The Australasian COVID-19 Trial (ASCOT) to assess clinical outcomes in hospitalised patients with SARS-CoV-2 infection (COVID-19) treated with lopinavir/ritonavir and/or hydroxychloroquine compared to standard of care: A structured summary of a study protocol for a randomised controlled trial
| Field | Value | Language |
| dc.contributor.author | Denholm, Justin T. | en |
| dc.contributor.author | Davis, Joshua | en |
| dc.contributor.author | Paterson, David | en |
| dc.contributor.author | Roberts, Jason | en |
| dc.contributor.author | Morpeth, Susan | en |
| dc.contributor.author | Snelling, Thomas | en |
| dc.contributor.author | Zentner, Dominica | en |
| dc.contributor.author | Rees, Megan | en |
| dc.contributor.author | O'Sullivan, Matthew | en |
| dc.contributor.author | Price, David | en |
| dc.contributor.author | Bowen, Asha | en |
| dc.contributor.author | Tong, Steven Y. C. | en |
| dc.date.accessioned | 2020-08-14 | |
| dc.date.available | 2020-08-14 | |
| dc.date.issued | 2020 | en |
| dc.identifier.uri | https://hdl.handle.net/2123/23040 | |
| dc.description.abstract | Objectives: To determine if lopinavir/ritonavir +/- hydroxychloroquine will reduce the proportion of participants who survive without requiring ventilatory support, 15 days after enrolment, in adult participants with non-critically ill SARS-CoV-2 infection. | en |
| dc.language.iso | en | en |
| dc.rights | Other | |
| dc.subject | COVID-19 | en |
| dc.subject | Coronavirus | en |
| dc.title | The Australasian COVID-19 Trial (ASCOT) to assess clinical outcomes in hospitalised patients with SARS-CoV-2 infection (COVID-19) treated with lopinavir/ritonavir and/or hydroxychloroquine compared to standard of care: A structured summary of a study protocol for a randomised controlled trial | en |
| dc.type | Article | en |
| dc.identifier.doi | 10.1186/s13063-020-04576-9 | |
| dc.relation.other | Health Research Council of New Zealand | en |
| usyd.faculty | Faculty of Medicine and Health, Sydney Medical School | en |
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