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首页> 外文期刊>Progress in Artificial Intelligence >A Randomized, Double-Blind, Placebo-Controlled Trial of Ibuprofen Lysinate in Comparison to Ibuprofen Acid for Acute Postoperative Dental Pain
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A Randomized, Double-Blind, Placebo-Controlled Trial of Ibuprofen Lysinate in Comparison to Ibuprofen Acid for Acute Postoperative Dental Pain

机译:与布洛芬酸急性术后牙痛相比,布洛芬溶解的随机,双盲,安慰剂对照试验相比之下

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Introduction Ibuprofen acid is poorly soluble in the stomach, thus reaching maximum plasma levels at approximately 90 min post-dose. Ibuprofen lysinate has been developed to accelerate absorption of ibuprofen to shorten the time to analgesic efficacy. This study compared analgesic efficacy and onset of effect of a single dose of ibuprofen lysinate or ibuprofen acid in patients undergoing third molar extraction. Methods Randomized, double-blind, placebo-controlled, multi-center, parallel-group single-dose study. Adults (18-60 years) undergoing extraction of >= 1 third molar were randomized 2:2:1 to ibuprofen lysinate, ibuprofen acid, or placebo postoperatively. Pain relief (PAR, 5-point scale, 0 = none to 4 = complete pain relief) and pain intensity (PI, 100 mm visual analog scale) were assessed between 15 and 360 min post-dose. The primary endpoint was the weighted sum of PAR scores at 6 h (TOTPAR). Time to onset of effect, global assessment of efficacy, and adverse events were also assessed. Results Overall, 351 patients received ibuprofen lysinate (N = 141), ibuprofen acid (N = 139), or placebo (N = 71). Both active treatments significantly reduced pain compared with placebo, from 15 min post-dose to 6 h (TOTPAR: ibuprofen lysinate: 19.57; ibuprofen acid: 19.96; placebo: 8.27). Ibuprofen lysinate was significantly more effective than placebo, but non-inferior to ibuprofen acid, at providing pain relief over 6 h. There was no significant difference between ibuprofen lysinate and ibuprofen acid for onset of analgesia. Both ibuprofen formulations were well tolerated; all adverse events were mild to moderate and considered unrelated to treatment. Conclusions A single dose of ibuprofen lysinate is non-inferior to ibuprofen acid in terms of analgesic efficacy, onset of action, and tolerability in patients who have recently undergone dental surgery. Plain Language Summary Plain language summary available for this article.
机译:引言布洛芬酸在胃中溶于差,从而在剂量后约90分钟达到最大血浆水平。已经开发了布洛芬溶解苷,以加速布洛芬的吸收,以缩短镇痛效果的时间。该研究比较了第三摩尔萃取患者的镇痛效果和单剂量布洛芬溶酶或布洛芬酸的效果。方法随机,双盲,安慰剂控制,多中心,并联单剂量研究。在术后2:2:1术后,成年人(18-60岁)接受促进> = 1三分之一的溶液,是布洛芬酸酯,布洛芬酸或安慰剂。疼痛缓解(PAR,5分,0 = 4 =完全疼痛缓解)和疼痛强度(PI,100 mm视觉模拟量表)在15-360分钟的剂量后评估。主要终点是6小时(TotPAR)的PAR分数的加权和。还评估了效果,全局评估和不良事件的效果的时间。结果总体而言,351名患者接受布洛芬溶液(n = 141),布洛芬酸(n = 139),或安慰剂(n = 71)。与安慰剂相比,与安慰剂相比,疼痛显着降低了疼痛显着减少至6小时(Totpar:布洛芬溶解素:19.57;布洛芬酸:19.96;安慰剂:8.27)。布洛芬裂解肽比安慰剂更有效,但不逊于布洛芬酸,在6小时内提供疼痛缓解。布洛芬溶解素和布洛芬酸对镇痛发病的情况无显着差异。布洛芬配方均良好耐受;所有不良事件均为温和,适度和治疗无关。结论单剂量的布洛芬溶解素在镇痛疗效,发作和最近经历牙科手术的患者的患者发作和耐受性方面是非较差的。纯语言摘要纯语言摘要可用于本文。

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