Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:36 PM
Ignite Modification Date:
2025-12-24 @ 7:36 PM
NCT ID:
NCT03025503
Eligibility Criteria:
Inclusion Criteria:
* Week 37 + 0 and on
* PROM (premature rupture of membranes)
* Multiparity (birth sixth or higher) or TOLAC (trial of labor after Caesarean section)
* Not in active labor - without regular contractions fetal monitor, cervical dilation \< 4 cm and effacement \< 80%.
Exclusion Criteria:
* Water break \> 24 hours at the time of admission to the delivery room
* Active vaginal bleeding with suspected placental abruption
* Maternal fever
* Multifetal pregnancy
* Women with contraindication for vaginal birth
* Preeclampsia
* IUGR (intrauterine growth restriction)
* Macrosomia
* Non-reassuring fetal heart tracing
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT03025503
Study Brief:
Protocol Section:
NCT03025503