Clinical Trial

Surgeon-Guided Serratus Block in Breast Reduction Surgery

Completed
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Summary
Surgeon guided serratus block, which can be performed by the surgeon in participants undergoing breast reduction surgery, may reduce the sensation of pain from the surgical field in the postoperative period. Thus, participants experience less pain in the postoperative period, consume less analgesics, and there is a decrease in related complications. The aim of this study was to evaluate the effects of the intraoperative surgeon guided serratus block applied on the analgesic consumption of the participants in the first 24 hours after surgery in participants undergoing breast reduction surgery.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-03-25.
Status change: Recruiting → Completed 2026-01-28
Trial Details
NCT Number NCT06905574
Lead Sponsor alperen can kokten
Conditions Postoperative Pain Control, Breast Reduction
Enrollment 60 participants
Start Date 2024-12-01
Primary Completion 2025-10-30 (estimated)
Study Completion 2025-10-31 (estimated)
Updated on ClinicalTrials.gov 2026-01-29