Official Title
Laparoscopic Inguinal Hernia Surgery Patients: Comparison of Modified Thoracoabdominal Nerve Block Through Perichondrial Approach (M-TAPA) and Oblique Subcostal TAP Block for Postoperative Analgesia
Brief Summary

This randomized controlled trial aims to compare the postoperative analgesic efficacy ofM-TAPA block and OSTAP block in patients undergoing laparoscopic inguinal hernia repair.Pain scores, analgesic consumption, and patient satisfaction will be evaluated.

Detailed Description

Prospective, randomized, single-blind, controlled study including 90 patients undergoing
elective laparoscopic inguinal hernia repair. Patients will be randomized into three
groups: M-TAPA, OSTAP, and control. Postoperative pain scores (VAS), analgesic
consumption, time to first analgesic requirement, and patient satisfaction will be
assessed over 24 hours.

Completed
Inguinal Hernia Bilateral
Postoperative Pain

Procedure: Modified Thoracoabdominal Nerve Block Through Perichondrial Approach (M-TAPA)

Ultrasound-guided bilateral M-TAPA block performed with 20 mL of 0.25% bupivacaine per
side

Procedure: Oblique Subcostal Transversus Abdominis Plane Block (OSTAP)

Ultrasound-guided bilateral OSTAP block performed with 20 mL of 0.25% bupivacaine per
side

Other: Standard Analgesia use (paracetamol, contramal)

Patients received standard postoperative analgesia without regional block

Eligibility Criteria

Inclusion Criteria:

- Patients aged between 18 and 65 years

- American Society of Anesthesiologists (ASA) physical status I-II

- Scheduled for elective laparoscopic inguinal hernia repair (TEP technique)

- Ability to understand and use the Visual Analog Scale (VAS)

- Provided written informed consent

Exclusion Criteria:

- Refusal to participate or inability to provide informed consent

- Age under 18 or over 65 years

- ASA physical status ≥ III

- Coagulopathy (including abnormal INR, thrombocytopenia, or platelet dysfunction)

- Infection at the injection site

- Known allergy or hypersensitivity to study medications (local anesthetics, NSAIDs,
opioids)

- Chronic opioid use (longer than 4 weeks)

- Use of psychiatric medications affecting pain perception

- Inability to cooperate or communicate effectively

- Requirement for postoperative intensive care

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 65 Years
Countries
Turkey (Türkiye)
Locations

Kartal Dr. Lütfi Kırdar City Hospital
Istanbul, Turkey (Türkiye)

Tahsin Simsek, MD, Principal Investigator
Kartal Dr. Lütfi Kirdar City Hospital

Dr. Lutfi Kirdar Kartal Training and Research Hospital
NCT Number
Keywords
MTAPA
OSTAP
postoperative pain
tap block
VAS Score
MeSH Terms
Pain, Postoperative
Acetaminophen
Tramadol