The purpose of this study is to compare the efficacy for cervical ripening in labor induction between titrated and conventional oral misoprostol
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
64
misoprostol 50 micrograms oral every 4 hours until cervical dilatation 3 cm
misoprostol 20 micrograms oral every hours until cervical dilatation 3 cm
Siriraj Hospital, Mahidol University
Bangkok, Bangkok, Thailand
success rate of cervical ripening in labor induction
Time frame: 12 hours after intervention
number of vaginal delivery
Time frame: 24 hours
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