Interventional, comparative, randomized, controlled study versus standard treatment, in 3 parallel groups, monocentric, aiming to demonstrate the superiority of preoperative cryoneurolysis versus no procedure, in patients operated on for knee arthroplasty and receiving standard analgesia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
52
Knee arthroscopy will be performed ansd patients will receive standard pain relievers in confomtity with the current practice
Hôpital privé Paul d'Egine
Champigny-sur-Marne, France
90 ° flexion pain 2 days after the arthroscopy
Evaluation of the knee pain at 90° flexion with a visual analogic scale of 100 mm
Time frame: 2 days
90 ° flexion pain 1 day after the arthroscopy
Evaluation of the knee pain at 90° flexion with a visual analogic scale of 100 mm
Time frame: 1 day
90 ° flexion pain 7 days after the arthroscopy
Evaluation of the knee pain at 90° flexion with a visual analogic scale of 100 mm
Time frame: 7 days
90 ° flexion pain 30 days after the arthroscopy
Evaluation of the knee pain at 90° flexion with a visual analogic scale of 100 mm
Time frame: 30 days
90 ° flexion pain 90 days after the arthroscopy
Evaluation of the knee pain at 90° flexion with a visual analogic scale of 100 mm
Time frame: 90 days
pain at rest at Day 1
Knee pain after intervention with a visual analogic scale of 100 mm
Time frame: 1 day
pain at rest at Day 2
Knee pain after intervention with a visual analogic scale of 100 mm
Time frame: 2 days
pain at rest at Day 7
Knee pain after intervention with a visual analogic scale of 100 mm
Time frame: 7 days
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pain at rest at Day 30
Knee pain after intervention with a visual analogic scale of 100 mm
Time frame: 30 days
pain at rest at Day 90
Knee pain after intervention with a visual analogic scale of 100 mm
Time frame: 90 days