Actively Recruiting
Enhanced Recovery After Surgery and Total Knee Replacement: A Prospective, Randomized Study on the Role of Peripheral Nerve Blocks on Persistent Postoperative Pain Six Months After Surgery
Led by Policlinico di Monza SpA · Updated on 2025-06-03
436
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research evaluates pain management approaches in patients undergoing primary total knee replacement surgery. It compares two regional anesthesia techniques to see if one method reduces persistent postoperative pain six months after surgery. The trial is randomized and sponsored by Policlinico di Monza SpA, focusing on improving recovery and pain outcomes after knee arthropathy surgery. Participants receive either a continuous adductor canal block plus an ipack block or a continuous femoral nerve block combined with a continuous sciatic nerve block immediately after surgery. Both groups are given additional pain relief medications including paracetamol, ketorolac, dexamethasone, and morphine as needed. These interventions are aimed at assessing differences in pain control effectiveness over time. During the study, patients are monitored for persistent post surgical pain up to six months after surgery. Researchers also measure acute pain and morphine use during the first 72 hours post operation. The trial includes assessments of pain levels and medication requirements to track recovery progress. The total duration of participation extends through these follow-up periods to evaluate long-term pain outcomes and treatment impact.
CONDITIONS
Brief Title
Persistent Post Surgical Pain After Total Knee Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary total knee replacement
- Written informed consent provided
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
- BMI over 35 kg/m2
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 72 hours
Participants undergo total knee replacement surgery with spinal anesthesia and receive either a continuous adductor canal block plus an ipack block or a continuous femoral nerve block plus a continuous sciatic nerve block. Multimodal analgesia is provided during this period.
Continuous monitoring during hospital stay post-surgery
Duration - 6 months
Participants are followed to assess persistent post surgical pain and recovery progress after surgery.
Follow-up visits at intervals over 6 months
Trial Site Locations
Total: 1 location
1
Policlinico di Monza SPA
Monza, Monza Brianza, Italy, 20900
Actively Recruiting
Research Team
G
Gianluca Cappelleri, MD
G
Gianluca Perseghin, MD
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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