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
| Type | Name | Description |
|---|---|---|
| OTHER | surgeon guided serratus block | Surgeon 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.