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Persistent Post Surgical Pain After Total Knee Arthroplasty

P

Policlinico di Monza SpA

Status

Enrolling

Conditions

Knee Arthropathy

Treatments

Procedure: continuous peripheral nerve block

Study type

Interventional

Funder types

Other

Identifiers

NCT06182059
PPSP PTG

Details and patient eligibility

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

Full 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.

Enrollment

436 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

436 participants in 2 patient groups

fast track
Active Comparator group
Description:
continuous adductor canal block and ipack block
Treatment:
Procedure: continuous peripheral nerve block
traditional
Experimental group
Description:
continuous femoral nerve block and continuous sciatic block
Treatment:
Procedure: continuous peripheral nerve block

Trial contacts and locations

1

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Central trial contact

Gianluca Perseghin, MD; Gianluca Cappelleri, MD

Data sourced from clinicaltrials.gov

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