Development of a portable point-of-care device for rapid testing of SARS-CoV-2 [Added supplement: COVID-19 Variant Supplement]
- Funded by Canadian Institutes of Health Research (CIHR)
- Total publications:0 publications
Grant number: 170630, 175533
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Key facts
Disease
COVID-19Start & end year
20202022Known Financial Commitments (USD)
$739,500Funder
Canadian Institutes of Health Research (CIHR)Principal Investigator
Denis BoudreauResearch Location
CanadaLead Research Institution
Université LavalResearch 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 novel coronavirus (SARS-CoV-2) outbreak that started in December 2019 triggered unprecedented measures to avoid a global pandemic. However, China has been particularly hit with over 70 000 confirmed cases, of which about 80% are in Hubei province. Wuhan, capital city of Hubei, is considered ground zero of the outbreak. Testing is typically performed at centralized facilities with highly qualified personnel operating specialized equipment, RT-qPCR being the current method of choice and DNA sequencing a second choice. The response time between sampling patients and obtaining clinically relevant information usually depends on sample shipping time and clinical lab capacity. In this current outbreak containment situation in China, large portions of the population are quarantined, travel is restricted, and clinical labs are operating well over capacity. We propose to develop a rapid point-of-care test to help mitigate the outbreak of COVID-19. The RNA-based test will be performed with a high sensitivity, label-free sensing method. RNA purification and amplification will not be required. The instrumentation needed will be portable and lightweight to enable frontline workers to rapidly test for SARS-CoV-2. The assay will be developed with an easy-to-use platform that can be operated by untrained personnel. It can thereby be deployed locally, within regions of quarantine at a temporary health centers and neighbourhood clinics, reducing flow of people in urban centers; it can be shipped and used in remote or isolated areas including cruise ships