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 @ 9:55 PM
Ignite Modification Date:
2025-12-24 @ 9:55 PM
NCT ID:
NCT06221332
Eligibility Criteria:
Inclusion Criteria:
* 36-42. Pregnant women who are their gestational age and request epidural anesthesia
* Pregnant women aged 18-42 with ASA II
* Pregnant women who will stay in the hospital for at least 24 hours
* Primiparous pregnant women who will have a planned normal birth
* Singleton births with vertex presentation
Exclusion Criteria:
* Pregnant women who do not want to give consent
* Regional anesthesia is contraindicated
* Pregnant women who use anticoagulants and have an abnormal bleeding profile
* Pregnant women with infection in the area to be treated
* Emergency cases and pregnant women who had a birth with instruments (forceps and vacuum)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
42 Years
Study:
NCT06221332
Study Brief:
Protocol Section:
NCT06221332