A randomised open-label trial to assess outpatient induction of labour (HOMEIND) and compare efficacy of Propess vs Dilapan-S® for induction of labour at 39 weeks’ gestation in normal risk nulliparous women: study protocol for a randomised controlled trial

BACKGROUND: Induction of labour (IOL) at 39 weeks has been shown to decrease maternal and neonatal adverse outcomes. Given the growing demand for 39-week IOL, it is imperative that effective methods be assessed for induction in the outpatient setting. The aim of this study is to answer the clinical...

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Detalles Bibliográficos
Autores principales: Nicholson, Sarah M., Smith, Orla, Hatt, Susan, Molphy, Zara, Dicker, Patrick, Flood, Karen, Malone, Fergal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946860/
https://www.ncbi.nlm.nih.gov/pubmed/36814336
http://dx.doi.org/10.1186/s13063-023-07174-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946860/
https://www.ncbi.nlm.nih.gov/pubmed/36814336
http://dx.doi.org/10.1186/s13063-023-07174-7

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