Actively Recruiting
QIPB in Inguinal Hernia
Led by Konya City Hospital · Updated on 2026-03-11
70
Participants Needed
1
Research Sites
62 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
QIPB in Inguinal Hernia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-65 years
- Undergoing elective unilateral laparoscopic inguinal hernia repair
- Receiving general anesthesia
You will not qualify if you...
- Patients who refuse to provide consent
- Patients with contraindications to regional anesthesia
- Patients with impaired consciousness
- Patients with coagulopathy
- Patients with infections at the block site
- Emergency cases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Konya City Hospital
Konya, Turkey (Türkiye)
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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