首页> 美国卫生研究院文献>British Journal of Sports Medicine >Escin/diethylammonium salicylate/heparin combination gels for the topical treatment of acute impact injuries: a randomised double blind placebo controlled multicentre study
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Escin/diethylammonium salicylate/heparin combination gels for the topical treatment of acute impact injuries: a randomised double blind placebo controlled multicentre study

机译:Escin /水杨酸二乙铵/肝素联合凝胶用于局部治疗急性撞击伤:随机双盲安慰剂对照多中心研究

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摘要

>Objectives: To investigate the clinical efficacy and safety of escin-containing gels in the topical treatment of blunt impact injuries. >Methods: Competitors in soccer, handball, or karate competitions were enrolled within two hours of sustaining a strain, sprain, or contusion and treated three times with the trial gel within a period of eight hours. Patients were randomised to three parallel groups consisting of two active treatment gels, containing escin (1% or 2%), 5% diethylammonium salicylate, and 5000 IU heparin, or placebo gel. Tenderness produced by pressure was measured at 0 (baseline), 1, 2, 3, 4, 6, and 24 hours after enrolment (within two hours of the injury). Tenderness was defined as the amount of pressure (measured by a calibrated caliper at the centre of the injury) that first produced a pain reaction as reported by the patient. >Results: A total of 158 patients were enrolled; 156 were evaluated in the intention to treat analysis. The primary efficacy variable was the area under the curve for tenderness over a six hour period. The gel preparations containing 1% and 2% escin were significantly more effective (a priori ordered hypotheses testing controlling the multiple α = 5% significance level) than placebo (p1 = 0.0001 and p2 = 0.0002 respectively). The treatment effects were 5.7 kp h/cm2 (95% confidence interval (CI) 2.9 to 8.5) and 5.9 kilopond (kp) h/cm2 (95% CI 2.9 to 8.8) between 1% escin and placebo and between 2% escin and placebo respectively. These results were supported by secondary efficacy variables. The time to reach the baseline contralateral tenderness value (resolution of pain) at the injured site was shorter in the treatment groups than in the placebo group (p<0.0001). Both active gel preparations produced more rapid pain relief than the placebo gel. No relevant differences were detected between the two active gels. The safety and tolerability of the escin-containing gels were excellent. >Conclusions: Escin/diethylammonium salicylate/heparin combination gel preparations are effective and safe for the treatment of blunt impact injuries.
机译:>目的:研究含七叶皂苷凝胶在钝性撞击伤局部治疗中的临床疗效和安全性。 >方法:参加足球,手球或空手道比赛的运动员在承受拉伤,扭伤或挫伤的两个小时内入选,并在八小时内用试验凝胶进行了三次治疗。将患者随机分为三个平行组,由两个活性治疗凝胶组成,其中包含七叶红素(1%或2%),5%水杨酸二乙铵和5000 IU肝素或安慰剂凝胶。在入组后0小时(基线),1、2、3、4、6和24小时(受伤两小时内)测量压力引起的压痛。压痛被定义为首先产生患者反应的疼痛反应的压力量(通过位于受伤中心的校准卡尺测量)。 >结果:共有158名患者入选;进行了156次评估,旨在进行治疗分析。主要功效变量是六个小时内压痛曲线下的面积。含有1%和2%七叶红素的凝胶制剂比安慰剂(分别为p1 = 0.0001和p2 = 0.0002)显着更有效(先验假设假设控制多重α= 5%显着性水平)。治疗效果为5.7 kp h / cm 2 (95%置信区间(CI)2.9至8.5)和5.9千帕(hp)h / cm 2 (95%CI 2.9至8.8)分别在1%七叶素和安慰剂之间以及2%七叶素和安慰剂之间。这些结果得到次要功效变量的支持。与安慰剂组相比,治疗组在受伤部位达到基线对侧压痛值(缓解疼痛)的时间短(p <0.0001)。两种活性凝胶制剂均比安慰剂凝胶产生更快的止痛效果。在两种活性凝胶之间未检测到相关差异。含七叶皂苷凝胶的安全性和耐受性极好。 >结论: Escin /水杨酸二乙铵/肝素联合凝胶制剂可有效,安全地治疗钝性撞击伤。

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