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首页> 外文期刊>International journal of clinical practice >A one-year, randomised, placebo (saline) controlled clinical trial of 500-730 kDa sodium hyaluronate (Hyalgan) on the radiological change in osteoarthritis of the knee.
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A one-year, randomised, placebo (saline) controlled clinical trial of 500-730 kDa sodium hyaluronate (Hyalgan) on the radiological change in osteoarthritis of the knee.

机译:500-730 kDa透明质酸钠(Hyalgan)为期一年的随机安慰剂(盐水)对照临床试验,研究膝关节骨关节炎的放射学变化。

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The primary objective of this study was to investigate structural changes, as measured by joint space narrowing (JSN), within the knee joint during treatment with intra-articular sodium hyaluronate (HA) of molecular weight 500-730 kDa in patients with osteoarthritis (OA) of the knee. Patients received a weekly intra-articular injection of either 20 mg2/ml HA or a 2 ml vehicle placebo (saline) for three weeks. This course was repeated twice more at four-monthly intervals. Concomitant treatment with analgesics or NSAIDs was allowed. The primary efficacy measure was the reduction in mean joint space width (JSW) of the medial compartment at 52 weeks. A total of 408 patients were randomised and 319 completed the one-year study (HA: n=160, placebo: n=159); 273 of the 319 were included in the primary analysis. Analysis of variance on these 273 patients did not show a statistically significant difference between the two treatment groups. However, there was a significant difference in response to treatment in terms of the baseline JSW (p=0.01), indicating that outcome of treatment may depend on-baseline JSW. Therefore, a subgroup analysis by baseline JSW was conducted. This compared patients with a JSW >4.6 mm with those with a JSW <4.6 mm. In those with radiologically milder disease at baseline and receiving HA, the JSN was significantly reduced compared with placebo (p=0.02). In patients with radiologically more severe disease there was no difference in JSN between the two treatments. Although, in this one-year study, no overall treatment effect was seen, those with radiologically milder disease at baseline had less progression of joint space narrowing when treated with HA.
机译:这项研究的主要目的是研究在骨关节炎(OA)患者中使用分子量为500-730 kDa的关节内透明质酸钠(HA)治疗期间膝关节内的结构变化,方法是通过关节间隙变窄(JSN)进行测量)的膝盖。患者每周接受20 mg2 / ml HA或2 ml载体安慰剂(盐水)的关节内注射,持续3周。此过程每四个月间隔重复两次。允许与止痛药或非甾体抗炎药同时治疗。主要疗效指标是在52周时,减少内侧隔室的平均关节间隙宽度(JSW)。共有408位患者被随机分组​​,其中319位完成了为期一年的研究(HA:n = 160,安慰剂:n = 159); 319个分析中的273个包含在主要分析中。对这273位患者的方差分析未显示两个治疗组之间的统计学差异。但是,就基线JSW而言,对治疗的反应存在显着差异(p = 0.01),表明治疗结果可能取决于基线JSW。因此,通过基线JSW进行了亚组分析。这将JSW> 4.6 mm的患者与JSW <4.6 mm的患者进行了比较。在基线时放射学较轻且接受HA的患者,与安慰剂相比,JSN显着降低(p = 0.02)。在放射学上较严重的疾病患者中,两种治疗之间的JSN没有差异。尽管在这项为期一年的研究中,未观察到总体治疗效果,但在基线时放射学较轻的患者在接受HA治疗时关节间隙变窄的进展较少。

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