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Clinical Trials/NCT07290881
NCT07290881
Recruiting
Not Applicable

A Prospective Randomized Study Comparing the Postoperative Analgesic Efficacy of Anterior Iliac Block and Ilioinguinal-iliohypogastric Block in Inguinal Hernia Surgery

Harran University1 site in 1 country60 target enrollmentStarted: April 20, 2026Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Akut ağrı (Sayısal Derecelendirme Ölçeği-NRS)

Overview

Brief Summary

The primary aim of this study is to compare two postoperative analgesia techniques used in patients undergoing inguinal hernia surgery-(1) the anterior iliac block and (2) the ilioinguinal/iliohypogastric block-in terms of postoperative analgesia duration and patient satisfaction.

Effective postoperative analgesia in inguinal hernia surgery is crucial for improving patient comfort and reducing opioid consumption. Although ilioinguinal and iliohypogastric nerve blocks are commonly used for this purpose, their relatively limited dermatomal coverage may result in inadequate analgesia in some cases. The recently described Anterior Iliac Block has been proposed as an alternative to conventional techniques, offering potentially wider neural spread and more effective postoperative pain control. However, the efficacy and safety of this novel block have not yet been sufficiently evaluated in the literature.

Detailed Description

The primary aim of this study is to compare two postoperative analgesia techniques used in patients undergoing inguinal hernia surgery-(1) the anterior iliac block and (2) the ilioinguinal/iliohypogastric block-in terms of postoperative analgesia duration and patient satisfaction.

Effective postoperative analgesia in inguinal hernia surgery is crucial for improving patient comfort and reducing opioid consumption. Although ilioinguinal and iliohypogastric nerve blocks are commonly used for this purpose, their relatively limited dermatomal coverage may result in inadequate analgesia in some cases. The recently described anterior iliac block has been proposed as an alternative to conventional techniques, offering potentially wider neural spread and more effective postoperative pain control. However, the efficacy and safety of this novel block have not yet been sufficiently evaluated in the literature.

This study aims to compare the anterior iliac block with the ilioinguinal/iliohypogastric block in terms of postoperative pain control and patient satisfaction. The objective is to determine whether the anterior iliac block, through its broader dermatomal distribution, provides lower NRS pain scores, reduced analgesic requirements, and higher patient satisfaction compared with traditional nerve blocks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • It includes patients aged 18-65 years
  • Classified as ASA I-II
  • Who are undergoing elective inguinal hernia surgery

Exclusion Criteria

  • Patients who did not wish to participate voluntarily
  • Those with contraindications to the anterior iliac block or the Ilioinguinal/Iliohypogastric block,
  • Pregnant or breastfeeding women
  • Patients classified as ASA III-IV-V

Arms & Interventions

Patient group who underwent anterior iliac block

Active Comparator

In this patient group, an anterior iliac block will be administered in the postoperative period, and postoperative pain at the surgical site will be assessed.

Intervention: Patient group who underwent anterior iliac block (Other)

Patient group who underwent ilioinguinal-iliohypogastric block

Active Comparator

In this patient group, an ilioinguinal-iliohypogastric block will be administered in the postoperative period, and postoperative pain at the surgical site will be assessed.

Intervention: Patient group who underwent ilioinguinal/iliohypogastric block (Other)

Outcomes

Primary Outcomes

Akut ağrı (Sayısal Derecelendirme Ölçeği-NRS)

Time Frame: 0-1-3-6-12-24 Hours

The score is rated on a scale from 0 to 10, where 0 indicates no pain and 10 indicates unbearable pain.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

ABDULHAKİM ŞENGEL

SPECİALİST, MD, ANESTHESİOLOGY AND REANİMATİON

Harran University

Study Sites (1)

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