Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20329
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dc.contributor.authorCabrini, Luca-
dc.contributor.authorBrusasco, Claudia-
dc.contributor.authorRoasio, Agostino-
dc.contributor.authorCorradi, Francesco-
dc.contributor.authorNardelli, Pasquale-
dc.contributor.authorFilippini, Matteo-
dc.contributor.authorCotticelli, Virginia-
dc.contributor.authorBelletti, Alessandro-
dc.contributor.authorFerrara, Lorenzo-
dc.contributor.authorAntonucci, Elio-
dc.contributor.authorBaiardo Redaelli, Martina-
dc.contributor.authorLattuada, Marco-
dc.contributor.authorColombo, Sergio-
dc.contributor.authorOlper, Luigi-
dc.contributor.authorPonzetta, Giuseppe-
dc.contributor.authorAnaniadou, Sofia-
dc.contributor.authorMonti, Giacomo-
dc.contributor.authorSeveri, Luca-
dc.contributor.authorMaj, Giulia-
dc.contributor.authorGiardina, Giuseppe-
dc.contributor.authorBiondi-Zoccai, Giuseppe-
dc.contributor.authorBenedetto, Umberto-
dc.contributor.authorGemma, Marco-
dc.contributor.authorCavallero, Sarah Sophia Michelle-
dc.contributor.authorHajjar, Ludhmila Abrahao-
dc.contributor.authorZangrillo, Alberto-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorLandoni, Giovanni-
dc.date2019-02-07-
dc.date.accessioned2019-03-04T22:04:17Z-
dc.date.available2019-03-04T22:04:17Z-
dc.date.issued2019-03-
dc.identifier.citationContemporary clinical trials 2019; 78: 126-132-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20329-
dc.description.abstractFew randomized trials have evaluated the use of non-invasive ventilation (NIV) for early acute respiratory failure (ARF) in non-intensive care unit (ICU) wards. The aim of this study is to test the hypothesis that early NIV for mild-moderate ARF in non-ICU wards can prevent development of severe ARF. Pragmatic, parallel group, randomized, controlled, multicenter trial. Non-intensive care wards of tertiary centers. Non-ICU ward patients with mild to moderate ARF without an established indication for NIV. Patients will be randomized to receive or not receive NIV in addition to best available care. We will enroll 520 patients, 260 in each group. The primary endpoint of the study will be the development of severe ARF. Secondary endpoints will be 28-day mortality, length of hospital stay, safety of NIV in non-ICU environments, and a composite endpoint of all in-hospital respiratory complications. This trial will help determine whether the early use of NIV in non-ICU wards can prevent progression from mild-moderate ARF to severe ARF.-
dc.language.isoeng-
dc.subjectARF-
dc.subjectAcute respiratory failure-
dc.subjectNIV-
dc.subjectNon-invasive ventilation-
dc.titleNon-invAsive VentIlation for early General wArd respiraTory failurE (NAVIGATE): A multicenter randomized controlled study. Protocol and statistical analysis plan.-
dc.typeJournal Article-
dc.identifier.journaltitleContemporary clinical trials-
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italy-
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care, EO Ospedali Galliera, Genova, Italy-
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care, Ospedale Civile di Asti, Asti, Italy-
dc.identifier.affiliationUniversità degli Studi di Pisa, Pisa, Italy-
dc.identifier.affiliationDepartment of Anesthesia and Critical Care Medicine, Spedali Civili, Brescia, Italy-
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care, Aurelia Hospital, Roma, Italy-
dc.identifier.affiliationDepartment of Pneumology, Ospedale Villa Scassi ASL 3 Genovese, Genova, Italy-
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care, Azienda Ospedaliera San Camillo Forlanini, Roma, Italy-
dc.identifier.affiliationBristol Heart Institute, University of Bristol, School of Clinical Sciences, Bristol, United Kingdom-
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care, Ospedale Civile di Asti, Asti, Italy-
dc.identifier.affiliationDepartment of Cardiopneumology, Heart Institute, Faculty of Medicine, University of Sao Paulo, Hospital Siriolibanes, Sao Paulo, Brazil-
dc.identifier.affiliationIRCCS NEUROMED, Pozzilli, IS, Italy-
dc.identifier.affiliationDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italyen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Center, Monash University, Melbourne, VIC, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationVita-Salute San Raffaele University Milan, Italyen
dc.identifier.doi10.1016/j.cct.2019.02.001-
dc.identifier.orcid0000-0002-1650-8939-
dc.identifier.pubmedid30739002-
dc.type.austinJournal Article-
local.name.researcherBellomo, Rinaldo
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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