Analgesic efficacy of a lecithin-vehiculated diclofenac epolamine gel in shoulder periarthritis and lateral epicondylitis: a placebo-controlled, multicenter, randomized, double-blind clinical trial.

G Spacca, A Cacchio, A Forgács, P Monteforte, G Rovetta
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Abstract

Diclofenac epolamine (2-hydroxyethyl-pyrrolidine) (DHEP) is a diclofenac salt endowed with enhanced cutaneous permeation. To optimize its absorption after topical application, a lecithin-enriched DHEP 1.3% gel has been developed (DHEP lecithin gel) and investigated in patients with shoulder periarthritis and lateral epicondylitis in a placebo-controlled, multicenter double-blind clinical trial. One hundred fifty-eight patients were randomized to a 10-day treatment with DHEP lecithin gel or placebo (5 g t.i.d. applied on the painful area). The efficacy criteria were pain measured by visual analog scale (VAS) while performing a specific standardized movement, intake of rescue medication (paracetamol), and the disabilities of the arm, shoulder and hand (DASH) questionnaire. VAS scores indicated a consistently higher analgesic activity of DHEP lecithin gel. At day 3, pain was reduced by -20.1 +/- 20.2 and -9.9 +/- 12.7 mm in the DHEP lecithin gel- and placebo-treated patients, respectively (p < 0.001); at day 6 of treatment, DHEP lecithin gel induced a pain reduction of -33.2 +/- 26.1 mm, while the reduction achieved with placebo was only -21.2 +/- 18.8 mm (p < 0.001). The mean changes in DASH questionnaire indicated that DHEP lecithin gel was more effective than placebo in improving patient well-being and reducing difficulties in performing the activities most severely impaired by rheumatism, while no difference was observed between the two treatments in consumption of rescue medication. In conclusion, these results indicate that DHEP lecithin gel is a topically effective analgesic product in patients with shoulder periarthritis or lateral epicondylitis and provide further evidence on the use of topical nonsteroidal anti-inflammatory drugs as an optimal approach to the treatment of localized musculoskeletal disorders.

卵磷脂载药双氯芬酸依泊胺凝胶治疗肩周炎和外侧上髁炎的镇痛效果:一项安慰剂对照、多中心、随机、双盲临床试验
双氯芬酸乙polamine(2-羟乙基吡咯烷)(DHEP)是一种双氯芬酸盐,具有增强皮肤渗透性。为了优化外用后的吸收效果,我们研制了一种富含卵磷脂的脱氢磷1.3%凝胶(脱氢磷卵磷脂凝胶),并通过安慰剂对照、多中心双盲临床试验对肩周炎和外上髁炎患者进行了研究。158名患者随机接受DHEP卵磷脂凝胶或安慰剂治疗10天(每次5克,涂抹在疼痛部位)。疗效评价标准为:采用视觉模拟量表(VAS)测量特定标准化运动时的疼痛程度、对乙酰氨基酚(paracetamol)的服用情况、手臂、肩膀和手的残疾程度(DASH)问卷。VAS评分显示DHEP卵磷脂凝胶具有较高的镇痛活性。在第3天,DHEP卵磷脂凝胶组和安慰剂组的疼痛分别减少了-20.1 +/- 20.2和-9.9 +/- 12.7 mm (p < 0.001);在治疗第6天,DHEP卵磷脂凝胶诱导疼痛减轻-33.2 +/- 26.1 mm,而安慰剂的减少仅为-21.2 +/- 18.8 mm (p < 0.001)。DASH问卷的平均变化表明,DHEP卵磷脂凝胶在改善患者幸福感和减少风湿病最严重损害的活动困难方面比安慰剂更有效,而两种治疗在抢救药物的消耗方面没有差异。综上所述,这些结果表明DHEP卵磷脂凝胶是肩周炎或外上髁炎患者的局部有效镇痛产品,并进一步证明外用非甾体类抗炎药是治疗局部肌肉骨骼疾病的最佳方法。
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