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Surgeon-Guided Serratus Block in Breast Reduction Surgery

NCT06905574 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2026-01-29

No results posted yet for this study

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.

Conditions

  • Postoperative Pain Control
  • Breast Reduction

Interventions

OTHER

surgeon guided serratus block

Surgeon guided Serratus Block will be applied before closing dermoglandular flaps

Sponsors & Collaborators

  • alperen can kokten

    lead OTHER

Principal Investigators

  • Ayhan Sönmez · SAMSUN UNİVERSİTY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-12-01
Primary Completion
2025-10-30
Completion
2025-10-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06905574 on ClinicalTrials.gov