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首页> 外文期刊>Trials >Efficacy and safety of Qi-Wei-Qing-Yan aerosol in treatment of acute pharyngitis (lung-stomach excess-heat syndrome): study protocol for a randomized controlled trial
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Efficacy and safety of Qi-Wei-Qing-Yan aerosol in treatment of acute pharyngitis (lung-stomach excess-heat syndrome): study protocol for a randomized controlled trial

机译:七味清炎气雾剂治疗急性咽炎(肺胃过热综合征)的疗效和安全性:一项随机对照试验的研究方案

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摘要

Acute pharyngitis accounts for an estimated 15 million patient visits in the United States. However, there is no proven effective and safe treatment. Although Chinese herbal medicine is widely used in the treatment of acute pharyngitis, there is a lack of evidence-based data. Despite several clinical trials conducted in this setting, no randomized placebo-controlled trial has been performed to date. This trial aims to investigate the efficacy and safety of Qi-Wei-Qing-Yan aerosol (QWQYA), a Chinese herbal prescription, compared with a placebo aerosol in the treatment of acute pharyngitis with lung-stomach excess-heat syndrome. This is a prospective, multicenter, randomized, double-blinded, parallel-group, placebo-controlled trial. A total of 420 adult patients, of either sex, with acute pharyngitis will be enrolled from seven study sites across China. All patients will be randomly allocated to one of three parallel treatment groups: (1) QWQYA with the current propellant, (2) QWQYA with a previous propellant, and (3) the placebo aerosol with the current propellant. The study medication will be administered into the pharyngeal region in three sprays thrice daily for 5 consecutive days. The primary outcome measures are time to complete resolution of sore throat and relief rate of sore throat. Secondary outcome measures include resolution rate of sore throat, time to relief of sore throat, intensity of sore throat, and change of traditional Chinese medicine syndrome score and clinical signs score from baseline to post-treatment, as well as the occurrence of any adverse events. This will be the first clinical trial to investigate the efficacy and safety of QWQYA in the treatment of acute pharyngitis in an adult population in a multicenter, randomized, double-blinded, parallel-group, placebo-controlled manner. Not only might it establish the basis for the efficacy and safety of QWQYA in treating acute pharyngitis, but it might also provide evidence to support the use of Chinese herbal medicine in treating acute pharyngitis and thus support an alternative treatment option for management of acute pharyngitis. Chinese Clinical Trial Registry ChiCTR-IPR-15005991 .
机译:在美国,急性咽炎约占1500万人次。但是,尚无有效有效的治疗方法。尽管中草药被广泛用于治疗急性咽炎,但缺乏循证数据。尽管在这种情况下进行了多项临床试验,但迄今为止尚未进行过随机安慰剂对照试验。该试验旨在研究中草药处方味胃清炎气雾剂(QWQYA)与安慰剂气雾剂在治疗伴有肺胃过热综合征的急性咽炎中的有效性和安全性。这是一项前瞻性,多中心,随机,双盲,平行组,安慰剂对照试验。来自中国七个研究地点的总共420名成年患者,不论性别,均患有急性咽炎。所有患者将被随机分配到三个平行治疗组之一:(1)使用当前推进剂的QWQYA,(2)使用先前推进剂的QWQYA,以及(3)使用当前推进剂的安慰剂气雾剂。研究药物将连续三天每天三次三次喷入咽部区域。主要的结局指标是完成咽痛缓解和咽痛缓解率的时间。次要结果指标包括咽痛的缓解率,咽痛的缓解时间,咽痛的强度以及从基线到治疗后中医证候评分和临床体征评分的变化,以及是否发生任何不良事件。这将是第一个以多中心,随机,双盲,平行组,安慰剂对照的方式研究QWQYA治疗成人人群急性咽炎的疗效和安全性的临床试验。它不仅可以为QWQYA治疗急性咽炎的有效性和安全性奠定基础,而且还可以提供证据支持中草药治疗急性咽炎,从而为急性咽炎的治疗提供另一种治疗选择。中国临床试验注册中心ChiCTR-IPR-15005991。

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