Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34411
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dc.contributor.authorYoung, Paul J-
dc.contributor.authorArabi, Yaseen M-
dc.contributor.authorBagshaw, Sean M-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorFujii, Tomoko-
dc.contributor.authorHaniffa, Rashan-
dc.contributor.authorHodgson, Carol L-
dc.contributor.authorVijayaraghavan, Bharath Kumar Tirupakuzhi-
dc.contributor.authorLitton, Edward-
dc.contributor.authorMackle, Diane-
dc.contributor.authorNichol, Alistair D-
dc.contributor.authorKasza, Jessica-
dc.date2023-
dc.date.accessioned2023-12-13T05:24:44Z-
dc.date.available2023-12-13T05:24:44Z-
dc.date.issued2022-06-06-
dc.identifier.citationCritical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine 2022-06-06; 24(2)en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34411-
dc.description.abstractBackground: The effect of conservative versus liberal oxygen therapy on 90-day in-hospital mortality in patients who require unplanned invasive mechanical ventilation in an intensive care unit (ICU) is uncertain and will be evaluated in the mega randomised registry trial research program (Mega-ROX). Objective: To summarise the protocol and statistical analysis plan for Mega-ROX. Design, setting and participants: Mega-ROX is a 40 000-patient parallel-group, registry-embedded clinical trial in which adults who require unplanned invasive mechanical ventilation in an ICU will be randomly assigned to conservative or liberal oxygen therapy. Within this overarching trial research program, three nested parallel randomised controlled trials will be conducted. These will include patients with suspected hypoxic ischaemic encephalopathy (HIE) following resuscitation from a cardiac arrest, patients with sepsis, and patients with non-HIE acute brain injuries or conditions. Main outcome measures: The primary outcome is in-hospital allcause mortality up to 90 days from the date of randomisation. Secondary outcomes include duration of survival, duration of mechanical ventilation, ICU length of stay, hospital length of stay, and proportion of patients discharged home. Results and conclusions: Mega-ROX will compare the effect of conservative versus liberal oxygen therapy on 90-day in-hospital mortality in critically ill adults who receive unplanned invasive mechanical ventilation in an ICU. The protocol and a pre-specified approach to analyses are reported here to mitigate analysis bias. Trial registration: Australian and New Zealand Clinical Trials Registry (ANZCTRN 12620000391976).en_US
dc.language.isoeng-
dc.titleProtocol and statistical analysis plan for the mega randomised registry trial research program comparing conservative versus liberal oxygenation targets in adults receiving unplanned invasive mechanical ventilation in the ICU (Mega-ROX).en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCritical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicineen_US
dc.identifier.affiliationIntensive Care Unit, Wellington Hospital, Wellington, New Zealand.;Medical Research Institute of New Zealand, Wellington, New Zealand.;Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.;Department of Critical Care, University of Melbourne, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationCollege of Medicine, King Saud Bin Abdulaziz University for Health Sciences, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.;Intensive Care Department, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, University of Alberta and Alberta Health Services, Edmonton, Alberta, Canada.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.;Department of Critical Care, University of Melbourne, Melbourne, VIC, Australia.;Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia.;Department of Intensive Care, Royal Melbourne Hospital, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.;Intensive Care Unit, Jikei University Hospital, Tokyo, Japan.;Department of Health Promotion and Human Behavior, School of Public Health, Kyoto University, Kyoto, Japan.en_US
dc.identifier.affiliationNuffield Department of Medicine, University of Oxford, Oxford, UK.;National Intensive Care Surveillance, Mahidol-Oxford Tropical Medicine Research Unit (NICS-MORU), Colombo, Sri Lanka.;University College Hospital, London, UK.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.;Department of Critical Care, University of Melbourne, Melbourne, VIC, Australia.;Intensive Care Unit, Alfred Health, Melbourne, VIC, Australia.;George Institute for Global Health, Sydney, NSW, Australia.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, Apollo Hospitals, Chennai, Tamil Nadu, India.;George Institute for Global Health, New Delhi, Delhi, India.en_US
dc.identifier.affiliationIntensive Care Unit, Fiona Stanley Hospital, Perth, WA, Australia.;Medical School, University of Western Australia, Perth, WA, Australia.en_US
dc.identifier.affiliationMedical Research Institute of New Zealand, Wellington, New Zealand.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.;Intensive Care Unit, Alfred Health, Melbourne, VIC, Australia.;School of Medicine, University College Dublin, Dublin, Ireland.;Department of Anaesthesia, Intensive Care and Pain Medicine, St Vincent's University Hospital, Dublin, Ireland.en_US
dc.identifier.affiliationSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.doi10.51893/2022.2.OA4en_US
dc.type.contentTexten_US
dc.identifier.pubmedid38045600-
dc.description.volume24-
dc.description.issue2-
dc.description.startpage137-
dc.description.endpage149-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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