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 @ 2:03 AM
Ignite Modification Date:
2025-12-25 @ 2:03 AM
NCT ID:
NCT05271760
Eligibility Criteria:
Inclusion Criteria:
* Multiparous parturients
* ASA physical status II,
* Full-term singleton fetus
* Vertex presentation requesting analgesia during labor.
* Active labor, 4 to 5 cm dilated cervix
Exclusion Criteria:
* Patients with contraindications to regional anesthesia
* Complicated pregnancies
* Primiparous parturients
* Diagnosed fetal abnormalities
* Allergy to the study medications
* INR \>1.3, and or platelets count \<100,000
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT05271760
Study Brief:
Protocol Section:
NCT05271760