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dc.contributor.authorDenholm, Justin T.en
dc.contributor.authorDavis, Joshuaen
dc.contributor.authorPaterson, Daviden
dc.contributor.authorRoberts, Jasonen
dc.contributor.authorMorpeth, Susanen
dc.contributor.authorSnelling, Thomasen
dc.contributor.authorZentner, Dominicaen
dc.contributor.authorRees, Meganen
dc.contributor.authorO'Sullivan, Matthewen
dc.contributor.authorPrice, Daviden
dc.contributor.authorBowen, Ashaen
dc.contributor.authorTong, Steven Y. C.en
dc.date.accessioned2020-08-14
dc.date.available2020-08-14
dc.date.issued2020en
dc.identifier.urihttps://hdl.handle.net/2123/23040
dc.description.abstractObjectives: 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.isoenen
dc.rightsOther
dc.subjectCOVID-19en
dc.subjectCoronavirusen
dc.titleThe 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 trialen
dc.typeArticleen
dc.identifier.doi10.1186/s13063-020-04576-9
dc.relation.otherHealth Research Council of New Zealanden
usyd.facultyFaculty of Medicine and Health, Sydney Medical Schoolen


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