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Clinical Trial Summary

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


Clinical Trial Description

Patients undergone to primary total knee replacement with spinal anesthesia are randomized to receive a continuous adductor canal block infusion + an ipack block or a continuous femoral nerve block + a continuous sciatic nerve block just at the end of surgery. Both group will receive a multimodal analgesia with paracetamol, ketorolac, desametasone and morphine as a rescue. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06182059
Study type Interventional
Source Policlinico di Monza SpA
Contact Gianluca Cappelleri, MD
Phone +390392810941
Email gianluca.cappelleri@policlinicodimonza.it
Status Recruiting
Phase N/A
Start date January 12, 2024
Completion date July 31, 2025

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