Actively Recruiting
Ultrasound-Guided Quadro-Iliac Plane Block for Pain Management After Total Hip Arthroplasty
Led by Bursa City Hospital · Updated on 2026-03-27
100
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective, randomized, double-blind study evaluates the analgesic effectiveness of the ultrasound-guided Quadro-Iliac Plane (QIP) block in patients undergoing primary total hip arthroplasty. The QIP block is a recently described fascial plane block. Patients will be randomized to receive either a QIP block with local anesthetic or a sham block with saline. The primary outcome is 24-hour opioid consumption. Secondary outcomes include motor block, dermatomal sensory assessment, pain scores, rescue analgesic requirement, quality of recovery (QoR-15), and opioid-related side effects.
CONDITIONS
Official Title
Ultrasound-Guided Quadro-Iliac Plane Block for Pain Management After Total Hip Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 80 years
- American Society of Anesthesiologists (ASA) classification I-III
- Patients scheduled for elective primary total hip arthroplasty
You will not qualify if you...
- Refusal to participate in the study
- Allergy to local anesthetics or opioids
- Known or suspected coagulopathy
- Infection at the injection site
- History of previous hip surgery
- Severe cardiovascular disease
- Liver or kidney failure
- Pregnancy, suspected pregnancy, or breastfeeding
- Severe neurological or psychiatric disorder
- Chronic opioid use
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
Mustafa Dikici, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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