QIPB in Inguinal Hernia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorKonya City Hospital

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

Treatment groups

70 Participants
are divided into 2 treatment groups

Sponsors and collaborators