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NCT Number: NCT02175901

Amoxicillin/Metronidazole Based Quadruple Therapy for Helicobacter Pylori Eradication

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Shanghai Renji Hospital, Shanghai Jiao-Tong University School of Medicine

Shanghai, Shanghai Municipality, 200127, China

About this study

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 H. 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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Lansoprazole

Drug

antisecretory drug of each quadruple therapy

Other names: proton pump inhibitor

Bismuth Potassium Citrate

Drug

one component of each quadruple therapy

Other names: Bismuth

Amoxicillin

Drug

antibiotic of each quadruple therapy

Other names: antibiotic

Metronidazole

Drug

antibiotic of the amoxicillin/metronidazole-based quadruple therapy

Other names: antibiotic

Clarithromycin

Drug

antibiotic of the amoxicillin/clarithromycin-based quadruple therapy

Other names: antibiotic

Primary outcomes

  1. Eradication rate of Helicobacter pylori

    Time frame: 2 months

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

Secondary outcomes

  1. Frequency of side effects of each treatment

    Time frame: 2 months

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

Other outcomes

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

    Time frame: 2 months

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

Sponsors and collaborators

Lead sponsor

Shanghai Jiao Tong University School of Medicine

Other

Registry information

Official study 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

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jun 26, 2014
Registry last updated
Feb 3, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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