研究疾病:
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焦虑抑郁状态
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研究疾病代码:
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Target disease:
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Anxiety and depression
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Target disease code:
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研究类型:
Study type:
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干预性研究
Interventional study
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研究设计:
Study design:
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随机平行对照
randomized controlled trial(parallel group design)
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研究所处阶段:
Study phase:
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上市后药物
Post-marketing clinical trial
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研究目的:
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探究解郁丸的有效性及安全性,为其提供循证依据,以期为疫情期间焦虑抑郁状态的应对提供有效参考,从而改善疫情应激状态下群众的精神心理健康状况。
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Objectives of Study:
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Objective to explore the effectiveness and safety of Jieyu pill, and provide evidence-based basis for it, so as to provide effective reference for coping with anxiety and depression during the epidemic period, so as to improve the mental and psychological health of the masses under the epidemic stress state.
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药物成份或治疗方案详述:
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药物成分:白芍、柴胡、当归、郁金、茯苓、百合、合欢皮、甘草、小麦、大枣。
对照组给予心理支持治疗和相关咨询、辅导及相关知识宣教。
观察组在对照组心理支持治疗的基础上给予解郁丸,郑州豫密药业股份有限公司生产,制剂为水丸,每次4g,每日3次,温水送服。
疗程6周。
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Description for medicine or protocol of treatment in detail:
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Ingredients: Radix Paeoniae Alba, Radix Bupleuri, angelica, Curcuma, Poria cocos, lily, Albizzia julibrissin, liquorice, wheat, jujube.
The control group was given psychological support treatment and related counseling, counseling and related knowledge education.
The observation group was given Jieyu pill, produced by Zhengzhou Yumi Pharmaceutical Co., Ltd., on the basis of psychological support treatment in the control group. The preparation was water pill, 4G each time, three times a day, and delivered with warm water.
The course of treatment was 6 weeks.
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纳入标准:
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(1) 自愿签署知情同意书,并愿意配合参与研究;
(2) 焦虑抑郁状态受新冠肺炎疫情影响;
(3) 医院焦虑抑郁量表总分≥16分,且焦虑和/或抑郁条目总分≥8分;
(4) 符合肝气郁结证证候诊断;
(5) 年龄18-65岁(包含18岁和65岁)。
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Inclusion criteria
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(1) They voluntarily signed informed consent and were willing to participate in the research;
(2) novel coronavirus pneumonia affects the state of anxiety and depression;
(3) The total score of hospital anxiety and depression scale was more than 16, and the total score of anxiety and / or depression items was more than 8;
(4) According to the diagnosis of liver qi stagnation syndrome;
(5) Age: 18-65 years old (including 18 years old and 65 years old).
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排除标准:
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(1) 兴奋药物过量、催眠镇静药物或抗焦虑药的戒断反应,急性惊恐障碍、强迫症、躁狂症或精神分裂症等伴发的患者;
(2) 符合焦虑症或抑郁症诊断的患者;
(3) 既往有自杀史或有自杀倾向的患者;
(4) 器质性精神障碍、精神活性物质、非成瘾物质及产后所致的抑郁患者;
(5) 合并心、脑、肝、肾、造血、泌尿生殖等系统严重原发性疾病患者;
(6) 入组前4周内曾使用过抗抑郁、抗焦虑、抗精神病西药以及同类中药治疗的患者;
(7) 对试验用药物任何成分过敏或过敏体质者(对两种以上食物或药物过敏者);
(8) 妊娠或准备妊娠及哺乳期妇女;
(9) 入组前1个月内参加或正在参加其他临床试验的患者。
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Exclusion criteria:
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(1) Patients with overdose of excitatory drugs, withdrawal reaction of hypnotic sedative drugs or anti anxiety drugs, and patients with acute panic disorder, obsessive-compulsive disorder, mania or schizophrenia;
(2) Patients with anxiety disorder or depression diagnosis;
(3) Patients who have suicide history or suicide tendency in the past;
(4) Patients with organic mental disorders, psychoactive substances, non addictive substances and postpartum depression;
(5) Patients with severe primary diseases of heart, brain, liver, kidney, hematopoiesis and urogenital system;
(6) The patients who had used antidepressant, anti anxiety, antipsychotic western medicine and the same kind of traditional Chinese medicine treatment within 4 weeks before enrollment;
(7) Those who are allergic to any component of the test drug or allergic constitution (allergic to more than two kinds of food or drugs);
(8) Pregnant or preparing for pregnancy and lactation;
(9) Patients who participated in or were participating in other clinical trials within one month before enrollment.
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研究实施时间:
Study execute time:
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从From
2020-11-15
至To
2021-10-15
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征募观察对象时间:
Recruiting time:
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从From
2020-11-15
至To
2021-07-15
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