首页> 外文期刊>Pilot and Feasibility Studies >HATRIC: a study of Pelargonium sidoides root extract EPs7630 (Kaloba) for the treatment of acute cough due to lower respiratory tract infection in adultsstudy protocol for a double blind, placebo-controlled randomised feasibility trial
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HATRIC: a study of Pelargonium sidoides root extract EPs7630 (Kaloba) for the treatment of acute cough due to lower respiratory tract infection in adultsstudy protocol for a double blind, placebo-controlled randomised feasibility trial

机译:HATRIC:天竺葵根提取物EPs7630(Kaloba)用于治疗成人下呼吸道感染引起的急性咳嗽的研究双盲,安慰剂对照的随机可行性试验方案

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BackgroundAcute lower respiratory tract infection is a common acute infection managed in primary care. The current dominant management strategy in the UK is antibiotics, despite widespread publicity regarding antimicrobial resistance and evidence that the small benefits of antibiotics do not outweigh the harms. There is a need to address the rising problem of antibiotic resistance by providing credible alternative strategies, which reduce symptom burden. There is sufficient evidence to recommend the use of Pelargonium sidoides root extract in order to warrant undertaking an independent clinical trial.We propose a feasibility study to demonstrate our ability to recruit and retain patients and conduct a placebo-controlled trial of Pelargonium sidoides extract EPs?7630 in lower respiratory tract infection where pneumonia is not suspected. Both the tablet and liquid formulations will be included.MethodsThe HATRIC trial is a double-blind randomised placebo-controlled feasibility study aiming to determine the potential to conduct a fully powered trial of Pelargonium sidoides root extract as an alternative to the inappropriate use of antibiotics for acute bronchitis in UK primary care.Primary care sites will be equally randomised to one of two formulation groups (tablet or liquid preparation). Additionally, within each site, patients will be evenly randomised to active or placebo treatment. Antibiotic consumption will be monitored during the trial, but the use of a delayed prescription strategy is encouraged. The target sample size for this study is 160 patients overall or 40 per arm, recruited from approximately 20 primary care sites. The analysis will be descriptive focusing on estimation with no formal comparison of groups taking place.DiscussionIf this trial demonstrates the feasibility of recruitment and delivery, we will seek funding for a fully powered placebo-controlled trial of Pelargonium sidoides root extract for the treatment of lower respiratory tract infections in primary care.Trial registrationHATRIC was registered on the ISRCTN registry (ISRCTN17672884) on 16 August 2018.
机译:背景急性下呼吸道感染是初级保健中常见的急性感染。尽管对抗菌素耐药性的宣传广为流传,而且有证据表明抗生素的小好处并没有超过危害,但英国目前的主要管理策略是抗生素。有必要通过提供可减少症状负担的可靠替代策略来解决日益增加的抗生素耐药性问题。有足够的证据推荐使用天竺葵根提取物以确保进行独立的临床试验。我们提出一项可行性研究,以证明我们招募和挽留患者并进行天竺葵提取物在怀疑没有肺炎的下呼吸道感染中提取EPs?7630。方法HATRIC试验是一项双盲随机安慰剂对照的可行性研究,旨在确定进行完全有效的天竺葵根提取物替代不当使用的试验的潜力。英国初级保健中用于急性支气管炎的抗生素的数量。初级保健地点将被随机分配到两个制剂组(片剂或液体制剂)之一。此外,在每个部位,患者将平均随机接受积极或安慰剂治疗。在试验期间将监测抗生素的消耗,但鼓励使用延迟处方策略。该研究的目标样本量为160名患者,或每臂40名患者,从大约20个初级保健场所招募。分析将只针对估计性进行描述性分析,而无需进行正式的组别比较。讨论如果该试验证明了募集和交付的可行性,我们将寻求资助进行完全有效的安慰剂对照试验,其中包括香叶天竺葵根提取物。在初级保健中治疗下呼吸道感染的方法。临床注册HATRIC已于2018年8月16日在ISRCTN注册中心(ISRCTN17672884)注册。

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