Collection of Coronavirus COVID-19 Outbreak Samples in New South Wales

  • End date
    Jun 30, 2021
  • participants needed
  • sponsor
    Kirby Institute
Updated on 17 June 2020
Rowena Bull
Primary Contact
Royal North Shore Hospital (4.8 mi away) Contact
+8 other location
coronavirus infection


The objectives of this study are to characterise immune responses in people with CoV-SARS-2 infection and use this knowledge to advance vaccine design, treatment options, and diagnostic reagents. Eligible participants will include people diagnosed with SARS-CoV-2 infection, and may include recently returned travellers and non-travellers in the community presenting to tertiary hospital healthcare facilities. Recruitment will be opportunistic, and sampling intensity may vary depending on the phase of the outbreak. Participants can be enrolled at any timepoint (up to 6 months) following diagnosis of SARS-CoV-2 infection (COVID-19). Blood samples and clinical data will be collected.

Treatment Biological sample and clinical data collection
Clinical Study IdentifierNCT04383652
SponsorKirby Institute
Last Modified on17 June 2020

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Inclusion Criteria

Gender: Male or Female
Do you have any of these conditions: Pathogen Infection Covid-19 Infection or *COVID-19 Infection or SARS-CoV-2 (COVID-19) Infection or Severe Coronavirus Disease (COVID-19) or Covid-19 o...?
Main cohort
Diagnosed with CoV-SARS-2 infection
16 years of age or older
Have provided informed consent Paediatric cohort
Diagnosed with CoV-SARS-2 infection
Less than 16 years of age
Informed consent provided by parent or caregiver

Exclusion Criteria

Main cohort
15 years of age or younger
Inability or unwillingness to provide informed consent or abide by the requirements of the study Paediatric cohort
16 years of age or older
Inability or unwillingness of parent or caregiver to provide informed consent or abide by the requirements of the study -
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Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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Step 3 Enroll in the clinical study

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Step 4 Get your study results

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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