Clinical Trial

Intrathecal Morphine vs Transversalis Fascia Plane Block After Cesarean Delivery

Completed
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Summary
This prospective single-center study compares intrathecal morphine and ultrasound-guided bilateral transversalis fascia plane block for postoperative analgesia in patients undergoing elective cesarean delivery under spinal anesthesia. The primary outcome is the number of parturients requiring rescue analgesia within the first 24 hours postoperatively. The secondary outcomes include postoperative pain scores, rescue analgesia requirement, nausea/vomiting, pruritus, and obstetric quality of recovery (ObsQoR-11).
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2026-01-20; most recent amendment 2026-05-09.
Status change: Not Yet Recruiting → Completed 2026-03-18
Trial Details
NCT Number NCT07374133
Lead Sponsor Ondokuz Mayıs University
Conditions Cesarean Delivery, Postoperative Analgesia, Obstetric Anesthesia
Enrollment 60 participants
Start Date 2026-02-01
Primary Completion 2026-03-15 (estimated)
Study Completion 2026-03-15 (estimated)
Updated on ClinicalTrials.gov 2026-05-13