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:
2025-12-25 @ 5:01 AM
Ignite Modification Date:
2025-12-25 @ 5:01 AM
NCT ID:
NCT07268118
Eligibility Criteria:
Inclusion Criteria:
* Age ≥18 years
* Gestational age ≥37 weeks
* Viable pregnancy
* Intact membranes
* English speaking
* Interested in cervical ripening balloon placement
* Able to provide consent
Exclusion Criteria:
* Allergy or sensitivity to lidocaine
* Patients that already have neuraxial anesthesia (i.e. spinal, epidural, combined spinal/epidural)
* Known uterine or cervical anomalies
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07268118
Study Brief:
Protocol Section:
NCT07268118