About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
It includes patients aged 18-65 years
Classified as ASA I-II
Who are undergoing elective inguinal hernia surgery
Disqualifiers
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
Trial design
Parallel
Treatments tested in this trial
Patient group who underwent ilioinguinal/iliohypogastric block
Other interventionPatient group who underwent ilioinguinal/iliohypogastric block
Patient group who underwent anterior iliac block
Other interventionPatient group who underwent anterior iliac block
Treatment groups
Trial outcomes
Primary outcomes
Akut ağrı (Sayısal Derecelendirme Ölçeği-NRS)
The score is rated on a scale from 0 to 10, where 0 indicates no pain and 10 indicates unbearable pain.
Locations
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Sponsors and contacts
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