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ID06845215

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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who underwent abdominoplasty and received TAP or ESP blocks for postoperative analgesia, followed by monitoring with IV PCA.
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

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

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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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