首页> 外文期刊>Arthritis & Rheumatism >Efficacy, safety, and effects on blood pressure of naproxcinod 750 mg twice daily compared with placebo and naproxen 500 mg twice daily in patients with osteoarthritis of the hip: A randomized, double-blind, parallel-group, multicenter study†
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Efficacy, safety, and effects on blood pressure of naproxcinod 750 mg twice daily compared with placebo and naproxen 500 mg twice daily in patients with osteoarthritis of the hip: A randomized, double-blind, parallel-group, multicenter study†

机译:与安慰剂和萘普生500 mg萘普生相比,髋骨关节炎患者每天两次750 mg的疗效,安全性和对血压的影响:一项随机,双盲,平行组,多中心研究†< / sup>

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ObjectiveTo test the superiority of naproxcinod compared with placebo in relieving the signs and symptoms of hip osteoarthritis and to assess the safety of naproxcinod and its effects on blood pressure.MethodsIn a 13-week, randomized, double-blind, parallel-group, multicenter study, 810 patients were randomized to receive either naproxcinod 750 mg twice daily, placebo, or naproxen 500 mg twice daily (2:2:1). Primary efficacy analyses compared naproxcinod and placebo using an analysis of covariance for 3 co-primary end points (the Western Ontario and McMaster Universities Osteoarthritis Index [WOMAC] pain and function subscales and patient's overall rating of disease status). Safety assessments included adverse events and in-office blood pressure measurements.ResultsThe least squares mean changes from baseline were significantly greater with naproxcinod than with placebo (P 0.0001) and were similar to those with naproxen at week 13 for the WOMAC pain score (−25.81, −17.97, and −24.31 mm, respectively), the WOMAC function score (−22.24, −13.45, and −21.67 mm, respectively), and patient's rating of disease status (0.86, 0.51, and 0.82, respectively). Changes from baseline in systolic blood pressure were similar in the naproxcinod and placebo groups at weeks 2, 6, and 13 (differences between groups of 0.25, −0.45, and −0.11 mm Hg, respectively). Changes in the naproxen group were greater than those in the placebo group (differences of 3.11, 3.03, and 2.00 mm Hg, respectively). Systolic blood pressure increases ≥10 mm Hg from baseline to week 13 occurred in 13.3%, 15.0%, and 20.3% of patients receiving naproxcinod, placebo, and naproxen, respectively. Naproxcinod and naproxen had similar adverse event and general safety profiles.ConclusionThe efficacy of naproxcinod for treating the signs and symptoms of hip osteoarthritis was statistically superior to that of placebo and similar to that of naproxen. Naproxcinod was well tolerated, with effects on systolic blood pressure similar to those of placebo.
机译:目的测试萘普生与安慰剂相比在缓解髋骨关节炎的体征和症状方面的优越性,并评估萘普生的安全性及其对血压的影响。方法在一个为期13周的随机,双盲,平行组,多中心研究中810名患者被随机分配接受每天两次750 mg萘普生,安慰剂或每天两次(500:2:2)的萘普生500 mg。主要功效分析使用3个主要共同终点的协方差分析(西安大略省和麦克马斯特大学骨关节炎指数[WOMAC]疼痛和功能分量表以及患者对疾病状况的总体评价)比较了萘普生和安慰剂。安全性评估包括不良事件和办公室内血压测量结果结果,萘普生与基线相比最小平方均值明显高于安慰剂组(P <0.0001),并且与WOMAC疼痛评分在第13周时与萘普生相似(− 25.81,-17.97和-24.31毫米),WOMAC功能评分(分别为-22.24,-13.45和-21.67毫米)和患者的疾病状态评分(分别为0.86、0.51和0.82)。在第2、6和13周时,萘普生和安慰剂组的收缩压相对于基线的变化相似(两组之间的差异分别为0.25,-0.45和-0.11 mm Hg)。萘普生组的变化大于安慰剂组(分别为3.11、3.03和2.00 mm Hg)。从基线到第13周,收缩压升高≥10 mm Hg的患者分别接受萘普生,安慰剂和萘普生的患者分别为13.3%,15.0%和20.3%。萘普生与不良反应和一般安全性相似。结论萘普生治疗髋部骨关节炎的体征和症状的疗效在统计学上优于安慰剂,与萘普生相似。萘普生具有良好的耐受性,对收缩压的影响与安慰剂相似。

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