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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04383652
Acronym
COSiN
Enrollment
200
Registered
2020-05-12
Start date
2020-05-06
Completion date
2022-06-30
Last updated
2021-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID

Brief 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.

Interventions

OTHERBiological sample and clinical data collection

Plasma and serum will be collected at day 0, day 7, day 14, 1 month and 4 months post diagnosis. Clinical data related to COVID-19 diagnosis, symptoms, and outcomes will be collected.

Sponsors

Kirby Institute
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Main cohort 1. Diagnosed with CoV-SARS-2 infection 2. 16 years of age or older 3. Have provided informed consent Paediatric cohort <!-- --> 1. Diagnosed with CoV-SARS-2 infection 2. Less than 16 years of age 3. Informed consent provided by parent or caregiver

Exclusion criteria

Main cohort <!-- --> 1. 15 years of age or younger 2. Inability or unwillingness to provide informed consent or abide by the requirements of the study Paediatric cohort <!-- --> 1. 16 years of age or older 2. Inability or unwillingness of parent or caregiver to provide informed consent or abide by the requirements of the study -

Design outcomes

Primary

MeasureTime frameDescription
Coronavirus sequencing4 months post COVID-19 diagnosis.The viruses will be sequenced to to help understand epitope specificity

Secondary

MeasureTime frameDescription
Coronavirus culturing4 months post COVID-19 diagnosis.The viruses will then be either cultured to study the immune response against them in culture.

Countries

Australia

Contacts

Primary ContactRowena Bull
r.bull@unsw.edu.au0293850900
Backup ContactMarianne Martinello
mmartinello@Kirby.unsw.edu.au0293850900

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026