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Molecular Detection of Antibiotic Resistance and H Pylori Eradication (HELICOSTIC)

Primary Purpose

Helicobacter Pylori Infection

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Molecular detection of antibiotic resistance
standard triple therapy (PPI, amoxicillin, clarithromycin, metronidazole)
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Helicobacter Pylori Infection focused on measuring Helicobacter pylori, Diagnostic molecular testing, Antibiotic resistance, Treatment protocols

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Henri Mondor Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Helicobacter pilory triple treatment

Helicobacter pilori standard recommended treatment

Arm Description

Triple treatment on this arm is based on results of molecular detection of resistance to antibiotics

H.Pylori Eradication rate with empirical treatment

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Comparative cost of the two strategies

Full Information

First Posted
July 21, 2010
Last Updated
November 7, 2013
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT01168063
Brief Title
Molecular Detection of Antibiotic Resistance and H Pylori Eradication
Acronym
HELICOSTIC
Official Title
Medico-economic Evaluation of a Therapeutic Strategy Based on Molecular Detection of Antibiotic Resistance in the Management of H Pylori Infection
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
March 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Helicobacter Pylori Infection
Keywords
Helicobacter pylori, Diagnostic molecular testing, Antibiotic resistance, Treatment protocols

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1386 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Helicobacter pilory triple treatment
Arm Type
Experimental
Arm Description
Triple treatment on this arm is based on results of molecular detection of resistance to antibiotics
Arm Title
Helicobacter pilori standard recommended treatment
Arm Type
Active Comparator
Arm Description
H.Pylori Eradication rate with empirical treatment
Intervention Type
Drug
Intervention Name(s)
Molecular detection of antibiotic resistance
Other Intervention Name(s)
Helicobacter Molecular detection of resistance to clarithromycin and quinolones, Use of triple therapy base on antibiotics resistances (PPI,amoxicillin,clarithromycin, metronidazole)
Intervention Description
Helico DR®, triple therapy (Proton Pomp Inhibitor (PPI), amoxicillin, clarithromycin, metronidazole)
Intervention Type
Drug
Intervention Name(s)
standard triple therapy (PPI, amoxicillin, clarithromycin, metronidazole)
Other Intervention Name(s)
Standard triple therapy (PPI, amoxicillin, clarithromycin, metronidazole ….)
Intervention Description
2 lines of treatments : 1) PPI + Amoxicillin + Clarithromycin for 7 days 1) PPI + Amoxicillin + Metronidazole for 14 days
Primary Outcome Measure Information:
Title
H. pylori eradication rate (at 3months according to the two strategies: empirical treatment versus treatment guided by molecular detection of antibiotic resistance)
Description
at 3 months according to the two strategies: empirical treatment versus treatment guided by molecular detection of antibiotic resistance
Time Frame
at 3 months
Secondary Outcome Measure Information:
Title
Comparative cost of the two strategies
Time Frame
at 6 months according to the two strategies

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Charles Delchier, PU-PH
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Henri Mondor Hospital
City
Creteil
ZIP/Postal Code
94010
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
10086658
Citation
Breuer T, Graham DY. Costs of diagnosis and treatment of Helicobacter pylori infection: when does choosing the treatment regimen based on susceptibility testing become cost effective? Am J Gastroenterol. 1999 Mar;94(3):725-9. doi: 10.1111/j.1572-0241.1999.00943.x.
Results Reference
result
PubMed Identifier
31257067
Citation
Delchier JC, Bastuji-Garin S, Raymond J, Megraud F, Amiot A, Cambau E, Burucoa C; HELICOSTIC Study Group. Efficacy of a tailored PCR-guided triple therapy in the treatment of Helicobacter pylori infection. Med Mal Infect. 2020 Sep;50(6):492-499. doi: 10.1016/j.medmal.2019.06.001. Epub 2019 Jun 27.
Results Reference
derived

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Molecular Detection of Antibiotic Resistance and H Pylori Eradication

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