Dietary Supplement for Joint: the OLE Study

Exclusion Criteria

• •Related to knee
• •Recent trauma (\< 1 month) of the knee responsible of the symptomatic knee
• •Subject with knee/joint surgery/replacement and ACL (Cross Ligament) injury in the target knee
• •Concurrent articular disease interfering with the evaluation of pain such as articular dysplasia, aseptic osteonecrosis, acromegaly, Paget's disease, hemophilia, hemochromatosis, chondromatosis, villonodular synovitis of the knee, seronegative spondyloarthropathy, rheumatoid arthritis, gouty arthritis , infectious arthritis, radiculalgia in the lower limbs, arteritis
• •Prosthesis in the target knee
• •Diagnosed arthrosis eligible to knee/joint surgery/replacement
• •Related to treatments
• •Analgesics to manage knee pain 24h before inclusion visit
• •Corticosteroids injection in the target knee in the month preceding inclusion
• •Hyaluronan injection in the target knee in the last 6 months
• •Oral corticotherapy ≥ 5mg/day in the last 3 months
• •Symptomatic slow-acting drugs (SYSADs) treatment (Chondroitin, diacerein, glucosamine, soy and avocado unsaponifiables) in the last 3 months
• •Other dietary supplements used for articular disorders in the last 3 months
• •An anticipated need for the duration of the trial of corticosteroids or hyaluronan injection, oral corticotherapy, arthroscopy, analgesics other than listed as rescue treatments, which are forbidden during the trial
• •Arthroscopy in the last 6 months
• •Allergy or contra-indication to Oleuropein, to maltodextrin or any ingredient present in the product, or intolerance to rescue treatment (Paracetamol and NSAIDs)
• •Treatments based on strontium ranelate, bisphosphonates, selective estrogen-receptor modulator (SERM) and parathormone (PTH) during the year before inclusion
• •Related to associated diseases
• •Severe and uncontrolled diseases (liver or renal failure, lung/heart severe disease, Parkinson, progressive malignant neoplasia or in remission for less than 5 years, HIV, etc.)
• •Lower or upper extremity surgery or fracture in the last 3 months
• •Anticipated need for any surgical or other invasive procedure during the trial including prosthesis in the target knee
• •Swallowing disorder
• •Related to patients
• •Close collaborators to the investigational team, the study coordinator (Artialis) or to the Sponsor (Nestlé)
• •Currently participating or having participated in another therapeutic clinical trial in the three previous months
• •Having made a blood donation in the past month
• •Under guardianship or judicial protection
• •Pregnancy, breastfeeding, planned conception
• •Premenopausal women or women without tubal ligation or contraception.