Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25425
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dc.contributor.authorPerera, Marlon-
dc.contributor.authorEl Khoury, John-
dc.contributor.authorChinni, Vidyasagar-
dc.contributor.authorBolton, Damien M-
dc.contributor.authorQu, Liang G-
dc.contributor.authorJohnson, Paul D R-
dc.contributor.authorTrubiano, Jason-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorJones, Daryl A-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorPatel, Oneel-
dc.contributor.authorIschia, Joseph J-
dc.date2020-12-02-
dc.date.accessioned2020-12-06T21:53:54Z-
dc.date.available2020-12-06T21:53:54Z-
dc.date.issued2020-12-02-
dc.identifier.citationBMJ open 2020; 10(12): e040580en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25425-
dc.description.abstractSARS-CoV-2 (COVID-19) has caused an international pandemic of respiratory illness, resulting in significant healthcare and economic turmoil. To date, no robust vaccine or treatment has been identified. Elemental zinc has previously been demonstrated to have beneficial effects on coronaviruses and other viral respiratory infections due to its effect on RNA polymerase. Additionally, zinc has well-demonstrated protective effects against hypoxic injury-a clear mechanism of end-organ injury in respiratory distress syndrome. We aimed to assess the effect of high-dose intravenous zinc (HDIVZn) on SARS-CoV-2 infection. The end of study analyses will evaluate the reduction of impact of oxygen saturations or requirement of oxygen supplementation. We designed a double-blind randomised controlled trial of daily HDIVZn (0.5 mg/kg) versus placebo. Primary outcome measures are lowest oxygen saturation (or greatest level of supplemental oxygenation) for non-ventilated patients and worst PaO2/FiO2 for ventilated patients. Following power calculations, 60 hospitalised patients and 100 ventilated patients will be recruited to demonstrate a 20% difference. The duration of follow-up is up to the point of discharge. Ethical approval was obtained through the independent Human Research Ethics Committee. Participant recruitment will commence in May 2020. Results will be published in peer-reviewed medical journals. ACTRN126200000454976.en
dc.language.isoeng-
dc.subjectinfectious diseasesen
dc.subjectpublic healthen
dc.subjectrespiratory infectionsen
dc.subjectvirologyen
dc.subjectCOVID-19en
dc.titleRandomised controlled trial for high-dose intravenous zinc as adjunctive therapy in SARS-CoV-2 (COVID-19) positive critically ill patients: trial protocol.en
dc.typeJournal Articleen
dc.identifier.journaltitleBMJ openen
dc.identifier.affiliationSurgeryen
dc.identifier.affiliationInfectious Diseasesen
dc.identifier.affiliationRespiratory and Sleep Medicineen
dc.identifier.affiliationIntensive Careen
dc.identifier.affiliationGeneral Medicineen
dc.identifier.doi10.1136/bmjopen-2020-040580en
dc.type.contentTexten
dc.identifier.orcid0000-0002-1138-6389en
dc.identifier.orcid0000-0002-5111-6367en
dc.identifier.pubmedid33268419-
local.name.researcherBellomo, Rinaldo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
crisitem.author.deptSurgery-
crisitem.author.deptUrology-
crisitem.author.deptSurgery-
crisitem.author.deptSurgery-
crisitem.author.deptUrology-
crisitem.author.deptUrology-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCentre for Antibiotic Allergy and Research-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptUrology-
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