Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33921
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dc.contributor.authorFields, Neville J-
dc.contributor.authorPalmer, Kirsten R-
dc.contributor.authorRolnik, Daniel L-
dc.contributor.authorYo, Jennifer-
dc.contributor.authorNold, Marcel F-
dc.contributor.authorGiles, Michelle L-
dc.contributor.authorKrishnaswamy, Sushena-
dc.contributor.authorSerpa Neto, Ary-
dc.contributor.authorHodges, Ryan J-
dc.contributor.authorMarshall, Sarah A-
dc.date2023-
dc.date.accessioned2023-10-04T02:43:34Z-
dc.date.available2023-10-04T02:43:34Z-
dc.date.issued2023-09-14-
dc.identifier.citationNutrients 2023-09-14; 15(18)en_US
dc.identifier.issn2072-6643-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33921-
dc.description.abstractSince its discovery in late 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been estimated to be responsible for at least 769.3 million infections and over 6.95 million deaths. Despite significant global vaccination efforts, there are limited therapies that are considered safe and effective for use in the management of COVID-19 during pregnancy despite the common knowledge that pregnant patients have a much higher risk of adverse outcomes. A bioactive compound found in broccoli sprout-sulforaphane-is a potent inducer of phase-II detoxification enzymes promoting a series of potentially beneficial effects notably as an antioxidant, anti-inflammatory, and anti-viral. A pilot, double-blinded, placebo-controlled randomised trial is to be conducted in Melbourne, Australia, across both public and private hospital sectors. We will assess a commercially available broccoli sprout extract in pregnant women between 20+0 and 36+0 weeks gestation with SARS-CoV-2 infection to investigate (i) the duration of COVID-19 associated symptoms, (ii) maternal and neonatal outcomes, and (iii) biomarkers of infection and inflammation. We plan to enrol 60 outpatient women with COVID-19 irrespective of vaccination status diagnosed by PCR swab or RAT (rapid antigen test) within five days and randomised to 14 days of oral broccoli sprout extract (42 mg of sulforaphane daily) or identical microcrystalline cellulose placebo. The primary outcome of this pilot trial will be to assess the feasibility of conducting a larger trial investigating the duration (days) of COVID-19-associated symptoms using a broccoli sprout supplement for COVID-19-affected pregnancies. Pregnant patients remain an at-risk group for severe disease following infection with SARS-CoV-2 and currently unclear consequences for the offspring. Therefore, this study will assess feasibility of using a broccoli sprout supplement, whilst providing important safety data for the use of sulforaphane in pregnancy.en_US
dc.language.isoeng-
dc.subjectCOVID-19en_US
dc.subjectSARS-CoV-2en_US
dc.subjectbroccoli sprouten_US
dc.subjectclinical trialen_US
dc.subjectpregnancyen_US
dc.subjectsulforaphaneen_US
dc.titleCO-Sprout-A Pilot Double-Blinded Placebo-Controlled Randomised Trial of Broccoli Sprout Powder Supplementation for Pregnant Women with COVID-19 on the Duration of COVID-19-Associated Symptoms: Study Protocol.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleNutrientsen_US
dc.identifier.affiliationThe Ritchie Centre, Department of Obstetrics and Gynaecology, School of Clinical Sciences, Monash University, Melbourne 3168, Australia.;Monash Health, Monash Medical Centre, Melbourne 3168, Australia.en_US
dc.identifier.affiliationMonash Health, Monash Medical Centre, Melbourne 3168, Australia.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventive Medicine, Melbourne 3004, Australia.;Department of Critical Care, Melbourne Medical School, University of Melbourne, Austin Hospital, Melbourne 3084, Australia.;Department of Intensive Care, Austin Hospital, Melbourne 3084, Australia.;Department of Critical Care Medicine, Hospital Israelita Albert Einstein, Sao Paulo 05652-900, Brazil.en_US
dc.identifier.affiliationMonash Health, Monash Medical Centre, Melbourne 3168, Australia.en_US
dc.identifier.affiliationSchool of Clinical Sciences, Monash University, Melbourne 3168, Australia.en_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.doi10.3390/nu15183980en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-0940-4293en_US
dc.identifier.orcid0000-0001-7421-6291en_US
dc.identifier.orcid0000-0001-9682-4618en_US
dc.identifier.orcid0000-0003-3007-1822en_US
dc.identifier.orcid0000-0001-7276-1405en_US
dc.identifier.pubmedid37764764-
dc.description.volume15-
dc.description.issue18-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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