Actively Recruiting
Persistent Post Surgical Pain After Total Knee Arthroplasty
Led by Policlinico di Monza SpA · Updated on 2025-06-03
436
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Patients undergone total knee replacement are randomized to receive a "fast track" regional anesthesia protocol or a "traditional" regional anesthesia continuous infusion by both a femoral and sciatic catheter to assess if this latter technique may reduce persistent postoperative pain six months after surgery
CONDITIONS
Official Title
Persistent Post Surgical Pain After Total Knee Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary total knee replacement with a written informed consent
You will not qualify if you...
- Allergy to local anesthetics or any drugs involved in the study
- Contraindication to regional anesthesia
- Chronic use of opioids
- Body mass index greater than 35 kg/m2
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Policlinico di Monza SPA
Monza, Monza Brianza, Italy, 20900
Actively Recruiting
Research Team
G
Gianluca Cappelleri, MD
CONTACT
G
Gianluca Perseghin, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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