Labor induction O48
Conditions
Interventions
Group 1: Misodel® (Misoprostol, vaginal insert)
Group 2: Minprostin gel (Dinoproston, vaginal)
Group 3: Cytotec® (Misoprostol, oral)
Sponsors
Vivantes Klinikum im FriedrichshainGynäkologie und Geburtsmedizin
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: induction of labor with Misodel®, Dinoproston, oral Misoprostol, singleton pregnancy, gestational age =36+0 gestational weeks, age= 18 years, Bishop Score =4 restrospektive study including patients from 01/01/2014 (admission of Misodel®)
Exclusion criteria
Exclusion criteria: previous cesarean delivery, premature rupture of the membranes 48 h before induction, less than 36 + 0 gestational weeks, incomplete dataset, more than 3 previous vaginal deliveries after 24+0 gestational weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of acidotic values in the umbilical artery after induction of labor | — |
Secondary
| Measure | Time frame |
|---|---|
| APGAR - Score, rate of cesarean section, rate of operative vaginal delivery, the prevalence of predelivery oxytocin, rate of pathological fetal heart pattern, rate of uterine tachysystole, umbilical artery pH, umbilical artery base excess, admission to NICU, subgroup analysis of diabetic women, patient satisfaction (standardized questionnaire) | — |
Countries
Germany
Contacts
Public ContactSilke Wegener
Vivantes Klinikum im FreidrichshainGynäkologie und Geburtsmedizin
Outcome results
None listed