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 @ 3:56 AM
Ignite Modification Date:
2025-12-25 @ 3:56 AM
NCT ID:
NCT07181902
Eligibility Criteria:
Inclusion Criteria
* Women aged 18-45 years, scheduled for elective cesarean delivery under spinal anesthesia.
* Gestational age ≥37 weeks, singleton pregnancy.
* Undergoing either ESP or RLB for postoperative analgesia.
* ASA Physical Status II-III.
* Ability to understand and complete ObsQoR-11T questionnaire.
* Provided written informed consent prior to participation. Exclusion Criteria
* Emergency cesarean delivery.
* Multiple pregnancy, preterm delivery (\<37 weeks),
* Severe maternal or obstetric complications (e.g., preeclampsia, placenta previa, placenta accreta spectrum), regardless of urgency.
* BMI ≥40 kg/m²
* Significant systemic diseases (e.g., severe cardiac, respiratory, renal, or hepatic disease).
* Fetal or placental anomalies.
* History of chronic pain syndromes, opioid dependence, or long-term analgesic use.
* Neurological, psychiatric, or cognitive disorders that may interfere with pain perception or questionnaire completion.
* Patients who declined participation or did not provide informed consent.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07181902
Study Brief:
Protocol Section:
NCT07181902