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 @ 9:57 PM
Ignite Modification Date:
2025-12-24 @ 9:57 PM
NCT ID:
NCT02993432
Eligibility Criteria:
Inclusion Criteria:
* Nulliparous women 37 weeks and 0 days to 41 weeks and 6 days gestational age (term) requiring cervical ripening
* Health care provider feels it is possible to administer either method of cervical ripening.
* Bishop score of 6 or less
* Live, singleton, cephalic fetus
* Availability of personnel to consent and randomize participants
Exclusion Criteria:
* Non-viable fetus
* Contraindication to cervical ripening, labour induction or labour
* Prior attempt at induction of labour in this pregnancy
* Spontaneous rupture of fetal membranes
* Evidence of labour or regular uterine contractions
* Lack of consent
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT02993432
Study Brief:
Protocol Section:
NCT02993432