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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Investigate the Effects of Kamishoyosan, a Traditional Japanese Medicine, on Menopausal Symptoms: The KOSMOS Study
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A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Investigate the Effects of Kamishoyosan, a Traditional Japanese Medicine, on Menopausal Symptoms: The KOSMOS Study

机译:多中心,随机,双盲,安慰剂对照试验,用于调查Kamishoyosan,传统日本医学,对更年期症状的影响:科斯莫斯研究

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Objective . The KOSMOS study, a multicenter, randomized, double-blind, placebo-controlled trial, investigated the effects and safety of kamishoyosan (TJ-24), a traditional Japanese medicine, in the treatment of climacteric disorder. Methods . Japanese women with climacteric disorder were administered a placebo during a 4-week run-in period, after which they were classified as placebo responders (R group) if their score on the modified Questionnaire for the Assessment of Climacteric Symptoms in Japanese Women (m-QACS) with excitability and irritability as the primary outcome improved by?≥?3 points and as placebo nonresponders (NR group) otherwise. Members of the NR group were randomly allocated to receive either TJ-24 or placebo. After 12 weeks, their m-QACS scores, anxiety and depression, sleep, and overall quality of life (QOL) were compared. Results . The TJ-24 and placebo arms in the NR group included 20 patients each. The change in the m-QACS scores of members of the NR group for excitability and irritability at 12 weeks versus baseline was –3.1?±?1.7 in the TJ-24 arm, a significant decrease, but compared with –2.7?±?2.2 in the placebo arm, no significant difference was between two arms. However, the proportion of participants whose score improved by ≥3 points was significantly higher in the TJ-24 arm. In the subgroup analysis of premenopausal women, the changes in the score for excitability and irritability were significantly larger in the TJ-24 arm. The incidence of adverse drug reactions or adverse events did not differ between the two arms, and no serious events were reported. Conclusion . Although no significant difference was identified for the primary outcome, a significantly higher proportion of patients who received TJ-24 displayed improvement. Its high level of safety and effects on excitability and irritability in premenopausal women suggest that TJ-24 may be a useful treatment.
机译:客观的 。科斯莫斯研究,多中心,随机,双盲,安慰剂对照试验,研究了甘山炎(TJ-24),传统日本医学的效果和安全性,治疗更年期疾病。方法 。在4周的运行期间,在一个4周的运行期间进行了日本妇女,之后他们被归类为安慰剂响应者(R组),如果他们在改进调查问卷上进行评估,以评估日本女性的更年期症状(M- QACS)具有兴奋性和烦躁,因为否则主要结果改善,否则是安慰剂无应答者(NR组)。随机分配NR组的成员以接收TJ-24或安慰剂。 12周后,比较了他们的M-QACS分数,焦虑和抑郁,睡眠和整体生活质量(QOL)。结果 。 NR组的TJ-24和安慰剂臂包括20名患者。 NR组的M-QACS分数的变化对于兴奋性和烦躁为12周,与基线为-3.1?±1.7在TJ-24臂中,显着降低,但与-2.7?±2.2相比在安慰剂臂中,两臂之间没有显着差异。然而,TJ-24 ARM中,参与者的比例≥3点的比例显着高。在前辈妇女的亚组分析中,TJ-24臂的兴奋性和烦躁分数的变化显着较大。两臂之间不良药物反应或不良事件的发病率没有差异,并且没有报告严重事件。结论 。虽然没有针对主要结果确定显着差异,但接受TJ-24显示改善的患者比例明显高。其高水平的安全性和对兴奋性和烦躁的影响以及前辈妇女的烦躁表明TJ-24可能是一个有用的治疗方法。

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