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 @ 10:44 PM
Ignite Modification Date:
2025-12-24 @ 10:44 PM
NCT ID:
NCT03712735
Eligibility Criteria:
Inclusion Criteria:
* Singleton, vertex presentations at term (37-42 weeks gestational age)
* \</= 5cm cervical dilation at the time of epidural anesthesia request
* ASA 2-3 patients aged 19 or over who are able to provide informed consent
Exclusion Criteria:
* Contraindications to neuraxial analgesia or risk factors likely to affect placement or function of the epidural
* History of hypersensitivity or idiosyncratic reaction to local anesthetics or opioids
* Current or historical evidence of any significant medical conditions
* Clinical settings in which continuous epidural infusion may be preferable
* Risk factors significantly increasing the need for Cesarean delivery
* Anticipated fetal abnormalities
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
19 Years
Study:
NCT03712735
Study Brief:
Protocol Section:
NCT03712735