Clinical Trials Directory

Trials / Completed

CompletedNCT06905574

Surgeon-Guided Serratus Block in Breast Reduction Surgery

Postoperative Analgesic Efficacy of Intraoperative Surgeon-Guided Serratus Block: A Prospective Randomized Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
alperen can kokten · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

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

Interventions

TypeNameDescription
OTHERsurgeon guided serratus blockSurgeon guided Serratus Block will be applied before closing dermoglandular flaps

Timeline

Start date
2024-12-01
Primary completion
2025-10-30
Completion
2025-10-31
First posted
2025-04-01
Last updated
2026-01-29

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06905574. Inclusion in this directory is not an endorsement.

Surgeon-Guided Serratus Block in Breast Reduction Surgery (NCT06905574) · Clinical Trials Directory