European Registry on the Management of Helicobacter Pylori Infection

Sponsor
Javier P. Gisbert (Other)
Overall Status
Recruiting
CT.gov ID
NCT02328131
Collaborator
(none)
10,000
30
138
333.3
2.4

Study Details

Study Description

Brief Summary

The great diversity of regimens and treatment lines, the different efficacy of these, mostly due to the increase in bacterial antibiotic resistance and regional differences, requires a continuous critical analysis of clinical practice, evaluating systematically the efficacy and safety of the different regimens and the cost-effectiveness of the different diagnostic-therapeutic strategies. This will help in the design of an efficient and optimized treatment that will reduce number of re-treatments, diagnostic tests and the appearance of associated pathologies such as peptic ulcers, gastrointestinal bleeding and, probably, gastric cancers. Therefore, the evaluation of real clinical practice using non-interventionist registries will help to improve the design and organization of European Consensus on the management of H. pylori infection, which is the best way to establish healthcare efficiency.

Primary aim

To obtain a database registering systematically over a year a large and representative sample of routine clinical practice of European gastroenterologists in order to produce descriptive studies of the management of H. pylori infection.

Secondary aims

  1. To evaluate H. pylori infection consensus and clinical guidelines implementation in different countries.

  2. To perform studies focused on epidemiology, efficacy and safety of the commonly used treatments to eradicate H. pylori.

  3. To evaluate accessibility to healthcare technologies and drugs used in the management of

  1. pylori infection.
  1. To allow the development of partial and specific analysis by the participating researchers after approval by the Registry's Scientific Committee

Methodology Non-interventionist prospective multicentre international registry promoted by the European Helicobacter Study Group. A renowned gastroenterologist from each country was selected as Local Coordinator (30 countries). They will in turn select up to ten gastroenterologists per country that will register the routine clinical practice consultations they receive over 10 years in an electronic Case Report Form (e-CRF). Variables retrieved will include clinical, diagnostic, treatment, eradication confirmation and outcome data. The database will allow researchers to perform specific subanalysis after approval by the Scientific Committee of the study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Abstract

    Introduction: H. pylori selectively infects the human stomach mucosa, being the most prevalent chronic infection in the world. Its prevalence correlates with socioeconomic factors and it is higher in older individuals. H. pylori presence causes chronic gastritis in 100% of infected patients and is the major cause of relevant diseases such as atrophic gastritis, peptic ulcer disease and gastric cancer; it is for this reason that from a public health standpoint it is considered a high impact pathogen, responsible of a significant morbidity and mortality. Nowadays there are Consensus and Clinical Guidelines regarding the infection management at a European level and in most of the states, but no data have shown the level of implementation of these recommendations. The high costs that this infection carries both socially and to the health system require the continuous and systematic assessment of the diagnostic and treatment strategies, as well as the accessibility to diagnostic methods and most efficient drugs.

    Aim: To register the treatment, diagnosis and management strategies of H. pylori infected adult patients in the Digestive Services outpatient clinics throughout Europe.

    Methods: Non-interventionist prospective multicentre international registry promoted by the European Helicobacter Study Group. A renowned gastroenterologist from each country was selected as Local Coordinator (30 countries). They will in turn select up to ten gastroenterologists per country that will register the routine clinical practice consultations they receive over 10 years in an electronic Case Report Form (e-CRF). Variables retrieved will include clinical, diagnostic, treatment, eradication confirmation and outcome data. The database will allow researchers to perform specific subanalysis after approval by the Scientific Committee of the study.

    INTRODUCTION

    1. pylori presence causes chronic gastritis in 100% of infected patients and is the major cause of relevant diseases such as atrophic gastritis, peptic ulcer disease and gastric cancer. H. pylori eradication prevents peptic ulcer recurrence and its complications, and decreases the incidence of gastric cancer. H. pylori eradication in patients with peptic ulcer or even functional or non-investigated dyspepsia is a cost-effective strategy.

    The most common clinical manifestation of H. pylori infection is dyspepsia, a major health problem, whose prevalence reaches more than 10% among adult populations with its attendant burden of morbidity and health system costs in diagnosis and treatment. Approximately 20% to 30% of people in the community each year report chronic or recurrent dyspeptic symptoms, and consultations for dyspepsia account for up to 40% of referrals among gastroenterology outpatients, the "test-and-treat" strategy being the most cost-effective. Moreover, H. pylori is the major cause of peptic ulcer disease, causing over 90% of duodenal and 70% of gastric ulcers. Considerable evidence supports that the nature of the chronic inflammatory process driven by H. pylori is of critical importance in gastric carcinogenesis (adenocarcinoma and mucosa-associated lymphoid tissue -MALT- lymphoma). It is for that reason that the WHO's International Agency for Research on Cancer classified H. pylori as a group 1 (definite) carcinogen.

    Scientific evidence demonstrates that diagnosis and eradication of H. pylori is the most cost-effective strategy in the management of dyspepsia, peptic ulcer and gastric cancer prevention. The treatment regimens are very diverse and have changed overtime. Monotherapies and treatments with two drugs did not achieve acceptable eradication rates. The commonly recommended regimen in most Consensus Conferences is the standard triple regimen, combining two antibiotics (clarithromycin with amoxicillin or metronidazole) and a proton pump inhibitor (PPI) for 7 to 14 days. Another recommended alternative is bismuth-containing quadruple therapy (PPI, tetracycline, metronidazole and bismuth salts). In the last years, results with new and efficient rescue regimens including levofloxacin have been published. Lately, new treatments have been proposed, including non-bismuth quadruple regimens, with two main variants: the "sequential" treatment (an induction phase with PPI and amoxicillin and a second phase with PPI, clarithromycin and metronidazole) and the "concomitant" treatment (same four drugs taken altogether).

    The great diversity of regimens and treatment lines, the different efficacy of these, mostly due to the increase in bacterial antibiotic resistance and regional differences, requires a continuous critical analysis of clinical practice, evaluating systematically the efficacy and safety of the different regimens and the cost-effectiveness of the different diagnostic-therapeutic strategies. This will help in the design of an efficient and optimized treatment that will reduce number of re-treatments, diagnostic tests and the appearance of associated pathologies such as peptic ulcers, gastrointestinal bleeding and, probably, gastric cancers. Therefore, the evaluation of real clinical practice using non-interventionist registries will help to improve the design and organization of European Consensus on the management of H. pylori infection, which is the best way to establish healthcare efficiency.

    AIMS

    Primary aim To obtain a database registering systematically over a year a large and representative sample of routine clinical practice of European gastroenterologists in order to produce descriptive studies of the management of H. pylori infection.

    Secondary aims

    1. To evaluate H. pylori infection consensus and clinical guidelines implementation in different countries.

    2. To perform studies focused on epidemiology, efficacy and safety of the commonly used treatments to eradicate H. pylori.

    3. To evaluate accessibility to healthcare technologies and drugs used in the management of

    1. pylori infection.
    1. To allow the development of partial and specific analysis by the participating researchers after approval by the Registry's Scientific Committee.

    METHODS

    International multicenter prospective non-interventionist registry promoted by the European Helicobacter Study Group.

    Scientific Committee

    • Javier P. Gisbert (President)

    • Francis Megraud

    • Colm O'Morain

    • Adrian G. McNicholl

    Local Coordinators

    A list of European Countries has been selected. Included countries were those having at least ten clinical research publications in PubMed regarding H. pylori infection.

    In each country a Local Coordinator was selected based on its clinical and research activity (Table I).

    The Local Coordinators will constitute the monitoring and drafting committee of the registry.

    The Local Coordinators will be in charge of selecting up to 10 recruiting investigators in each country and will be in charge of the follow up and quality of the recruiting; they will be the link between promoters and recruiting investigators.

    Recruiter Investigators

    The Recruiting Investigators must be gastroenterologists attending an adult population with a gastroenterology outpatient clinic that assists H. pylori infected patients. Before acceptance the outpatient clinic must attend, in a clinical routine basis, patients in which

    1. pylori diagnosis or treatment is indicated. Eradication confirmation tests have to be performed routinely. They will register the study variables of their own routine clinical practice in an e-CRF.

    Study Variables

    Anonymised Patient Identifiers

    • Country/Centre/Investigator

    • Autonumeric Patient identifier number

    • Gender

    • Date of Birth

    • Ethnic Background History and Comorbidity

    • Drug allergies

    • Relevant comorbidities

    • Current concomitant medication Data on Infection

    • Indication for diagnosis and treatment

    • Upper Gastrointestinal tract symptoms

    • Diagnostic Test for current treatment

    • Number and type of previous eradication attempts Prescribed Treatment

    • Drugs

    • Dosage and intakes per day

    • Length of treatment Compliance

    • Adherence to treatment (yes/no >90%) Adverse Events

    • Type of event, intensity, duration and relation with treatment

    • Treatment withdrawal due to adverse events. Efficacy

    • Eradication (yes/no), test used, and date

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    10000 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    European Registry on the Management of Helicobacter Pylori Infection
    Study Start Date :
    Jun 1, 2013
    Anticipated Primary Completion Date :
    Dec 1, 2024
    Anticipated Study Completion Date :
    Dec 1, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Prescribed treatment for H. pylori [1 year]

      Drugs Dosage and intakes Length of treatment

    Secondary Outcome Measures

    1. Adverse Events [1 year]

      Type, intensity, duration and relation with treatment Treatment withdrawal due to adverse event

    2. Efficacy of treatment [1 year]

      Eradication (yes/no), test used and date

    3. Anonymised patient identifiers [1 year]

      Country/Centre/Investigator Autonumeric Patient identifier number Gender Date of Birth Ethnic Background

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Infected adult patients by Helicobacter pylori
    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical University Wien Wien Austria
    2 CHU de Charleroi, Charleroi Charleroi Belgium
    3 Medical University of Sofia Sofia Bulgaria
    4 University Hospital Merkur Zagreb Croatia
    5 Charles University Faculty of Medicine Prague Czechia
    6 Køge University Hospital Køge Denmark
    7 University of Tartu Tartu Estonia
    8 Herttoniemi Hospital, Helsinki Helsinki Finland
    9 Hôpital Pellegrin Bordeaux France
    10 Medizin Uni Magdeburg Magdeburg Germany
    11 Gastroenterology Clinic, Henry Dunant Hospital Athens Greece
    12 Ferencváros Health Centre, Gaastroenterology Budapest Hungary
    13 Adelaide Meath Hospital, Dublin Dublin Ireland
    14 Studio Gasbarrini Roma Italy
    15 Digestive Diseases Centre GASTRO Riga Latvia
    16 Lithuanian university of Health Sciences Hospital Kaunas Lithuania
    17 Ikazia Ziekenhuis/ Erasmus Medisch Centrum Rotterdam Netherlands
    18 Central Hospital of Ostfold Fredrikstad Norway
    19 Departament of Gastroenterology, Medical Centre for Postgraduate Education Warsaw Poland
    20 Porto Porto Portugal
    21 Timisoara Timisoara Romania
    22 Central Scientific Research Institute of Gastroenterology Moscow Russian Federation
    23 Clinical Center of Serbia Belgrade Serbia
    24 DC Rogaska Rogaska Slatina Slovenia
    25 Hospital de La Princesa, Madrid Madrid Spain
    26 Uppsala University Hospital. Uppsala Sweden
    27 University Hospital Basel Basel Switzerland
    28 Dokuz Eylul University School of Medicine Izmir Turkey
    29 National Medical University Kiev Ukraine
    30 Leeds General Infirmiry Hospital Leeds United Kingdom

    Sponsors and Collaborators

    • Javier P. Gisbert

    Investigators

    • Principal Investigator: Javier Pérez Gisbert, MD, Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Javier P. Gisbert, Javier P. Gisbert MD, Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
    ClinicalTrials.gov Identifier:
    NCT02328131
    Other Study ID Numbers:
    • Hp-EuReg
    First Posted:
    Dec 31, 2014
    Last Update Posted:
    Aug 31, 2021
    Last Verified:
    Aug 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 31, 2021