- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06862609
QIPB in Inguinal Hernia
March 8, 2026 updated by: Muhammed Halit Satici, Konya City Hospital
Effect of the Quadro-Iliac Plane Block on Quality of Recovery Following Laparoscopic Inguinal Hernia Surgery: A Prospective, Randomized, Controlled, Double-Blind, Multicenter Study
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.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
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.
Recently, Tulgar and colleagues introduced a novel fascial plane block known as the "quadro-iliac plane block".
Quadro-iliac plane block is performed within the quadro-iliac plane, located between the inner surface of the iliac crest and the posterior surface of the quadratus lumborum muscle.
In their study, Tulgar et al. bilaterally injected 40 mL of methylene blue into the quadro-iliac plane.
They observed widespread dye dispersion along the anterior and posterior surfaces of the quadratus lumborum muscle, transversalis fascia, ilioinguinal, iliohypogastric, subcostal, and genitofemoral nerves, as well as the lumbar plexus.
Based on these findings, quadro-iliac plane block has been proposed as a potentially effective technique for managing acute or chronic pain in the lumbosacral, abdominal, and hip regions.
Study Type
Interventional
Enrollment (Estimated)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Konya, Turkey (Türkiye)
- Recruiting
- Konya City Hospital
-
Contact:
- Muhammed H SATICI, M.D
- Phone Number: +90 5455636333
- Email: halit_satici@hotmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Patients aged 18-65 years
- Undergoing elective,
- unilateral laparoscopic inguinal hernia repair
- Receiving general anesthesia
Exclusion Criteria:
- 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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: control group
All patients will receive IV paracetamol (1 g, 3×1) and IV tenoxicam (20 mg, 2×1).
Rescue analgesia (IV tramadol 1 mg/kg) will be administered if Numerical rating scale scores are ≥3.
IV ondansetron (4 mg) will be given for nausea and vomiting.
|
Patients in Group Q will be placed in the lateral position.
A low-frequency convex transducer and a 100-mm block needle will be used.
Following sterilization, the transducer will be placed parasagittally at the distal attachment of the quadratus lumborum muscle to the iliac crest.
The iliac crest and quadratus lumborum muscle will be visualized, with the erector spinae muscle above and the psoas major muscle below.
Using an in-plane technique, the needle will be directed toward the iliac crest.
After confirmation with 5 mL of isotonic sodium chloride, 20 mL of 0.25% bupivacaine will be injected incrementally with intermittent aspiration.
The same procedure will be applied to the other party.
A total of 40 mL of 0.25% bupivacaine will be administered.
|
|
Active Comparator: Quadro iliac plane block
All patients will receive IV paracetamol (1 g, 3×1) and IV tenoxicam (20 mg, 2×1).
Rescue analgesia (IV tramadol 1 mg/kg) will be administered if Numerical rating scale scores are ≥3.
IV ondansetron (4 mg) will be given for nausea and vomiting.
Group Q patients will receive quadro iliac plane block in addition to standard analgesia.
|
All patients will receive IV paracetamol (1 g, 3×1) and IV tenoxicam (20 mg, 2×1).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The primary outcome is the QoR-15 score (0-150 point) at 24 hours postoperatively.
Time Frame: 24 hours
|
The primary outcome is the QoR-15 score (0-150 point) at 24 hours postoperatively.
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 23, 2025
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
February 25, 2025
First Submitted That Met QC Criteria
March 3, 2025
First Posted (Actual)
March 6, 2025
Study Record Updates
Last Update Posted (Actual)
March 11, 2026
Last Update Submitted That Met QC Criteria
March 8, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- QIPB İnguinal hernia
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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