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Feasibility of Conducting a Trial Assessing Benefits and Risks of Planned Caesarean Section Versus Planned Vaginal Birth: A Cross-Sectional Study
Author(s) -
Melissa Amyx,
Fernando Althabe,
Julie Rivo,
Verónica Pingray,
Nicole Minckas,
María Belizán,
Luz Gibbons,
Gerardo T Murga,
Angel Fiorillo,
Julio D Malamud,
Roberto Casale,
Gabriela Cormick,
José M. Belizán
Publication year - 2021
Publication title -
maternal and child health journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1
H-Index - 85
eISSN - 1573-6628
pISSN - 1092-7875
DOI - 10.1007/s10995-020-03073-4
Subject(s) - medicine , randomized controlled trial , caesarean section , informed consent , cross sectional study , randomization , population , vaginal delivery , obstetrics , family medicine , gynecology , pregnancy , alternative medicine , environmental health , surgery , genetics , pathology , biology
Though interest is growing for trials comparing planned delivery mode (vaginal delivery [VD]; cesarean section [CS]) in low-risk nulliparous women, appropriate study design is unclear. Our objective was to assess feasibility of three designs (preference trial [PCT], randomized controlled trial [RCT], partially randomized patient preference trial [PRPPT]) for a trial comparing planned delivery mode in low-risk women.

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