Cesarean Section Rate in Oxytocin Infusion between Continuous Until Delivery and Discontinuation at Active Phase of Labor: a Randomized Controlled Study
Phase 4
Completed
- Conditions
- cesarean section rate,neonatal outcomesmaternal complications,laboroxytocin,
- Registration Number
- TCTR20150503001
- Lead Sponsor
- Bhumibol Adulyadej Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 340
Inclusion Criteria
gestational age of 37 to 42 weeks, singleton with cephalic presentation, latent phase of labor, estimated fetal weight < 4000 g by Leopold�s maneuver or ultrasonography and bishop score > 4
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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