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 @ 4:58 AM
Ignite Modification Date:
2025-12-25 @ 4:58 AM
NCT ID:
NCT03232918
Eligibility Criteria:
Inclusion Criteria:
* Healthy nulliparous or multiparous women at term (37 \> weeks' gestation)
* Singleton pregnancy
* Request for neuraxial analgesia
* Oxytocin used for induction of labor or augmentation of labor per institutional protocols
Exclusion Criteria:
* Use of chronic analgesic medications
* Prior administration of systemic opioid labor analgesia
* Non-vertex presentation
* Contraindication to neuraxial analgesia
* Category 3 fetal heart rate tracing prior to the initiation of combined spinal epidural analgesia
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
55 Years
Study:
NCT03232918
Study Brief:
Protocol Section:
NCT03232918