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Clinical Trials/NCT00520949
NCT00520949
Completed
Not Applicable

Quadruple Therapy Using Esomeprazole, Colloidal Bismuth Subcitrate, Amoxicillin-Clavulanate, and Furazolidone in Patients Who Failed to Eradicate H. Pylori With Triple Therapy

Aga Khan University1 site in 1 country176 target enrollmentOctober 2006

Overview

Phase
Not Applicable
Intervention
Augmentin (Amoxicillin-clavulanic)
Conditions
Treatment of Helicobacter Pylori
Sponsor
Aga Khan University
Enrollment
176
Locations
1
Primary Endpoint
Eradication of H. pylori infection resistant to triple therapy.
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

Triple therapy, a combination of proton pump inhibitor with two antibiotics, is the gold standard for anti-Helicobacter pylori treatment. Usual antibiotics are clarithromycin, and either amoxicillin or one of the nitroimidazoles (metronidazole). However, there is an increasing evidence of H. pylori resistance to classical triple therapy. Another reason for this failure being low patient compliance with treatment. A regimen useful in one geographical area may not be effective or practical in another area. The aim of this study was to eradicate H. pylori infection resistant to triple therapy, establish the efficacy and safety of a 14-day therapeutic regimen to eradicate of H. pylori in patients who have failed with the classical triple therapy (omeprazole, clarithromycin and amoxicillin) given for 14 days.

Registry
clinicaltrials.gov
Start Date
October 2006
End Date
June 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Informed consent given by the patient
  • Patients known to have H. pylori infection diagnosed by histopathology, rapid urease test and urea breath test
  • Failure to respond to classical triple regime of amoxicillin 1gram, clarithromycin 500mg and omeprazole 20mg twice a day for 10-14 days as documented by repeat urea breath test done one month after eradication therapy

Exclusion Criteria

  • Evidence of any malignancy, gastric outlet syndrome, history of gastric surgery, chronic liver disease, severe chronic renal failure, or any major co-morbidity.
  • known or suspected hypersensitivity to the medication used in the study

Arms & Interventions

Quadruple Therapy

Intervention: Augmentin (Amoxicillin-clavulanic)

Quadruple Therapy

Intervention: Furoxone (furazolidone)

Quadruple Therapy

Intervention: Cebes (colloidal bismuth subcitrate)

Quadruple Therapy

Intervention: Esso (esomeprazole)

Outcomes

Primary Outcomes

Eradication of H. pylori infection resistant to triple therapy.

Time Frame: 6 weeks

Secondary Outcomes

  • Safety of the quadruple therapy(6 weeks)

Study Sites (1)

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