Amoxicillin/Metronidazole Based Quadruple Therapy for Helicobacter Pylori Eradication

Sponsor
Shanghai Jiao Tong University School of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT02175901
Collaborator
(none)
215
1
2
6
35.6

Study Details

Study Description

Brief Summary

No trial has examined the the efficacy of amoxicillin and metronidazole based quadruple therapy for Helicobacter pylori treatment. The study aims to compare the effectiveness and safety of 14-day amoxicillin-/metronidazole-based quadruple regiment and classical quadruple regiment for Helicobacter pylori eradication.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Helicobacter pylori is the most successful human pathogen infecting an estimated 50% of the global population. It is a common and potentially curable cause of dyspepsia and peptic ulcer disease. Eradication in patients with peptic ulcer or even functional or non-investigated dyspepsia is a cost effective approach.

Most Consensus Conferences and Clinical Guidelines recommend the prescription of a triple therapy including a proton pump inhibitor (PPI) and clarithromycin with either amoxicillin or metronidazole, as first-line treatment. However, the effectiveness of these triple-therapy regimens seems to have diminished over time, largely as a result of emerging resistance of the organism to clarithromycin. Due to the low efficacy achieved with these treatments, they have been deemed as unethical comparators in clinical trials. As antimicrobial resistance becomes more prevalent worldwide, treatment failure rates are likely to continue increasing, suggesting that new regimens for H pylori eradication must be sought.

Bismuth-containing quadruple therapies have been used widely in H. pylori therapy with many permutations of doses and durations and with variable results. Classical bismuth-based quadruple therapy containing a PPI, bismuth, tetracycline and metronidazole has been recommended as the first-line treatment by the Maastricht IV Consensus Conference report and

  1. pylori Study Group of Chinese Society of Gastroenterology. But this regiment has high rate of side effects because of tetracycline. Standard triple therapy-based, bismuth-containing quadruple Therapy is also an alternative. Though addition bismuth and prolonging treatment duration can overcome H. pylori resistance to clarithromycin, its use as a first-line treatment is limited in areas of high clarithromycin resistance.

Amoxicillin has low resistance rate as well as low percentage of side effects. The combination of amoxicillin and metronidazole in bismuth-containing quadruple therapy may be a better choice, which can avoid clarithromycin resistance and reduce side effects. Therefore, we will do a randomized trial to compare the eradication rate of 14-day amoxicillin and metronidazole based bismuth-containing quadruple therapy with amoxicillin and clarithromycin based quadruple therapy for Helicobacter pylori infection.

Study Design

Study Type:
Interventional
Actual Enrollment :
215 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective, Randomized Controlled Trial Comparing Amoxicillin and Metronidazole Based Bismuth-containing Quadruple Therapy With Amoxicillin and Clarithromycin Based Quadruple Therapy for First-line Helicobacter Pylori Eradication
Study Start Date :
Jul 1, 2014
Actual Primary Completion Date :
Jan 1, 2015
Actual Study Completion Date :
Jan 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Amoxicillin/metronidazole

Amoxicillin/metronidazole-based quadruple therapy for 14 days: Lansoprazole 30mg bid, Bismuth Potassium Citrate 220mg bid, amoxicillin 1000mg bid, Metronidazole 400mg qid

Drug: Lansoprazole
antisecretory drug of each quadruple therapy
Other Names:
  • proton pump inhibitor
  • Drug: Bismuth Potassium Citrate
    one component of each quadruple therapy
    Other Names:
  • Bismuth
  • Drug: Amoxicillin
    antibiotic of each quadruple therapy
    Other Names:
  • antibiotic
  • Drug: Metronidazole
    antibiotic of the amoxicillin/metronidazole-based quadruple therapy
    Other Names:
  • antibiotic
  • Active Comparator: Amoxicillin/clarithromycin

    Amoxicillin/clarithromycin-based quadruple therapy for 14 days: Lansoprazole 30mg bid, Bismuth Potassium Citrate 220mg bid, Amoxicillin 1000mg bid, Clarithromycin 500mg bid

    Drug: Lansoprazole
    antisecretory drug of each quadruple therapy
    Other Names:
  • proton pump inhibitor
  • Drug: Bismuth Potassium Citrate
    one component of each quadruple therapy
    Other Names:
  • Bismuth
  • Drug: Amoxicillin
    antibiotic of each quadruple therapy
    Other Names:
  • antibiotic
  • Drug: Clarithromycin
    antibiotic of the amoxicillin/clarithromycin-based quadruple therapy
    Other Names:
  • antibiotic
  • Outcome Measures

    Primary Outcome Measures

    1. Eradication rate of Helicobacter pylori [2 months]

      Access eradication rate of H. pylori by intention to treat (ITT) and per-protocol (PP) analysis in each treatment group

    Secondary Outcome Measures

    1. Frequency of side effects of each treatment [2 months]

      Score side effects as mild, moderate or severe according to their influence on daily activities

    Other Outcome Measures

    1. Minimal inhibitory concentrations (MIC) of antibiotics against each helicobacter pylori clinical isolate [2 months]

      Determine MIC of amoxicillin, clarithromycin, and metronidazole by the twofold agar dilution method.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Participants with non-investigated/functional dyspepsia or scarred peptic ulcer with indication of H pylori eradication treatment

    • Ability and willingness to participate in the study and to sign and give informed consent

    • confirmed H pylori infection by at least one of the following methods: C13-urea breath test, histology, rapid urease test or bacterial culture.

    Exclusion Criteria:
    • patients with peptic ulcer

    • previous H. pylori eradication therapy

    • Age below 18 years

    • major systemic diseases

    • previous gastric surgery

    • pregnancy or breastfeeding

    • allergy to any of the study drugs

    • receipt of anti-secretory therapy, antibiotics or bismuth salts 4 weeks prior to inclusion

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Shanghai Renji Hospital, Shanghai Jiao-Tong University School of Medicine Shanghai Shanghai China 200127

    Sponsors and Collaborators

    • Shanghai Jiao Tong University School of Medicine

    Investigators

    • Principal Investigator: Hong Lu, M.D., RenJi Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Hong Lu, MD, Professor of GI Division, Shanghai Jiao Tong University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT02175901
    Other Study ID Numbers:
    • rjkls2014006
    First Posted:
    Jun 26, 2014
    Last Update Posted:
    Feb 3, 2015
    Last Verified:
    Feb 1, 2015
    Keywords provided by Hong Lu, MD, Professor of GI Division, Shanghai Jiao Tong University School of Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 3, 2015