Induction of labor in maternal and fetal condition Induction of labor ,
Conditions
Interventions
given 12.5 micrograms of misoprostol oral every 2 hr,given 25 micrograms of misoprostol oral every 2 hr
Experimental Drug,Experimental Drug
12.5 micrograms of misoprostol,25 micrograms of misoprostol
Sponsors
Udonthani hospital
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: women with singleton live pregnancy , Gestational age greater than or equal to 38 weeks , have indication of induction of labor , vertex presentation, normal fetal heart rate , Bishop score less than or equal to 6 point , intact membrane
Exclusion criteria
Exclusion criteria: refuse participate in research , misoprostol allergy , previous cesarean section or myomectomy ,underlying disease such as heart, renal ,liver disease ,severe preeclampsia with severe feature , Grand multiparity ,regular uterine contraction , multifetal pregnancy , active genital tract disease , DFIU and fetal anomaly , estimate fetal weight more than 4000 grams
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of successful induction of labor within 24 hours , comparing 12.5 and 25 µg oral misoprostol Induction time to delivery time successful induction of labor was defined as vaginal delivery within 24 hr can be achieved | — |
Secondary
| Measure | Time frame |
|---|---|
| maternal and neonatal outcome after delivery period analyzed data of maternal and neonatal outcome after delivery,rate of uterine tachysystole , rate of cesarean section after delivery period record data and analyzed data after delivery | — |
Countries
Thailand
Contacts
Public ContactChutinan Chantarakhantee
Udonthani hospital
Outcome results
None listed