Comparing two pain management techniques after tummy tuck surgery
Comparison of the Efficacy of Transversus Abdominis Plane Block and Erector Spinae Plane Block in Postoperative Analgesia Management After Abdominoplasty
This study tests which of two pain management techniques works better for people recovering from tummy tuck surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 60 (estimated) |
| Sex | All |
| Sponsor | Ankara Ataturk Sanatorium Training and Research Hospital Government |
| Locations | 1 site (Ankara, Keçiören) |
| Trial ID | NCT06845215 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two different nerve block techniques, the Transversus Abdominis Plane (TAP) block and the Erector Spinae Plane (ESP) block, in managing postoperative pain for patients who have undergone abdominoplasty. By monitoring patients who received these blocks along with intravenous patient-controlled analgesia (IV PCA), the study aims to determine which technique provides better pain relief. The research addresses a significant concern in cosmetic surgery, where effective pain management can enhance recovery and patient satisfaction.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who are scheduled to undergo abdominoplasty and will receive either TAP or ESP blocks for postoperative pain management.
Not a fit: Patients who do not receive IV PCA or have complications during the procedure may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing abdominoplasty, enhancing their recovery experience.
How similar studies have performed: Previous studies have shown promising results for both TAP and ESP blocks in managing postoperative pain, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients who underwent abdominoplasty and received TAP or ESP blocks for postoperative analgesia, followed by monitoring with IV PCA. Exclusion Criteria: * Cases in which IV PCA was not used, VAS scoring was unavailable, or complications occurred.
Where this trial is running
Ankara, Keçiören
- University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital — Ankara, Keçiören, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Erbil Türksal, Specialist — University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital
- Study coordinator: ERBİL TÜRKSAL, Specialist
- Email: drerbilturksal@hotmail.com
- Phone: 530 228 1319
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.