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Tackling Resistance And HealthCare Economics Through CPE Screening (TRACE-CPE)

16 juni 2026 bijgewerkt door: Imperial College London

Multi-centre Evaluation of Carbapenemase-producing Enterobacterales (CPE) Prevalence and Transmission Dynamics, Recommendations on Screening Strategies, and Health Economics Outcomes Research Impact to Inform Policy Change

The goal of this clinical study is to learn if it is possible to reduce the spread of resistant bacteria called CPEs (Carbapenemase producing Enterobacterales) between patients admitted to hospital.

CPEs can be carried in the gut of people without making them ill. Normally when patients come into hospital, they may undergo a swab test on their bottom to see if CPEs can be grown. This test can take up to 24 hours to produce a result.

The investigators want to use a faster test which takes 2 hours to produce a result, and whether this can make a difference to CPE spread between person to person.

The main questions it aims to answer are:

  1. Why do people carry, transmit or get infected with CPE?
  2. If a faster test was used to look for CPE, would this be better at reducing patient spread in hospital?
  3. Is a faster test also more cost effective?

Participants will:

  1. Be tested by both the usual and faster test when they come into hospital by a swab on their bottom
  2. Where they test positive for CPE they will be asked to answer some questions about their health

Studie Overzicht

Gedetailleerde beschrijving

Carbapenemase-producing Enterobacterales (CPE) are a significant threat to healthcare through their ability to cause drug-resistant infections. These group of bacteria posses enzymes which break down and inactivate carbapenems, a broad spectrum class of antibiotics reserved for severe infections. Transmission of CPEs between patients occur through proximity / contact within their environment in hospital - and is therefore preventable.

Within the individual, initial colonisation with CPE is an important risk factor for development of multi-drug resistant infections which are associated with significant mortality and high hospital costs. The in-hospital transmission of CPE exerts a complex burden across almost all healthcare domains - for example, CPE infection or colonisation renders common surgical antibiotic prophylaxis ineffective, increases morbidity and mortality in vulnerable patient groups such as intensive care, places burdens on the use of single occupancy beds and imposes considerable cost and disruption to care pathways through outbreaks.

Existing microbiological diagnoses of CPEs vary, but commonly involve bacterial culture of a sample such as a rectal swab in laboratory settings followed by phenotypic testing and characterisation of common antibiotic resistant genes (ARGs) through molecular or immunochromatographic approaches, mostly focusing on the "big 5" mechanisms of CPE. Such testing pathways can however be time-consuming, with the median result turnaround time to be between 24-48 hours. Rapid molecular testing for CPE bypasses the bacterial culture step and may allow for robust IPC measures to be implemented in a near real-time fashion including rapid risk stratification of CPE carriage status. Where transmission is suspected, contact tracing using rapid testing early in the transmission cascade could reduce unwanted impact and be cost-effective.

The proposed study examines the utility, cost-benefit in adoption of a rapid based screening approach using rapid CPE testing coupled with an enhanced reporting workflow operating 24 hours a day, compared with existing standard practice. Given the complex interactions of AMR and CPE acquisition and transmission within hospital settings, a comprehensive approach including clinical, epidemiological and health economic costings will be utilised and modelled in order to accurately understand impact. Rapid CPE screening will be incorporated into clinical processes to minimise adverse impact and the research conducted as a pragmatic study.

The rapid test for use in this study is the Cepheid Xpert Carba-R which can detect genes in 5 most prevalent Carbapenemase gene families (including KPC, NDM, VIM, IMP and OXA classes) directly from a rectal swab sample in 50 minutes - this technology is CE-mark approved as an in vitro diagnostic and has undergone NICE technological appraisal

Research hypotheses to be addressed through the study:

  1. The implementation of rapid molecular CPE detection through the Cepheid Xpert Carba-R with an enhanced reporting workflow is associated with greater effectiveness and timeliness in IPC interventions, compared with the existing use of culture-based screening strategies alone. This will lead to reductions in in-hospital transmission of CPE and result in downstream effects for organisation and individuals.
  2. In-hospital screening strategies through rapid molecular CPE testing can be cost-effective from a health economic perspective and acceptable to patient and stakeholders, given particular clinical settings and baseline local CPE prevalence.

This is a multi-centre mixed methods research study consisting of:

  1. A pragmatic prospective interventional interrupted time series study to examine impact of rapid Carbapenemase producing Enterobacterales (CPE) diagnostics and an enhanced reporting workflow in parallel with screening on clinical practice and transmission.
  2. A clinical observational cohort study to characterise individual risk factors for CPE colonisation, epidemiology of colonisation including point-prevalence, and subsequent in-hospital transmission dynamics.
  3. A health economic modelling study utilising hospital and national data to estimate medical costs, patient experience and systems level impact of screening, CPE colonisation and acquisition

The study will take place across two hospital Trusts:

i) Imperial College Healthcare NHS Trust (ICNHT), London ii) Guy's and St Thomas NHS Foundation Trust (GSTT), London

Project 1 will implement the Cepheid Xpert Carba-R rapid test in parallel to routine culture for CPE screening at two hospital sites to understand impact on IPC practice.

Project 2 will capture transmission dynamics, healthcare cost, patient acceptability and quality of life metrics using national datasets, and de-identified healthcare data collected from Project 1. Modelling using health economics outcome research methods will be performed to evaluate CPE screening strategies for a range of scenarios and settings with a view of informing policy. Health economic costings will utilise routinely available clinical data as well as costings metrics and health related grouping code from NHS Hospital Episode Statistics.

Studietype

Ingrijpend

Inschrijving (Geschat)

16000

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

  • Naam: Research Governance and Integrity
  • Telefoonnummer: 020 7594 9832
  • E-mail: RGIT@imperial.ac.uk

Studie Locaties

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • All adult (18 years or older) medical patients admitted to the acute medical unit during the implementation period who undergo routine rectal CPE testing as per local Trust policy and test positive for CPE colonisation through either the rapid test or culture-based methods.

Exclusion Criteria:

  • Patient refusal for rectal screening or
  • Clinical contraindication to rectal swab collection

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Diagnostisch
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Rapid molecular screening
During the study period all eligible patients will undergo the intervention
Participants will undergo a rectal swab and undergo rapid molecular testing for CPE colonisation

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
In-hospital secondary transmission of CPE colonisation
Tijdsspanne: From enrolment to the end of the follow up period at 12 months
The primary outcome measure is the change in secondary in-hospital CPE transmission risk with the introduction of rapid rectal CPE screening. Quantification of transmission risk will be done using transmission dynamics modelling informed by collected clinical and epidemiological data.
From enrolment to the end of the follow up period at 12 months

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Health economic outcomes of CPE colonisation, infection and screening approaches
Tijdsspanne: From enrolment to the end of the follow up period at 12 months
Direct, indirect and opportunity costs associated with CPE colonisation and infection using health economic cost analysis
From enrolment to the end of the follow up period at 12 months
Laboratory measures of diagnostic comparison
Tijdsspanne: From enrolment to the end of the follow up period at 12 months
Concordance metrics between CPE rapid testing and culture including rate, genotype and species.
From enrolment to the end of the follow up period at 12 months
Epidemiological measures of CPE colonisation
Tijdsspanne: From enrolment to the end of the follow up period at 12 months
Patient level risk factors for CPE acquisition, colonisation, and transmission.
From enrolment to the end of the follow up period at 12 months
Qualitative measures including public, stakeholder understanding and acceptability
Tijdsspanne: 24 months
Perspectives on CPE diagnostic implementation, patient and provider acceptability of CPE screening through stakeholder interviews, public engagement and workshops.
24 months
Qualitative study on CPE perspectives through stakeholder interviews, public engagement and focused workshops
Tijdsspanne: 24 months
This will be an adjunctive study with separate approvals process involving interviews with stakeholders to understand views and approaches to the management of CPE and detection. These findings will feed back into the main TRACE-CPE project.
24 months
Point prevalence of CPE
Tijdsspanne: Over the point prevalence period of 1 week
Prevalence of CPE colonisation derived from the number of positive CPE cases divided by the number of individuals undergoing screening.
Over the point prevalence period of 1 week

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Jon Otter, Guy's and St Thomas NHS Trust

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

1 augustus 2026

Primaire voltooiing (Geschat)

1 november 2027

Studie voltooiing (Geschat)

31 maart 2028

Studieregistratiedata

Eerst ingediend

9 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

16 juni 2026

Eerst geplaatst (Werkelijk)

23 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

23 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

16 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual patient data is recorded under the General Data Protection Regulation framework and will not be shared outside the research and clinical teams. Aggregated data will be presented and can be shared under such approvals.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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