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E. Coli InfectionEXPECT-2NCT04117113

Study to Collect Information About Invasive Disease Caused by Extraintestinal Pathogenic Escherichia Coli-2 (EXPECT-2)

An observational study of E. Coli Infection, run by UMC Utrecht at 8 sites in 8 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to collect information from study participants who are hospitalized with an invasive disease caused by Extraintestinal pathogenic E. coli (ExPEC). This information will be used to support the development of a new vaccine to prevent Extraintestinal pathogenic Escherichia coli (ExPEC). E. Read more about this study

Who is it for?
Ages 60 years and older
Conditions the study is for
E. Coli Infection
How many people
238 participants
Where
8 sitesin 8 countries
Study dates
22 Oct 2019to 12 May 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients hospitalized and having culture-confirmed IED.

Who may be able to join

  • Patients aged 60 years or older and hospitalized for IED at the start of the study.
  • Culture confirmation of E. coli (1) in normally sterile body sites including blood, and/or (2) in urine in the presence of clinical criteria of an invasive infection (raise in SOFA score >1, sepsis, or septic shock consequent to the infection).
  • For those countries and/or study sites where no waiver for informed consent/assent has been obtained prior to data collection, eligible patients must sign a participation agreement/ICF/IAF allowing data collection and source data verification in accordance with local requirements and/or sponsor policy. For deceased patients, a participation agreement/ICF/IAF must be signed by the patient's next of kin.

Who cannot join

  • There are no exclusion criteria for this study.

Trial locations and contacts

8 sites in 8 countries.

8 sites in 8 countries

United States1 site
  • Duke Clinical Research Institute

    Durham, North Carolina, 27701

Other trials in United States

Canada1 site
  • Duke Clinical Research Institute

    Greater Sudbury

Other trials in Canada

France1 site
  • CHU Limoges - CIC

    Limoges, 87042

Other trials in France

Germany1 site
  • UKK Uniclinic Cologne

    Cologne, 50937

Other trials in Germany

Italy1 site
  • University of Verona

    Verona

Other trials in Italy

Japan1 site
  • Janssen Pharmaceutical K.K.

    Tokyo, Chiyoda-ku

Other trials in Japan

Spain1 site
  • Andalusian Public Foundation for Health Research Management in Seville (FISEVI)

    Seville, 41013

Other trials in Spain

United Kingdom1 site
  • University of Oxford

    Oxford, OX1 2JD

Other trials in United Kingdom

About this study

Official title: Prospective Epidemiological Study to Estimate the O-serotype Distribution of Extraintestinal Pathogenic Escherichia Coli (ExPEC) Isolated From Hospitalized Patients Aged 60 Years or Older With Invasive ExPEC Disease (IED) and to Evaluate the Clinical Case Definition and Risk Factors.

The purpose of this study is to collect information from study participants who are hospitalized with an invasive disease caused by Extraintestinal pathogenic E. coli (ExPEC). This information will be used to support the development of a new vaccine to prevent Extraintestinal pathogenic Escherichia coli (ExPEC). E. coli bacteria are a leading cause of serious infections. Especially adults older than 60 years have a higher risk of developing such infections. To date, there is no vaccine available to prevent E. coli infections. To support the development of a vaccine, more information about E. coli infections is first needed. This information will be collected in the current study, such as:

  • Medical information such as medical history, diagnosis, duration of hospitalization
  • Treatment and outcome of the Extraintestinal pathogenic Escherichia coli (ExPEC)
  • Laboratory information
Read the detailed description

Janssen Research \& Development is developing ExPEC10V, a 10-valent conjugate vaccine comprising the 10 most predominant O-polysaccharides of ExPEC.

Invasive ExPEC Disease (IED) is defined as an acute illness consistent with bacterial infection that is microbiologically confirmed either by the isolation and identification of E. coli from blood or other normally sterile body sites, or by the isolation and identification of E. coli from urine in a patient with signs and symptoms of invasive disease (presence of systemic inflammatory response syndrome [SIRS], sepsis or septic shock) and no other identifiable source of infection.

ExPEC is the most common cause of infection in humans resulting from gram-negative bacteria. ExPEC comprises a pathogenic group of E. coli strains, possessing the ability to colonize and infect normally sterile body sites and to cause Invasive ExPEC Disease (IED).

ExPEC causes the vast majority of urinary tract infections (UTIs), is the second most frequent cause of neonatal bacteremia and meningitis, and is a leading cause of adult IED, in particular bacteremia and sepsis.

Although IED affects all age categories, adults aged 60 years or older have an increased risk of developing IED, including bacteremia and sepsis. The incidence of community-acquired ExPEC bacteremia increases with age, occurring at a rate of 150/100,000 person-years in the United States (US) adults aged 65 years and older, and 452/100,000 person-years in adults aged 85 years and older. Similar trends have been observed in Europe. In the US, it is estimated that up to 40,000 patients die annually due to IED, in particular from E. coli sepsis. Overall case-fatality rates for ExPEC bacteremia range from 13% to 19% but may be much higher (up to 60%) in the elderly with healthcare-associated infections.

The increase in multidrug resistance (ie, resistance to two or more antibiotic classes) among ExPEC strains, such as E. coli sequence type 131:O25B, represents a major challenge for prevention and management of ExPEC infections. Global morbidity, hospitalization and mortality rates due to ExPEC infections are substantial and increasing due to aging populations and increasing prevalence of antibiotic resistant ExPEC strains, and associated with increasing healthcare costs in both Europe and the US.

This hospital-based prospective epidemiological study will assess the O-serotype and O-genotype distribution in E. coli isolates causing IED overall and by subgroup based on risk factors. Detailed demographic and clinical data, including information on hospital routes, from patients with IED will be collected in this study to further characterize the clinical setting in this patient population. This study will also provide data to compare the clinical criteria of IED used by the study site with the proposed Phase 3 clinical case definition for IED in adults aged 60 years or older for future clinical studies in this patient population. No study drug will be administered in this non interventional study.

Medical subject headings
Escherichia coli Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT04117113
Study groupRoleWhat they receive
Elderly, 60+ hospitalized with Invasive ExPEC DiseasePatients 60 years or older hospitalized with Invasive Extraintestinal Pathogenic Escherichia coli Disease.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Distribution of E. coli O-serotypes causing IED in adults aged 60 years or older, as percentage of the total study population.

    Measured: 12 months

  2. Distribution of E. coli O-genotypes causing IED in adults aged 60 years or older, as percentage of the total study population.

    Measured: 12 months

  3. Distribution of IED in adults aged 60 years or older over the following clinical case definitions: "Pyelonephritis", "Urosepsis", "Meningitis", "Arthritis", "Sepsis of unknown origin" and "Others", as a percentage of the total study population.

    Measured: 12 months

Secondary outcomes (8)
  1. Proportion of non-bacteremic and bacteremic IED of the total number of IED cases.

    Measured: 12 months

  2. Listing of IED patients with specific risk factors for IED as a proportion of all IED patients.

    Specific risk factors for IED are medical conditions (e.g. kidney disease, history of urinary tract infection in prior 12 months), sociodemographic characteristics (e.g. age, gender) and medication use (e.g. immunosuppressive medication)

    Measured: 12 months

  3. Type of infection (community acquired, hospital-acquired or healthcare-associated) .

    Measured: 12 months

  4. Source of infection (presence of an infectious focus within 30 days prior to IED).

    Measured: 12 months

  5. Susceptibility of the cultured E. coli strains to antibiotics as determined by EUCAST standards (version9.0) to β-lactam antibiotics.

    Measured: 12 months

  6. O-antigen expression profiles

    Measured: 12 months

  7. Mortality associated with IED

    Measured: 12 months

  8. Department where patient is presented/admitted to the hospital (emergency ward, general ward, intensive care unit)

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Oct 2019
  2. Study start22 Oct 2019
  3. Primary completion31 Jan 2021
  4. Study completion12 May 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
238 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04117113
Sponsor's protocol ID
VAC52416BAC0006
Acronym
EXPECT-2
Status last verified
Sep 2021
First submitted
22 May 2019
Last updated
21 Sep 2021
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of E. Coli Infection, run by UMC Utrecht at 8 sites in 8 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 21 Sep 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites in United States, Canada, France, Germany, Italy and 3 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Distribution of E. coli O-serotypes causing IED in adults aged 60 years or older, as percentage of the total study population. (time frame: 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Sep 2021.

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