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 @ 3:13 AM
Ignite Modification Date:
2025-12-25 @ 3:13 AM
NCT ID:
NCT02758405
Eligibility Criteria:
Inclusion Criteria:
* ASA 2 or 3
* Full term (≥ 37 weeks gestation)
* Nulliparous
* Singleton pregnancy, vertex presentation
* Active labor: regular painful contractions occurring at 3-at least every 5 minutes and change in cervix
* Verbal Numerical Pain Score (VNPS) at requesting analgesia \> 5 (VNPS 0-10)
* Cervical dilatation ≥2 ≤ 5 cm
Exclusion Criteria:
* Refusal to provide written informed consent.
* Any contraindication to epidural anesthesia
* Unintentional dural puncture
* Allergy or hypersensitivity to bupivacaine or fentanyl
* Use of opioids or sedatives within the last 4 hours.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
16 Years
Maximum Age:
55 Years
Study:
NCT02758405
Study Brief:
Protocol Section:
NCT02758405