Actively Recruiting
US-Guided Quadro-Iliac Plane Block for Postoperative Analgesia After Lumbar Instrumentation
Led by Bursa City Hospital · Updated on 2026-03-06
80
Participants Needed
1
Research Sites
23 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Lumbar instrumentation surgery is associated with significant postoperative pain. This study evaluates the analgesic effectiveness of the ultrasound-guided Quadro-Iliac Plane Block in patients undergoing lumbar instrumentation surgery, aiming to assess the efficacy of this newly developed technique for postoperative pain management.
CONDITIONS
Official Title
US-Guided Quadro-Iliac Plane Block for Postoperative Analgesia After Lumbar Instrumentation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 65 years
- Classified as American Society of Anesthesiologists (ASA) physical status I-III
- Scheduled for elective lumbar instrumentation surgery
- Surgery performed under general anesthesia
- Provided written informed consent
You will not qualify if you...
- Use of anticoagulant or antiplatelet medications
- Presence of bleeding or coagulation disorders
- Known allergy to local anesthetics or opioids
- Infection at the planned block site
- Alcohol or drug dependence
- Cognitive impairment preventing reliable pain assessment
- Pregnancy or lactation
- History of previous lumbar spine surgery
- Diabetes mellitus
- Kidney or liver impairment
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Bursa City Hospital
Bursa, Turkey (Türkiye), 16110
Actively Recruiting
Research Team
M
Mursel Ekinci, Assoc prof,MD
CONTACT
M
Merih Yıldız Eglen, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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