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 @ 10:51 PM
Ignite Modification Date:
2025-12-24 @ 10:51 PM
NCT ID:
NCT06344169
Eligibility Criteria:
Inclusion Criteria:
* term primipara or multipara who are scheduled for elective cesarean section
Exclusion Criteria:
1. Severe pregnancy-induced complication (such as preeclampsia, eclampsia, poorly control pregnancy-induced hypertension and/or diabetes)
2. High risk for postpartum hemorrhage
3. Contraindicated for neuraxial block
4. Preterm (gestational age\< 36 week) delivery
5. Emergency cesarean section
6. After-office hour schedule
7. History of substance abuse
8. Known allergy to nalbuphine, benzyl benzoate or sesame oil
9. Eligible parturient who are not willing to follow the assignment of treatment after randomization
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Study:
NCT06344169
Study Brief:
Protocol Section:
NCT06344169