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The efficacy of QingfengGanke granule in treating postinfectious cough in pathogenic wind invading lungs syndrome: a multicenter, randomized, double-blind, placebo-controlled trial

机译:清风甘克颗粒治疗致病性风侵肺综合征的感染后咳嗽的功效:一项多中心,随机,双盲,安慰剂对照试验

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Background Postinfectious cough (PIC) significantly affects cough-related quality of life but still lacks effective treatments. This study aims to investigate the efficacy of QingfengGanke granule (QFGKG) in treating PIC induced by pathogenic wind invading lungs syndrome. Methods A multicenter, randomized, double-blind, placebo-controlled clinical trial was conducted. A total of 180 eligible participants were randomly (1:1:1) assigned to group A (QFGKG 6?g plus QFGKG-matched placebo 6?g), group B (QFGKG 12?g), and group C (QFGKG-matched placebo 12?g). All herbal medications were orally administered twice daily for 10 consecutive days. The primary outcome was time to cough resolution, and secondary outcomes included time to cough alleviation, mean changes in cough symptom score (CSS), visual analogue scale (VAS) score, cough-specific quality of life questionnaire (CQLQ) score, and traditional Chinese medicine (TCM) syndrome score from baseline to Day 10, as well as adverse events. Results A total of 173 participants were included in the efficacy and safety analyses (group A, n?=?57; group B, n?=?57; group C, n?=?59). The median time to cough resolution in groups A, B, and C was more than 10?days, 8?days, and more than 10?days, respectively (P?P?P?=?0.0005, P?P?=?0.0002, P?P?=?0.0258, P?=?0.0003, respectively), and TCM syndrome (P?=?0.0031, P?P?=?0.0091). The adverse event profiles were comparable among the three groups. Conclusion QingfengGanke granule is efficacious in the treatment of PIC induced by pathogenic wind invading lungs syndrome.
机译:背景感染后咳嗽(PIC)会严重影响与咳嗽相关的生活质量,但仍缺乏有效的治疗方法。本研究旨在探讨清风甘克颗粒(QFGKG)治疗病原性风侵肺综合症所致PIC的疗效。方法进行了一项多中心,随机,双盲,安慰剂对照的临床试验。总共180名合格参与者(1:1:1)被随机分为A组(QFGKG 6?g加QFGKG匹配的安慰剂6?g),B组(QFGKG 12?g)和C组(QFGKG匹配安慰剂12克)。所有草药连续10天每天口服两次。主要结局是缓解咳嗽的时间,次要结局包括缓解咳嗽的时间,咳嗽症状评分(CSS),视觉模拟量表(VAS)评分,特定于咳嗽的生活质量问卷(CQLQ)评分和传统从基线到第10天的中医(TCM)综合征评分以及不良事件。结果有效性和安全性分析共包括173名参与者(A组,n == 57; B组,n == 57; C组,n == 59)。 A,B和C组中止咳的中位时间分别超过10天,8天和10天以上(PPP?P?= 0.0005,P?P?=?。分别为0.0002,P 2 P 3 = 0.0258,P 2 = 0.0003)和中医综合症(P 2 = 0.0031,P 2 P = 0.0091)。不良事件概况在三组之间具有可比性。结论清风感咳颗粒对病原性风侵肺综合症所致的PIC治疗效果良好。

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