induction of labor at term
Conditions
Interventions
dinoprostone pessary group and misoprostol vaginal tablet group:Not applicable
Sponsors
Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: age > 18 years, >= 37 weeks, singleton, cephalocephaly, need to promote cervical ripening (Bishop < 6), parity < 3, non scarred uterus
Exclusion criteria
Exclusion criteria: who did not use misoprostol vaginal tablet or dinoprostone for induction of labor, contraindications to vaginal trial production, breech presentation, allergy to prostaglandins or severe asthma reaction, and incomplete data were exclude.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cesarean section rate;elivery 24 hours after medication; | — |
Secondary
| Measure | Time frame |
|---|---|
| hypercontractions,;whether other methods of induction need to be sequential;whether amniotic fluid fecal staining;whether intrapartum fever;whether episiotomy; whether severe perineal laceration (? - ? degrees);whether uterine rupture;whether postpartum hemorrhage, ;whether neonatal asphyxia;Apgar score;neonatal blood gas analysis;whether newborns need to be admitted to NICU (cause, diagnosis);whether newborns die;whether mothers die; | — |
Countries
China
Contacts
Public ContactWeizhen Jiang
Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Outcome results
None listed