About this trial
Inguinal hernia repair is one of the most commonly performed surgical procedures. It is generally performed under regional anesthesia techniques, such as local anesthesia, peripheral nerve blocks, or neuraxial anesthesia (spinal or epidural anesthesia), or under general anesthesia. Despite various available analgesic regimens, numerous studies have demonstrated that postoperative pain control remains inadequate. Opioids, nonsteroidal anti-inflammatory drugs, and analgesics are frequently used for postoperative pain management. However, these medications are associated with uncertain efficacy and undesirable side effects. Pain is a critical factor in the postoperative period, contributing to delayed ambulation and paralytic ileus, ultimately hindering early discharge.
Eligibility criteria
Qualifiers
Patients aged 18-65 years
Undergoing elective,
unilateral laparoscopic inguinal hernia repair
Receiving general anesthesia
Disqualifiers
Patients who refuse to provide consent
Patients with contraindications to regional anesthesia
Patients with impaired consciousness
Patients with coagulopathy
Trial design
Treatments tested in this trial
- Quadro iliac plane block
- Control group