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Study of efficacy and safety of Jiaotai pill in the treatment of depression

机译:焦田丸在抑郁症治疗中的疗效和安全性研究

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Background: Depression is a common affective disorder characterized by marked and lasting melancholia, with corresponding thought and behavior changes. Due to an accelerated pace of life and increased work pressure, the incidence of depression has risen sharply, causing great harm to family and social life. Jiaotai pill (JTP) is a Chinese herbal formula that is commonly prescribed for depression and insomnia in clinical treatment, and exhibits antidepressant effects as shown in animal experimental research. However, there are no standard clinical trials to confirm its efficacy in treating depression . Objective: This study aims to assess the efficacy and safety of JTP in the treatment of depression , so as to tap the clinical efficacy advantages of JTP and provide data support for its clinical application. Methods: A randomized, multicenter clinical trial with parallel groups was designed in this study. A total of 40 patients with depression were included and randomly divided to either the treatment or the control group with a ratio of 1:1. The patients received JTP plus fluoxetine or fluoxetine alone once per day for 8 weeks. The primary outcome included the Hamilton Depression Rating Scale score for patients and brain structure and function by functional magnetic resonance imaging . The secondary outcomes included Traditional Chinese medicine syndrome integral scale scores, Wisconsin Card Sorting Test, blood metabonomics, urine metabonomics. Conclusion: The results of this trial will find changes in brain structure, brain function, and metabolism in patients with depression , and provide critical evidence for JTP in the treatment of depression .
机译:背景:抑郁症是一种常见的情感障碍,其特征在于标记和持久的忧郁,具有相应的思想和行为变化。由于生命的加速和增加工作压力,抑郁症的发生率急剧上升,对家庭和社会生活产生了巨大危害。焦田丸(JTP)是一种中国草药配方,通常为临床治疗中的抑郁和失眠,并表现出抗抑郁作用,如动物实验研究所示。然而,没有标准的临床试验,以确认其治疗抑郁症的功效。目的:本研究旨在评估JTP治疗抑郁症的疗效和安全性,从而挖掘JTP的临床疗效优势,并为其临床应用提供数据支持。方法:在本研究中设计了随机的,具有平行组的随机的多中心临床试验。共用40例抑郁患者并随机分为治疗或对照组,其比例为1:1。患者每天每天服用JTP加氟西汀或氟西汀8周。主要结果包括汉密尔顿抑郁率评级评级分数为患者和脑结构的尺度分数,并通过功能磁共振成像功能。二次结果包括中药综合征的积分规模分数,威斯康星州卡片分拣试验,血液代谢型,尿代谢族。结论:该试验的结果将发现抑郁症患者脑结构,脑功能和新陈代谢的变化,并为抑郁症的治疗提供了JTP的关键证据。

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