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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• It includes patients aged 18-65 years

• Classified as ASA I-II

• Who are undergoing elective inguinal hernia surgery

Locations
Other Locations
Turkey
Harran University
RECRUITING
Şanliurfa
Time Frame
Start Date: 2026-04-20
Estimated Completion Date: 2026-09-01
Participants
Target number of participants: 60
Treatments
Active_comparator: Patient group who underwent anterior iliac block
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.
Active_comparator: Patient group who underwent ilioinguinal-iliohypogastric block
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.
Related Therapeutic Areas
Sponsors
Leads: Harran University

This content was sourced from clinicaltrials.gov