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 @ 12:09 AM
Ignite Modification Date:
2025-12-25 @ 12:09 AM
NCT ID:
NCT06178458
Eligibility Criteria:
Inclusion Criteria:
* Patients who had at least 2 cesarean deliveries
* Patients received spinal anesthesia and intrathecal morphine for cesarean delivery
* Patients received postoperative pain control as per standard protocol
Exclusion Criteria:
* Patients with chronic pain prior to cesarean delivery
* Unable to give pain score
* Receiving general anesthesia for cesarean delivery
* Receiving postoperative pain control beyond the standard protocol
* Patients with multiple pregnancy, placenta abruption, placenta accrete, postpartum hemorrhage
* Patients with psychotic disorder
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06178458
Study Brief:
Protocol Section:
NCT06178458