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

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    Kirby Institute
Updated on 19 February 2024
covid-19
SARS
coronavirus infection
acute respiratory syndrome (sars)

Summary

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.

Details
Condition COVID
Age 100years or below
Treatment Biological sample and clinical data collection
Clinical Study IdentifierNCT04383652
SponsorKirby Institute
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

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 -
Clear my responses

How to participate?

Step 1 Connect with a study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

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

Learn more

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.

Learn more

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

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.