COVID-19 National DiagnOstic Research and Evaluation Platform (CONDOR)

  • Funded by Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR)
  • Total publications:11 publications

Grant number: COV0051

Grant search

Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2022
  • Known Financial Commitments (USD)

    $1,766,611.88
  • Funder

    Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR)
  • Principal Investigator

    N/A

  • Research Location

    United Kingdom
  • Lead Research Institution

    Manchester University NHS Foundation Trust
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

The international demand for accurate diagnostics to improve patient health and optimise healthcare resources in the COVID-19 (SARS-CoV-2) pandemic is steadily increasing. In response to the pandemic, the life sciences industry has seen an influx of new in vitro diagnostic tests (IVDs). However, recent evaluations of these diagnostics are mainly single centred, employ differing reference standards with variable protocols which means limited comparability between tests and ultimately a longer time to useful results to guide clinical care. Leveraging our existing infrastructure and collective expertise, we propose to work as a collaborative national platform for COVID-19 diagnostics research and evaluation. To ensure a methodologically robust, standardised approach to the evaluation process and to avoid duplication of effort, we will mobilise a network of hospital laboratories, primary and secondary care settings and care homes. CONDOR will deliver rapid, robust evaluation of medical tests to support diagnosis and management of patients with suspected COVID-19. This collaborative platform will also place the UK in a unique position to rapidly evaluate and adopt novel diagnostics into clinical practice when faced with future pandemics. The platform has 4 elements: 1) A central triage point for novel diagnostics through an expert steering committee 2) Analytical performance evaluation of IVDs (molecular, antigen and antibody tests) via a laboratory network 3) Evaluation of clinical performance (diagnostic accuracy) of IVDs (self-tests, POCTs and laboratory platforms) in established clinical networks 4) Cross cutting workstreams. a. Care pathway analysis for COVID-19 diagnostics b. Evaluating utility and usability in laboratory and clinical settings

Publicationslinked via Europe PMC

Last Updated:41 minutes ago

View all publications at Europe PMC

Evaluation of the diagnostic accuracy of two point-of-care tests for COVID-19 when used in symptomatic patients in community settings in the UK primary care COVID diagnostic accuracy platform trial (RAPTOR-C19).

Multicenter Diagnostic Evaluation of OnSite COVID-19 Rapid Test (CTK Biotech) among Symptomatic Individuals in Brazil and the United Kingdom.

Diagnostic performance of GENEDIA W and ActiveXpress+ COVID-19 antigens tests among symptomatic individuals in Peru and The United Kingdom.

Perceived feasibility, facilitators and barriers to incorporating point-of-care testing for SARS-CoV-2 into emergency medical services by ambulance service staff: a survey-based approach.

COVID-19 rapid diagnostics: practice review.

Strategies to implement SARS-CoV-2 point-of-care testing into primary care settings: a qualitative secondary analysis guided by the Behaviour Change Wheel.

Care pathway and prioritization of rapid testing for COVID-19 in UK hospitals: a qualitative evaluation.

COVID-19 point-of-care testing in care homes: what are the lessons for policy and practice?

COVID-19: Rapid antigen detection for SARS-CoV-2 by lateral flow assay: A national systematic evaluation of sensitivity and specificity for mass-testing.