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

Phase 4
Recruiting
Conditions
Anxiety and depression
Registration Number
ITMCTR2100004368
Lead Sponsor
Dongfang Hospital Beijing University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(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).

Exclusion Criteria

(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.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hospital Anxiety and Depression Scale;
Secondary Outcome Measures
NameTimeMethod
Pittsburgh sleep quality index;Self-rating Depression Scale;Self-rating Anxiety Scale;TCM Syndrome Scale;TCM Constitution identification scale;FIRST-C;
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