4.3 Article

Efficacy and safety of oral strontium ranelate for the treatment of knee osteoarthritis: rationale and design of randomised, double-blind, placebo-controlled trial

Journal

CURRENT MEDICAL RESEARCH AND OPINION
Volume 28, Issue 2, Pages 231-239

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1185/03007995.2011.648758

Keywords

DMOAD; Joint space width; Knee osteoarthritis; Knee radiograph; Randomized clinical trial; Strontium ranelate; Structure-modifying treatment

Funding

  1. Servier, France
  2. Executive Committee
  3. Amgen
  4. ABBH
  5. Novartis
  6. Pfizer
  7. Eli Lilly
  8. Servier
  9. Negma
  10. Lilly
  11. Wyeth
  12. GlaxoSmithKline
  13. Roche
  14. Merckle
  15. Nycomed
  16. NPS
  17. Theramex
  18. UCB
  19. Rottapharm
  20. IBSA
  21. Genevrier
  22. Teijin
  23. Teva
  24. Ebewee Pharma
  25. Zodiac
  26. Analis
  27. Novo-Nordisk
  28. Bristol Myers Squibb
  29. Merck
  30. Novo Nordisk
  31. Groupe Fournier
  32. Proctor and Gamble
  33. Besins EscoVesco
  34. Merck Sharp and Dohme
  35. Chiesi
  36. Boehringer Mannheim
  37. Genentech
  38. ONO
  39. Abbott
  40. Janssen
  41. Merck-Schering
  42. Warner Chilcott
  43. Fidia
  44. Pierre Fabre
  45. Smith Nephews
  46. Expanscience
  47. Genzyme
  48. Medical Research Council [MC_UP_A620_1014, U1475000001] Funding Source: researchfish
  49. National Institute for Health Research [NF-SI-0508-10082] Funding Source: researchfish

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Objective: The osteoporosis drug strontium ranelate dissociates bone remodelling processes. It also inhibits subchondral bone resorption and stimulates cartilage matrix formation in vitro. Exploratory studies in the osteoporosis trials report that strontium ranelate reduces biomarkers of cartilage degradation, and attenuates the progression and clinical symptoms of spinal osteoarthritis, suggesting symptom-and structure-modifying activity in osteoarthritis. We describe the rationale and design of a randomised trial evaluating the efficacy and safety of strontium ranelate in knee osteoarthritis. Research design, methods, and results: This double-blind, placebo-controlled trial (98 centres, 18 countries) includes ambulatory Caucasian men and women aged >= 50 years with primary knee osteoarthritis of the medial tibiofemoral compartment (Kellgren and Lawrence grade 2 or 3), joint space width (JSW) 2.5 to 5 mm, and knee pain on most days in the previous month (intensity >= 40mm on a visual analogue scale). Patients are randomly allocated to three groups (strontium ranelate 1 or 2 g/day, or placebo). Follow-up is expected to last 3 years. The primary endpoint is radiographic change in JSW from baseline in each group versus placebo. The main clinical secondary endpoint is WOMAC score at the knee. Safety is assessed at every visit. It is estimated that 1600 patients are required to establish statistical significance with power >90% (0.2mm +/- 10% between-group difference in change in JSW over 3 years). Recruitment started in April 2006. The results are expected in spring 2012. Clinical trial registration: The trial is registered on www.controlled-trials.com (number ISRCTN41323372). Conclusions: This randomised, double blind, placebo-controlled study will establish the potential of strontium ranelate in improving structure and symptoms in patients with knee osteoarthritis.

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