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NCT Number: NCT07290881

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Harran University

Şanliurfa, Hali̇li̇ye, 63040, Turkey (Türkiye)

Location status: Recruiting

Location contact

Abdulhakim Şengel

CONTACT

[email protected]

05374030916

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Patient group who underwent ilioinguinal/iliohypogastric block

Other

Patient group who underwent ilioinguinal/iliohypogastric block

Patient group who underwent anterior iliac block

Other

Patient group who underwent anterior iliac block

Primary outcomes

  1. 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.

Sponsors and collaborators

Lead sponsor

Harran University

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Dec 18, 2025
Registry last updated
Apr 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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