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Molecular Detection of Antibiotic Resistance and H Pylori Eradication

Medico-economic Evaluation of a Therapeutic Strategy Based on Molecular Detection of Antibiotic Resistance in the Management of H Pylori Infection

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01168063
Acronym
HELICOSTIC
Enrollment
1386
Registered
2010-07-22
Start date
2010-02-28
Completion date
2013-03-31
Last updated
2013-11-08

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

Conditions

Helicobacter Pylori Infection

Keywords

Helicobacter pylori, Diagnostic molecular testing, Antibiotic resistance, Treatment protocols

Brief summary

H pylori eradication failure with recommended triple therapy is mainly related to antibiotic resistance. However,IN VITRO culture of H pylori is uneasy and is not performed in routine practice. A molecular test of antibiotic resistance easy to perform is now available. The aim of the study was to compare eradication rates obtained with the standard treatment and with a treatment guided by the results of the molecular detection of antibiotic resistance.

Detailed description

At the present time, H pylori infection is treated with a standard triple therapy. Treatment of naïve patients with triple therapy ( PPI+amoxicillin+clarithromycin for 7 days) markedly decreased last years to reach 70% due to a clarithromycin resistance rate about 20% in France. In case of failure, the recommended second line treatment (PPI+amoxicillin+metronidazole for 14 days) gives a success rate of 60%. However, as culture is uneasy and is only possible in specialised labs sensitivity to antibiotics is not currently studied before treatment. The aim of the study was to evaluate clinical and medico-economic benefit of the molecular detection of antibiotic resistance in order to guide the treatment. The test is performed after DNA extraction from biopsy specimens taken at gastroscopy allowing rapid detection of H pylori and clarithromycin or quinolone resistance. Patients with bacteriologically proven H pylori infection will be randomly allocated to either empirical usual treatment with PPI , amoxicillin 1g, clarithromycin 500 mg X 2 /day for 7 days in naïve patients and PPI, amoxicillin 1g,metronidazole 500 mg X 2 /day for 14 days in patients who failed a first line treatment , or to treatment guided by the molecular test: PPI , amoxicillin 1g, clarithromycin 500 mg X 2 /day for 7 days in case of sensitivity to clarithromycin.In case of resistance to clarithromycin, quinolone should be given and in case of resistance to quinolone clarithromycin should be given. In case of resistance to both antibiotics metronidazole should be given. Eradication will be assessed by performing 4 weeks after the completion of treatment with Urea Breath Test.

Interventions

Helico DR®, triple therapy (Proton Pomp Inhibitor (PPI), amoxicillin, clarithromycin, metronidazole)

DRUGstandard triple therapy (PPI, amoxicillin, clarithromycin, metronidazole)

2 lines of treatments : 1\) PPI + Amoxicillin + Clarithromycin for 7 days 1\) PPI + Amoxicillin + Metronidazole for 14 days

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* H pylori infection bacteriologically confirmed * Age \> 18 years * Naïve patient or one failure of the first line recommended treatment * Patient referred to one out of the centres participating in the study

Exclusion criteria

* H pylori positive patient with at least failure of two lies of treatment * patients with previous adverse event with PPI, amoxicillin, clarithromycin, levofloxacin or metronidazole * PPI or antibiotic treatment in progressor stopped for less than 4 weeks * patient with other severe sickness

Design outcomes

Primary

MeasureTime frameDescription
H. pylori eradication rate (at 3months according to the two strategies: empirical treatment versus treatment guided by molecular detection of antibiotic resistance)at 3 monthsat 3 months according to the two strategies: empirical treatment versus treatment guided by molecular detection of antibiotic resistance

Secondary

MeasureTime frame
Comparative cost of the two strategiesat 6 months according to the two strategies

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026