Clinical Trial

Serratus vs ESP Block for Postoperative Pain in Unilateral Breast Surgery

Recruiting
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Summary
This prospective, randomized, assessor-blinded trial compares serratus posterior superior intercostal plane block (SPSIPB) and erector spinae plane block (ESPB) for postoperative analgesia in unilateral breast surgery. 54 patients will be randomized to receive either SPSIPB or ESPB before general anesthesia. The primary outcome is postoperative pain scores within the first 24 hours. The secondary outcome is opioid consumption.
Protocol Amendment History 3 changes
notable Primary completion pushed: 2026-08-01 -> 2026-09-01 2026-08-07
minor Completion pushed: 2026-08-01 -> 2026-09-01 2026-08-07
critical Recruitment opened 2026-06-24
Trial Details
NCT Number NCT07541040
Lead Sponsor Engin Çetin
Conditions Post Operative Pain, Opioid Use
Enrollment 54 participants
Start Date 2026-05-01
Primary Completion 2026-09-01 (estimated)
Study Completion 2026-09-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-06