This prospective cohort study aims to determine whether maternal and neonatal outcomes are affected by GBS carrier status in women undergoing transcervical balloon catheter insertion.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
500
induction of labor by transcervical Balloon Catheters insertion
adverse neonatal outcomes
the incidence of composite adverse neonatal outcomes based on the NICE criteria for early detection of neonatal sepsis
Time frame: 2-3 days
composite adverse maternal outcomes
chorioamnionitis, suspected chorioamnionitis or endometritis, urinary tract infection or sepsis in the peripartum period, prolonged hospital stay, and allergic reaction to antibiotics
Time frame: 2-3 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.