0 sites200 target enrollmentStarted: November 1, 2012Last updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
200

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to ot applicable (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1. Patients with allergy for quinolones 2. Patients with allergy for PPIs 3. Patients with severe liver injury and/or severe renal damage 4. Pregnancy or possible pregnancy 5. Patients who were recognized as inappropriate for entry

Investigators

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