The purpose of the study is to evaluate the superiority of Rebel Reliever® knee brace + standard treatment versus standard treatment alone in terms of last 24-hour pain relief after 6 weeks. in patients with medial knee osteoarthritis.
The main criteria is the evaluation of global knee pain during the last 24 hours at D 49 after the inclusion. The response to the treatment will be evaluated during the inclusion visit (V1/D0) and after 6 weeks of treatment, during the following visit (V3/D49). The level of the global pain of the patient during the last 24 hours will be collected by investigators with a VAS (0 mm = no pain ; 100mm = maximun pain) at each visit.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
67
Rebel Reliever knee brace + usual antalgic treatment + physical exercises recommendations
Usual antalgic treatment + physical exercises recommendations
Euraxi Pharma
Joué-lès-Tours, Bp 80325, France
Evolution of the last 24 hours knee pain (VAS)
Time frame: Between Day 49 and Day 0
Evolution of knee pain on movement (VAS)
Evaluation with Visual Analysis Scale
Time frame: Between Day 49 and Day 0
Evolution of Lequesne Algofunctional index score
Time frame: Between D49 and Day 0
Responder rate according to OARSI-OMERACT criteria
Time frame: At Day 49
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