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 @ 2:28 PM
Ignite Modification Date:
2025-12-24 @ 2:28 PM
NCT ID:
NCT02344459
Eligibility Criteria:
Inclusion Criteria:
* Bishop score of 5 or less
* Singleton
* Cephalic presentation
* Fewer than 4 contractions in 10 minutes
* Reactive fetal monitoring
Exclusion Criteria:
* Non-vertex presentation
* Placenta previa
* Vasa previa
* Unexplained vaginal bleeding
* Active herpes simplex virus infection
* Non-English speaking
* Previous attempt at an induction of labor in the current pregnancy
* Prolapsed umbilical cord
* More than one prior cesarean delivery or history of classical cesarean delivery
* Patients receiving or planning to undergo exogenous prostaglandin administration as the primary induction agent
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT02344459
Study Brief:
Protocol Section:
NCT02344459