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:
2026-03-26 @ 3:19 PM
Ignite Modification Date:
2026-03-26 @ 3:19 PM
NCT ID:
NCT07395934
Eligibility Criteria:
Inclusion Criteria:
* Parturients indicated for labor analgesia for vaginal delivery via epidural anesthesia.
* Age from 18 to 40 years.
* Physical status: ASA II.
* Singleton pregnancy, full-term, vertex presentation in labor.
* Indication for vaginal delivery.
* No contraindications to epidural anesthesia.
* Agreement to participate in the research and signed written informed consent.
Exclusion Criteria:
* Contraindications to epidural analgesia.
* History of allergy to local anesthetics (Ropivacaine) or opioids (Fentanyl).
* High-risk pregnancies: Preeclampsia, placenta previa, placental abruption.
* Fetal distress or fetal abnormalities.
* Chronic use of analgesic drugs or neurological/psychiatric disorders.
* Parturients who refuse to participate or request to withdraw from the research.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT07395934
Study Brief:
Protocol Section:
NCT07395934