Actively Recruiting
Comparison of the Efficacy of Transversus Abdominis Plane Block and Erector Spinae Plane Block in Postoperative Pain Management After Abdominoplasty
Led by Ankara Ataturk Sanatorium Training and Research Hospital · Updated on 2025-06-15
60
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Abdominoplasty is a surgical procedure that removes extra skin and fat from the abdomen, including tightening of abdominal muscles and repositioning of the belly button. This procedure has become more common, but often leads to significant postoperative pain, with up to 80% of patients affected. Managing this pain effectively is important to help patients move sooner, shorten hospital stays, reduce healthcare costs, and improve satisfaction. This research compares two ultrasound-guided nerve block techniques, the Transversus Abdominis Plane (TAP) block and the Erector Spinae Plane (ESP) block, used to manage pain after abdominoplasty. Patients received either TAP or ESP blocks followed by intravenous patient-controlled analgesia (IV PCA) to help control their pain after surgery. Researchers will review patient records to collect data on pain scores at various times within 24 hours after surgery using a pain rating scale, as well as PCA device use, additional pain medication needs, side effects like nausea or itching, and patient satisfaction. The study aims to understand differences in pain relief between the two nerve block methods after abdominoplasty.
CONDITIONS
Brief Title
Comparison of the Efficacy of Transversus Abdominis Plane Block and Erector Spinae Plane Block in Postoperative Analgesia Management After Abdominoplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who underwent abdominoplasty and received TAP or ESP blocks for postoperative analgesia, followed by monitoring with IV PCA.
You will not qualify if you...
- Cases in which IV PCA was not used.
- Patients lacking pain scoring data.
- Patients with complications during treatment.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Postoperative 24 hours
Participants undergo abdominoplasty surgery and receive either a Transversus Abdominis Plane (TAP) block or an Erector Spinae Plane (ESP) block for postoperative pain management, followed by intravenous patient-controlled analgesia (IV PCA).
1 surgery visit and immediate postoperative monitoring
Trial Site Locations
Total: 1 location
1
University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital
Ankara, Keçiören, Turkey (Türkiye), 06290
Actively Recruiting
Research Team
E
ERBİL TÜRKSAL, Specialist
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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