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 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07478692
Eligibility Criteria:
Inclusion Criteria:
* Aged 20-40 years, in good general health
* ASA physical status I-II
* Singleton, term (37-41 weeks) pregnancy with normal fetal development
* Planned for elective cesarean section, no labor
Exclusion Criteria:
* Pregnancy complications (e.g., severe preeclampsia, gestational diabetes, placental abruption)
* Major organ dysfunction (heart, liver, kidney) or psychiatric history
* Allergy to local anesthetics or any study drugs
* Prior abdominal surgery or infection that may affect block efficacy
* Coagulation disorders or current anticoagulant use
* Refusal to participate or inability to comply with follow-up
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT07478692
Study Brief:
Protocol Section:
NCT07478692