cesarean section rate,
Conditions
Interventions
continued oxytocin group is the group which continue oxytocin infusion for labor induction or augmentation until delivery,discontinued oxytocin group is the group which discontinue oxytocin infusion
Experimental Drug,Placebo Comparator Drug
continued oxytocin group,discontinued oxytocin group
Sponsors
Bhumibol Adulyadej Hospital
Department of Obstetrics and Gynecology,
Bhumibol Adulyadej Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: gestational age of 37 to 42 weeks, singleton with cephalic presentation, latent phase of labor, estimated fetal weight 4
Exclusion criteria
Exclusion criteria: fetal malpresentation, previous cesarean section or uterine scar such as previous myomectomy, placenta previa, placental abruption, persistent non-reassuring fetal heart rate pattern, active phase of labor, premature rupture of membrane (PROM), documented fetal anomalies, severe maternal diseases or maternal complications such as severe pre-eclampsia, diabetes mellitus, heart disease, HIV infection, genital lesions that obstruct passage of labor such as large genital wart or active genital herpes and contracted pelvis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the rate of cesarean section between the parturient in the continued group and discontinued oxytocin 24 hour after enrollment the rate of cesarean section between the parturient in the continued group and discontinued oxytocin | — |
Secondary
| Measure | Time frame |
|---|---|
| duration of each stage of labor 24 hour after enrollment duration of each stage of labor,maternal complications 24 hour after enrollment numbers of cases who had intrapartum complications aor postpartum complications,neonatal outcomes 24 hour after enrollment numbers of cases who had adverse outcomes of neonates | — |
Countries
Thailand
Contacts
Public ContactLalida Chookijkul
Bhumibol Adulyadej Hospital
Outcome results
None listed