Persistent Post Surgical Pain After Total Knee Arthroplasty
Recruiting
N/A
Interventional Study
Knee Arthropathy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 85
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 436 (estimated)
- Sponsor
- Policlinico di Monza SpA · Other
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About This Trial
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
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* primary total knee replacement with a written informed consent
Exclusion Criteria:
* Allergy to local anesthetics or any drugs involve in the study
* Controindication to regional anesthesia
* chronic use of opioids
* BMI \> 35 kg m2
Contacts