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

机译:雷奈酸锶口服液治疗膝部骨关节炎的疗效和安全性:随机,双盲,安慰剂对照试验的原理和设计

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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 5mm, 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 2g/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.
机译:目的:骨质疏松症药物雷奈酸锶能解离骨重塑过程。它还在体外抑制软骨下骨吸收并刺激软骨基质形成。骨质疏松症试验的探索性研究报告称,雷奈酸锶可降低软骨降解的生物标志物,并减轻脊柱性骨关节炎的进展和临床症状,提示骨关节炎的症状和结构改变活性。我们描述了评估雷奈酸锶在膝骨关节炎中的疗效和安全性的随机试验的原理和设计。研究设计,方法和结果:这项双盲,安慰剂对照试验(在18个国家/地区的98个中心进行)包括年龄≥50岁,患有内侧胫股间隔原发性膝骨关节炎(Kellgren和Lawrence 2级或2级或50岁以上的非卧床白人)。 3),关节间隙宽度(JSW)为2.5至5mm,并且在前一个月的大多数日子中膝盖疼痛(在视觉模拟量表上,强度≥40mm)。将患者随机分为三组(雷奈酸锶1或2g /天,或安慰剂)。预计持续3年。主要终点是每组相对于安慰剂的JSW影像学变化。主要的临床次要终点是膝盖的WOMAC评分。每次访问都评估安全性。估计需要1600名患者来建立统计学显着性,且功效> 90%(3年内JSW变化的组间差异为0.2mm±10%)。招聘于2006年4月开始。预期结果将于2012年春季开始。临床试验注册:该试验在www.control-trials.com上注册(编号ISRCTN41323372)。结论:这项随机,双盲,安慰剂对照的研究将确定雷奈酸锶改善膝部骨关节炎患者的结构和症状的潜力。

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