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Cryoneurolysis Prior to Total Knee Arthroplasty (CRYO-TKA Trial)

Cryoneurolysis Prior to Total Knee Arthroplasty (CRYO-TKA Trial)

Recruiting
18 years and older
All
Phase N/A

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Overview

Approximately 20-30% of patients experience persistent pain after a Total Knee Arthroplasty (TKA). This study investigates whether percutaneous cryoneurolysis of genicular nerves can reduce pain and improve physical function when performed at least 24 hours before surgery. Participants will be randomized to receive either the cryoneurolysis procedure + TKA or TKA only. Results will be tracked for 6 months to see if the intervention improves long-term recovery and quality of life.

Description

The current study is a prospective, single-center, randomized comparative trial (1:1 ratio). In the intervention group, cryoneurolysis is performed under imaging guidance targeting the upper lateral and medial and the lower medial genicular nerves. Under prophylactic antibiosis, and imaging guidance 17Gauge cryoprobes will be percutaneously placed at the level of the upper lateral and medial and the lower medial genicular nerves. The final position of each cryo probe will be verified with imaging guidance. Cryoneurolysis protocol will be 5min freezing-4min passive thawing-5min freezing. Post-interventional imaging will verify lack of potential immediate complications

Eligibility

Inclusion Criteria:

  • Adults ≥18 years undergoing primary TKA for osteoarthritis.
  • Cognitively normal and able to self-assess pain and function.
  • Provide written informed consent.

Exclusion Criteria:

  • Cancer-related knee pain.
  • Neurological, psychiatric, or medical conditions interfering with assessment.
  • Chronic opioid users.

Study details
    Arthroplasty
    Replacement Material
    Knee Arthritis Osteoarthritis
    Knee Arthroplasty
    Total
    Genicular Nerves
    Chronic Pain

NCT07425457

Attikon Hospital

26 February 2026

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