Osteoarthritis Musculoskeletal Diseases Arthrosis
Conditions
Interventions
Strontium ranelate versus placebo.
Sponsors
Institut de Recherches Internationales Servier (France)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Caucasian males or females 2. Aged 45 years or over 3. Primary knee osteoarthritis 4. Under an effective contraceptive method for non-menopausal women
Exclusion criteria
Exclusion criteria: 1. Knee prosthesis already implanted, or foreseen to be implanted 2. Hip prosthesis already implanted or not well-tolerated or foreseen to be implanted 3. Previous osteotomy on the inferior limbs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the algofunctional behaviour of the target knee. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Algofunctional assessment 2. Radiographic assessment of knee osteoarthritis 3. Physical examination | — |
Countries
Belgium
Outcome results
None listed