Skip to content

Amoxicillin/Metronidazole Based Quadruple Therapy for Helicobacter Pylori Eradication

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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02175901
Enrollment
215
Registered
2014-06-26
Start date
2014-07-31
Completion date
2015-01-31
Last updated
2015-02-03

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

Conditions

Dyspepsia, Peptic Ulcer

Keywords

helicobacter pylori eradication, antibiotic

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.

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 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.

Interventions

DRUGLansoprazole

antisecretory drug of each quadruple therapy

DRUGBismuth Potassium Citrate

one component of each quadruple therapy

DRUGAmoxicillin

antibiotic of each quadruple therapy

DRUGMetronidazole

antibiotic of the amoxicillin/metronidazole-based quadruple therapy

DRUGClarithromycin

antibiotic of the amoxicillin/clarithromycin-based quadruple therapy

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
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

Design outcomes

Primary

MeasureTime frameDescription
Eradication rate of Helicobacter pylori2 monthsAccess eradication rate of H. pylori by intention to treat (ITT) and per-protocol (PP) analysis in each treatment group

Secondary

MeasureTime frameDescription
Frequency of side effects of each treatment2 monthsScore side effects as mild, moderate or severe according to their influence on daily activities

Other

MeasureTime frameDescription
Minimal inhibitory concentrations (MIC) of antibiotics against each helicobacter pylori clinical isolate2 monthsDetermine MIC of amoxicillin, clarithromycin, and metronidazole by the twofold agar dilution method.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026