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Randomized, double-blind, placebo-controlled superiority trial of the Yiqigubiao pill for the treatment of patients with chronic obstructive pulmonary disease at a stable stage

机译:益气固表丸用于稳定期慢性阻塞性肺疾病患者的随机,双盲,安慰剂对照优势试验

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In traditional Chinese medicine (TCM), the Yiqigubiao pill is commonly used to enhance physical fitness. The current clinical trial was designed to evaluate the efficacy and safety of the Yiqigubiao pill as an adjuvant therapy for patients with stable chronic obstructive pulmonary disease (COPD). The current trial was a randomized, double-blind, placebo-controlled superiority trial. The participants were recruited from outpatients at the Traditional Chinese Medicine Hospital affiliated with Xinjiang Medical University (urumqi, China) between February and September 2012. All participants were patients with stable COPD that were randomized to the Yiqigubiao pill (YQGB; n=84) or placebo (Pb; n=87) groups. The occurrences of acute exacerbation (AE) of COPD during the trial were recorded. Lung function value assessments, scoring of life quality and exercise endurance, arterial blood gas analysis and serum inflammatory cytokines level determination were performed prior to and throughout the study. A total of 139 participants completed the intervention and 132 participants completed the study. The interval between the initial intervention and the first AECOPD was greater in the YQGB group compared with the Pb group (P<0.01). The incidence rate of AECOPD was lower in the YQGB group than in the Pb group (P<0.01). Subsequent to the intervention or at the end of the study, the 6-min walking distance difference was longer in the YQGB group compared with the Pb group (P<0.01). The scores reflecting life quality decline became lower in the YQGB group (P<0.01). The serum levels of proinflammatory factors were downregulated to a greater extent in the YQGB group compared with the Pb group. Thus, the Yiqigubiao pill is an efficient and safe adjuvant therapy for the treatment of stable patients with COPD.
机译:在中药(TCM)中,益气固表丸通常用于增强体质。当前的临床试验旨在评估益气固表丸作为稳定型慢性阻塞性肺疾病(COPD)患者辅助治疗的疗效和安全性。目前的试验是一项随机,双盲,安慰剂对照的优势试验。参与者是从2012年2月至2012年9月在新疆医科大学附属中医医院门诊招募的。所有参与者均为COPD稳定的患者,随机分组服用益气固表药(YQGB; n = 84)或安慰剂(Pb; n = 87)组。记录试验期间COPD急性加重(AE)的发生。在整个研究之前和整个研究过程中,进行了肺功能值评估,生活质量和运动耐力的评分,动脉血气分析和血清炎性细胞因子水平测定。共有139位参与者完成了干预,有132位参与者完成了研究。与Pb组相比,YQGB组的初始干预与首次AECOPD之间的间隔更大(P <0.01)。 YQGB组AECOPD的发生率低于Pb组(P <0.01)。干预后或研究结束时,与Pb组相比,YQGB组的6分钟步行距离差异更大(P <0.01)。 YQGB组反映生活质量下降的得分降低(P <0.01)。与Pb组相比,YQGB组的促炎因子血清水平下调幅度更大。因此,益气固表丸是治疗稳定型COPD患者的一种安全有效的辅助疗法。

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