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临床试验/ITMCTR2100004368
ITMCTR2100004368招募中4 期

Clinical study on the efficacy and safety of Jieyuwan in the treatment of epidemic stress, anxiety and depression (stagnation of liver Qi syndrome)

Dongfang Hospital Beijing University of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 65(—)
性别
All

入选标准

  • (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).

排除标准

  • (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.

研究者

发起方
Dongfang Hospital Beijing University of Chinese Medicine

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