KCT0001521已完成未知
A clinical study on validity of the Qi blood Yin Yang deficiency Questionnaire for chronic fatigue
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 311
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 20(Year) 至 69(Year)（—）
- 性别
- All
入选标准
- •(1) Males and females aged 20 to 69
- •(2) The presence of unexplained chronic fatigue that is continuous for more than 6 months
- •(3) Not chronic fatigue syndrome and idiopathic chronic fatigue
- •(4) Subjects with agreements in the Korean medical doctors’ diagnoses
- •(5) Those who consent to participate in this trial and sign an informed consent statement after listening to a clear explanation of the purpose and characteristics of this clinical trial
排除标准
- •(1) Over 14 score of Perceived Stress Scale-10item (PSS-10item)
- •(2) Subjects with disagreements in the Korean medical doctors’ diagnoses
- •(3) The presence of the following conditions in the subject’s past history that might trigger chronic fatigue:
- •(a) organic causes, such as acute or chronic liver disease (for example, hepatitis, liver cirrhosis), anemia, tuberculosis, chronic lung disease, cardiovascular disease (for example, heart failure, hypertension), endocrine/metabolic disease (for example, diabetes, thyroid gland disease, severe obesity), autoimmune disease (for example, rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis), malignant tumors, or infectious disease
- •(b) psycho-social causes, such as depression, anxiety neurosis, recent severe stress, schizophrenia, alcoholism, or an eating disorder (anorexia nervosa, bulimia nervosa)
- •(4) Subjects who have taken the following drugs within the past 2 weeks: antihypertensive drugs, antidepressants, anti-anxiety agents, hypnotics, or antihistamines
- •(5) Pregnant or breast-feeding women
- •(6) Subjects who are participating in other clinical trials
- •(7) Subjects who are overworked
- •(8) Subjects who have experienced a hypersensitive reaction after clinical laboratory test
- •(9) Subjects who do not provide informed consent
- •(10) others whose clinical trial conductors are considered inappropriate for participating in this trial
研究者
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