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Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/56920
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DC FieldValueLanguage
dc.contributor.authorBlank D.-
dc.coverage.spatialMonash Medical Centre-
dc.date.accessioned2025-12-24T00:55:19Z-
dc.date.available2025-12-24T00:55:19Z-
dc.date.issued2023-09-26-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/56920-
dc.description.abstractWe aim to determine if maternal oxygen supplementation 5-10 min prior to birth of term and near-term infants (32 weeks gestation or above at birth) utilising heated humidified high flow nasal cannula with 100% oxygen at 30-70L/min is feasible at both caesarean section and vaginal births. The information gained from this feasibility study will inform the planned randomised controlled trial of maternal oxygen in very preterm infants.-
dc.titleMaternal OXygen Immediately before birth: The MOXIE feasibility study-
dc.typeClinical trial-
dc.identifier.affiliationPaediatric - Neonatal (Monash Newborn)-
dc.identifier.urlhttps://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=386401-
dc.identifier.externalACTRN12623001037695-
item.openairetypeClinical trial-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptPaediatric - Neonatal (Monash Newborn)-
Appears in Collections:Clinical Trials
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