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Sanfu herbal patch applied at acupoints in patients with bronchial asthma: study protocol for a randomized controlled trial

机译:Sanfu草药补丁在支气管哮喘患者的穴位应用于穴位:用于随机对照试验的研究方案

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BACKGROUND:Bronchial asthma is one of the most common inflammatory airway disorders. As one of the main non-drug therapies, the Sanfu herbal patch (SHP) has been widely used to treat bronchial asthma, although the evidence for its efficacy and associated mechanism are inconclusive. The objective of this trial is to clarify the clinical efficacy and safety of the SHP in the treatment of bronchial asthma in the chronic persistent or clinical remission stage and to provide high-quality data for further research.METHODS:We propose a multicentre, double-blinded, parallel, randomized, placebo-controlled clinical trial involving 4 study hospitals in China. A total of 72 eligible participants will be randomized into an SHP group and a placebo group. They will receive an SHP for 3 treatment sessions. The primary outcome will be changes in forced expiratory volume in 1?s after 3 treatment sessions. Secondary outcomes will include the following: (1) the Asthma Quality of Life Questionnaire, Asthma Control Test, and Asthma Long-term Follow-up Scale; (2) levels of Metallothionein-2 and Transgelin-2 in blood and urine; and (3) levels of IL-5, IL-13, IL-23, IL-25, and thymic stromal lymphopoietin in blood. Analysis of the data will be performed at baseline, at the end of the 2nd and 3rd treatment sessions, and at the 24-week follow-up. The safety of the SHP will be evaluated at each treatment session.DISCUSSION:The aims of this trial are to determine whether the SHP is more effective than placebo in the treatment of patients with bronchial asthma, as well as whether the SHP works by reducing airway inflammation and reversing bronchoconstriction.TRIAL REGISTRATION:Chinese Clinical Trial Registry ( http://www.chictr.org.cn ), ChiCTR1900024616. Registered on 19 July 2019.
机译:背景:支气管哮喘是最常见的炎症气道疾病之一。作为主要的非药物疗法之一,Sanfu草药贴剂(SHP)已被广泛用于治疗支气管哮喘,尽管其疗效和相关机制的证据是不确定的。该试验的目的是阐明SHP在慢性持续或临床缓解阶段治疗支气管哮喘的临床疗效和安全性,并为进一步研究提供高质量的数据。方法:我们提出了一种多中心,双重涉及中国4学习医院的盲目,平行,随机,安慰剂控制的临床试验。共有72名符合条件的参与者将被随机分为SHP集团和安慰剂集团。他们将收到3个治疗课程的SHP。在3次治疗会议后,主要结果将在1?s中的强制呼气量变化。二次结果将包括以下内容:(1)哮喘质量调查问卷,哮喘控制试验和哮喘长期随访规模; (2)血液和尿液中金属硫蛋白-2和Transgelin-2水平; (3)血液中IL-5,IL-13,IL-23,IL-25和胸腺基质淋巴二蛋白的水平。数据分析将在第2次和第三种治疗课程结束时在基线进行,并在24周的随访中进行。 SHP的安全将在每个治疗会议上进行评估。探讨:该试验的目的是确定SHP是否比安慰剂更有效,以治疗支气管哮喘患者,以及SHP是否通过减少气道工作炎症和逆转支气管电气.TRIAL注册:中国临床试验登记处(http://www.chictr.org.cn),CHICTR1900024616。 2019年7月19日注册。

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