Induction methods for healthy pregnant women beyond due day
Conditions
Interventions
Group 1: Cervixpriming with cook cervical ballon
Group 2: Cervixpriming with cook cervical ballon and 3x 1000mg of evening primrose oil oral
Group 3: Cervixpriming with cook cervical ballon and 3x 100
Sponsors
JKU Linz, Medizinische Fakultät
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: • due date +7days until +14 days • healthy pregnancy, also gestational diabetes (if 95% of all sugar measurements of the last two weeks are normal) • Consent to participate in the study • Fetus in cephalic presentation • successful and inconspicuous organ screening
Exclusion criteria
Exclusion criteria: • St.p. Sectio • St.p. documented induction complications in previous pregnancies • fetal abnormalities • PROM • Allergy to evening primrose oil
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the duration between cervical priming and the onset of contraction and delivery. The data is recruited from the birth documentation after delivery and collected in a database. | — |
Secondary
| Measure | Time frame |
|---|---|
| Other secondary objectives are a comparison of complications peri- and postpartum as well as possible influencing factors on the effectiveness between the groups. | — |
Countries
Austria
Contacts
Public ContactAnna Dückelmann
JKU Linz, Medizinische Fakultät
Outcome results
None listed