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首页> 外文期刊>Arzneimittel-Forschung: =Drug Research >Efficacy and safety of an oral formulation of cetirizine and prolonged-release pseudoephedrine versus xylometazoline nasal spray in nasal congestion.
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Efficacy and safety of an oral formulation of cetirizine and prolonged-release pseudoephedrine versus xylometazoline nasal spray in nasal congestion.

机译:西替利嗪和缓释伪麻黄碱与木洛他唑鼻喷剂口服制剂在鼻充血中的疗效和安全性。

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The aim of this study was to compare the decongestant properties and tolerability of the sympathomimetic xylometazoline hydrochloride 0.1% (CAS 1218-35-5, XMZ) and an oral formulation of cetirizine hydrochloride 5 mg and pseudoephedrine hydrochloride 120 mg (CAS 83881-51-0 and 90-82-4, CTZ/PSE; Cirrus). Thirty-six asymptomatic patients suffering from perennial allergic rhinitis from house dust mite were randomized to this open two-period crossover study. Patients received the study medications for four days each. In each period, treatments were taken twice a day. On day 1 in each period, immediately after the first dose of medication, patients were challenged with Dermatophagoides pteronyssinus extract 1 in the Vienna Challenge Chamber for 5 h. Primary efficacy parameters were nasal congestion evaluated by digital analysis of nasal cavity photographs and nasal airflow. Furthermore amounts of nasal secretions, nasal and ocular symptoms were recorded. In addition, 5 independent Ear-Nose-Throat specialists also assessed nasal cavity photographs. Statistical analyses were conducted at the 5% level of significance. Digital analysis of the nasal cavity photographs as well as nasal airflow measurements did not differentiate XMZ from CTZ/PSE. Ratings of the photographs of the nasal cavity emphasized the rapid onset of XMZ. No clinically relevant adverse events were recorded. This rapid onset of action but short-lived effect of topical xylometazoline 0.1% should be balanced against the consistent and prolonged effect of systemic cetirizine/pseudoephedrine combination in the treatment of perennial allergic rhinitis as no significant differences between these 2 medications were noted regarding their decongestant properties. With the exception of nasal obstruction, all subjective symptoms as well as the global condition were significantly better under CTZ/PSE. Amounts of nasal secretions during these sessions were significantly lower with CTZ/PSE.
机译:这项研究的目的是比较拟交感神经药盐酸咯米唑啉0.1%(CAS 1218-35-5,XMZ)和盐酸西替利嗪5 mg和盐酸伪麻黄碱120 mg的口服制剂(CAS 83881-51-)的去充血性能和耐受性0和90-82-4,CTZ / PSE; Cirrus)。将36例因屋尘螨而患的常年性变应性鼻炎的无症状患者随机分配至这项开放式的两期交叉研究。患者接受为期四天的研究药物。在每个时期,每天进行两次治疗。在每个阶段的第1天,在首次服药后,立即在维也纳挑战室对患者进行Dermatophagoides pteronyssinus提取物1攻击5小时。主要功效参数是通过对鼻腔照片和鼻气流的数字分析来评估鼻充血。此外,记录鼻分泌物,鼻和眼症状的量。此外,还有5位独立的耳鼻喉专家对鼻腔照片进行了评估。统计分析以5%的显着性水平进行。鼻腔照片的数字分析以及鼻气流测量结果并未将XMZ与CTZ / PSE区分开。鼻腔照片的评分强调了XMZ的快速发作。没有临床相关不良事件的记录。这种快速起效但局部用药0.1%的甲氧咪唑啉的短期作用应与全身性西替利嗪/伪麻黄碱联合治疗常年性变应性鼻炎的持续和长期作用相平衡,因为这两种药物在充血性充血方面无显着差异属性。除鼻塞外,在CTZ / PSE下,所有主观症状和整体状况均明显好转。使用CTZ / PSE时,这些时段的鼻腔分泌物数量明显减少。

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