Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07290881

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

Led by Harran University · Updated on 2026-04-21

60

Participants Needed

1

Research Sites

19 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 65 years
  • Classified as ASA I or II
  • Undergoing elective inguinal hernia surgery
Not Eligible

You will not qualify if you...

  • Patients who do not wish to participate voluntarily
  • Contraindications to anterior iliac block or ilioinguinal/iliohypogastric block
  • Pregnant or breastfeeding women
  • Classified as ASA III, IV, or V

AI-Screening

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Trial Site Locations

Total: 1 location

1

Harran University

Şanliurfa, Hali̇li̇ye, Turkey (Türkiye), 63040

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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