About this trial
The primary objective of this study is to evaluate and compare the efficacy of different volumes of local anesthetics, administered at the same total dose, for ilioinguinal and iliohypogastric (II/IH) nerve blocks in patients undergoing unilateral inguinal hernia repair.
The investigators aim to determine whether varying the injectate volume-while keeping the total drug amount constant-influences the quality and duration of postoperative analgesia. By monitoring pain scores and opioid consumption, this research seeks to identify the optimal volume-to-dose ratio for enhancing patient recovery and pain management following inguinal surgery.
Eligibility criteria
Qualifiers
Patients aged between 18 and 75 years
American Society of Anesthesiologists (ASA) physical status I, II, or III
Diagnosis of unilateral inguinal hernia
Scheduled for elective open inguinal hernia repair under spinal anesthesia
Disqualifiers
Age under 18 or over 75 years
ASA physical status IV or higher
Body mass index (BMI) greater than 35 kg/m²
Pregnancy or suspected pregnancy
Trial design
Treatments tested in this trial
- Bupivacaine (Ilioinguinal-iliohypogastric nerve block)