Platelet-rich Plasma in Symptomatic Knee Osteoarthritis

Hypothesis/Objective:

The main objective of this trial is to assess the pain decrease over the last 48 hours assessed by simple numerical scale (NRS) at W14 after 3 weekly injections of PRP (W0, W1 and W2) compared to 3 injections of an equivalent volume of physiological serum in patients suffering from a knee osteoarthritis of moderate radiological severity [Kellgren and Lawrence (KL) 2 or 3].

The secondary objectives will aim to compare the decrease in the level of pain and functional assessed by NRS at W8 and W26, WOMAC scores at W8, W14 and W26, by OMERACT-OARSI response at W8, W14 and W26, in EQ5D-5L score at W8, W14 and W26 between PRN and placebo group. We will also assess the decrease in the consumption of analgesics at W8, W14 and W26 and the decrease in serum level of Coll2-1, Coll2-1 NO₂ and increase in PIIANP level at W8 and W14

Inclusion criteria

• Age between 40 and 79
• Symptomatic knee OA according to ACR criteria evolving for more than 3 months
• Predominantly femoro-tibial pain
• KL 2 or 3 on femorotibial compartment on X-rays of less than 6 months
• ENS ≥ 40/100 (with or without usual analgesic treatments)
• Failures or contraindications to conventional treatments (analgesics, NSAIDs)
• Patient able to understand the requirements of the trial and having signed a free and informed consent before entering the study
• Patient able to read and understand written instructions
• Patient able to complete the self-questionnaires
• Use of effective contraception in premenopausal women

Exclusion criteria

• Other pathologies of the lower limbs interfering with the evaluation of knee osteoarthritis (symptomatic hip OA, Lumbar pain…)
• Symptomatic contralateral knee OA with NRS ≥ 40/100
• Predominant patellofemoral symptoms
• Radiographic knee OA stage 1 or 4 of KL
• Predominant radiographic patellofemoral OA
• History of target knee surgery with material
• History of inflammatory or microcrystalline rheumatism
• History of fibromyalgia
• Morbid obesity (BMI> 40kgs / m2)
• Inflammatory flare (KOFUS score ≥ 7)
• Use of opioids in the month prior to inclusion
• Patient refusing to stop NSAIDs during the study and conventional analgesics 48 hours
• History of infection of the target knee
• Presence of chondrocalcinosis on the frontal x-ray
• Previous PRP injection
• Injection of HA or CS into the target knee during the last 3 months
• History of hemostasis disorders or taking a curative dose of anticoagulant
• Treatment with antiplatelet agents [Acetylsalicylic acid (Aspegic, Kardegic, Duoplavin, Resitune, Asasantine), Clopidogrel (Plavix, Duoplavin), Dipyridamole (Persantine, Cleridium, Asasantine)]
• Haematological disease in progress or in remission for less than 5 years (malignant hemopathies, myelodysplasia, autoimmune thrombocytopenia)
• Thrombocytopenia (<150,000 platelets)
• Patient undergoing treatment with chemotherapy or immunosuppressive drugs
• Infection at the time of inclusion (bacterial infection and / or presence of fever and / or taking antibiotics)
• Participation in a clinical trial on knee osteoarthritis during the last year
• Participation in any clinical trial completed less than 3 months ago
• Patient whose mental state does not allow him to understand the nature, objectives and possible consequences of the study
• Patient under legal protection (curatorship or guardianship)
• Pregnant woman or planning to become pregnant during the study or breastfeeding