Data

The MyTIME clinical trial

The University of Western Australia
Bradfield, Zoe ; White, Scott ; Sharp, Mary ; Keelan, Jeff ; Rose, Monique ; Warland, Jane ; Kuliukas, Lesley ; Davies-Tuck, Miranda ; Callander, Emily ; Ekin, Kylie ; Ladyman, Clare ; Doherty, Dorota
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.60854/4rqm-n332&rft.title=The MyTIME clinical trial&rft.identifier=10.60854/4rqm-n332&rft.publisher=Curtin University&rft.description=HeSANDA 1.0.0 To study is a double-blind, randomised, placebo-controlled trial of daily oral melatonin administration from 39 weeks' gestation in nulliparous pregnant women to reduce induction of labour rates. Induction of labour will be the primary endpoint of the study.&rft.creator=Bradfield, Zoe &rft.creator=White, Scott &rft.creator=Sharp, Mary &rft.creator=Keelan, Jeff &rft.creator=Rose, Monique &rft.creator=Warland, Jane &rft.creator=Kuliukas, Lesley &rft.creator=Davies-Tuck, Miranda &rft.creator=Callander, Emily &rft.creator=Ekin, Kylie &rft.creator=Ladyman, Clare &rft.creator=Doherty, Dorota &rft.date=2024&rft.coverage=Australia&rft_subject=FOS:Medical and health sciences&rft.type=dataset&rft.language=English Access the data

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HeSANDA 1.0.0
To study is a double-blind, randomised, placebo-controlled trial of daily oral melatonin administration from 39 weeks' gestation in nulliparous pregnant women to reduce induction of labour rates. Induction of labour will be the primary endpoint of the study.

Notes

External Organisations
Curtin University; University of Adelaide; Monash University; University of Technology Sydney
Associated Persons
Monique Rose (Contributor); Jane Warland (Contributor); Lesley Kuliukas (Contributor); Miranda Davies-Tuck (Contributor); Emily Callander (Contributor); Kylie Ekin (Contributor); Clare Ladyman (Contributor)

Issued: 2024

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Spatial Coverage And Location

text: Australia

Subjects

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