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首页> 外文期刊>Open access Journal of Sports Medicine >Pooled analysis of clinical trial data evaluating the safety and effectiveness of diclofenac epolamine topical patch 1.3% for the treatment of acute ankle sprain
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Pooled analysis of clinical trial data evaluating the safety and effectiveness of diclofenac epolamine topical patch 1.3% for the treatment of acute ankle sprain

机译:临床试验数据汇总分析,评估双氯芬酸依泊明局部贴剂1.3%治疗急性踝关节扭伤的安全性和有效性

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Abstract: This pooled analysis assessed the efficacy and safety of the diclofenac epolamine topical patch 1.3% (DETP) for the treatment of acute mild-to-moderate ankle sprain. Data from 2 randomized, double-blind, placebo-controlled studies enrolling 274 male and female patients aged 18 to 65 years with acute ankle sprain were pooled and evaluated. The primary end point was pain reduction on movement assessed using a 100 mm visual analog scale (VAS). Safety and tolerability were also assessed. Beginning approximately 3 hours after initial treatment, DETP-treated patients experienced statistically significant and sustained lower mean VAS scores in pain intensity on movement (mean ± SD, 54.1 ± 20.0 mm versus 60.3 ± 16.8 mm) compared with placebo-treated patients, representing a 20% versus 13% reduction in VAS pain scores from baseline (P = 0.012). This statistically significant difference in mean VAS score was maintained through day 7 (9.4 ± 14.4 mm versus 18.4 ± 18.2 mm, P < 0.0001). The DETP and placebo patches were well tolerated. These results further confirm the efficacy and safety of DETP for the treatment of acute pain from ankle sprains.
机译:摘要:这项汇总分析评估了双氯芬酸依泊敏1.3%局部贴剂(DETP)治疗急性轻度至中度踝扭伤的疗效和安全性。汇总并评估2项随机,双盲,安慰剂对照研究的数据,这些研究纳入了274名年龄在18至65岁之间的急性脚踝扭伤的男性和女性患者。主要终点是使用100毫米视觉模拟评分(VAS)评估的运动减轻疼痛。还评估了安全性和耐受性。在初次治疗后约3小时开始,与安慰剂治疗的患者相比,经DETP治疗的患者在运动时的疼痛强度经历了统计学上显着且持续的平均VAS评分降低(平均±SD,54.1±20.0 mm对60.3±16.8 mm)。与基线相比,VAS疼痛评分降低了20%,而降低了13%(P = 0.012)。到第7天,VAS平均得分的这一统计显着差异得以维持(9.4±14.4 mm对18.4±18.2 mm,P <0.0001)。 DETP和安慰剂补丁的耐受性良好。这些结果进一步证实了DETP治疗脚踝扭伤引起的急性疼痛的有效性和安全性。

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