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 @ 2:40 AM
Ignite Modification Date:
2025-12-25 @ 2:40 AM
NCT ID:
NCT05499234
Eligibility Criteria:
Inclusion Criteria:
* ASA II primigravid women
* with cervical dilatation between 4-6 cm, demanding epidural analgesia during spontaneous vaginal delivery
Exclusion Criteria:
* Participants with pregnancy-related diseases
* gestational hypertension
* gestational diabetes
* preeclampsia/ celmpsia
* contraindications for neuraxial block
* infection
* coagulation disorders
* severe hypovolemia
* sepsis
* neurological deficit
* cardiac valve stenosis or hypertrophic obstructive cardiomyopathy
* Women with fetal malpresentation and fetal anomaly
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT05499234
Study Brief:
Protocol Section:
NCT05499234