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dc.contributor.authorJardine, Meg
dc.date.accessioned2024-02-22T21:58:18Z
dc.date.available2024-02-22T21:58:18Z
dc.date.issued2024-02-23
dc.identifier.urihttps://hdl.handle.net/2123/32242
dc.description.abstractThis dataset includes up to 787 participants receiving an oral angiotensin receptor blocker (no placebo per standard of care in Australia, and telmisartan in India) recruited from seventeen hospitals in India and Australia. Baseline data includes demographics (age, sex, ethnicity, height, and weight), pregnancy status, smoking status, and co-morbidities. Primary follow-up data was collected daily from days 1 to 28 during treatment period and will include clinical outcome (Clinical Health Score), temperature, respiratory measures (oxygen saturation, use of supplemental oxygen), hypotension (vasopressor requirement), incidence of acute kidney injury, and hyperkalaemia (serum potassium concentration of >6.0 mmol/L).en_AU
dc.rightsOtheren_AU
dc.titleControlled evaLuation of Angiotensin Receptor Blockers for COVID-19 respIraTorY Disease (CLARITY) dataseten_AU
dc.typeDataseten_AU
dc.identifier.doi10.25910/ghrw-5k88
dc.rights.otherAccess can be requested via the Health Data Australia catalogue (https://researchdata.edu.au/health). A copy of the Data Sharing Guidelines can be found in https://rb.gy/bgrcq. For further information please contact the Health Studies Australian National Data Asset (HeSANDA) SHP-CTC node ([email protected]).en_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::NHMRC Clinical Trials Centreen_AU
workflow.metadata.onlyYesen_AU


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