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临床试验/KCT0007272
KCT0007272尚未招募未知

Randomized Controlled Study to Evaluate Safety and Efficacy of Banhahubaktang in Patients with Depression

Kyung Hee University Oriental Medical Center0 个研究点目标入组 84 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
84

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
19(Year) 至 65(Year)(—)
性别
All

入选标准

  • 1. K-HDRS score of 18 or higher
  • 2. Men and women between the ages of 19 and 65
  • 3. Volunteered to participate and signed the consent form
  • 4. Diagnosed with major depressive disorder of DSM-V

排除标准

  • 1. At risk of suicide
  • 2. K-HDRS score of 27 or higher
  • 3. Diagnosed with major depressive disorder who require hospitalization
  • 4. Patients who have received electrotherapy, vagus nerve stimulation, deep brain stimulation, phototherapy, transcranial magnetic stimulation, or psychotherapy within the past 3 months
  • 5. Panic disorder, obsessive compulsive disorder, post-traumatic stress disorder, antisocial personality disorder, borderline personality disorder, theatrical personality disorder, or other severe personality disorder (paranoid, schizoid, narcissistic, avoidant, dependent personality disorder, etc.)
  • 6. Manic episodes, hypomanic episodes, or mixed episodes
  • 7. Abuse/dependence on alcohol or other substances
  • 8. Use of substances or drugs that can affect the severity of depression (eg, anti-anxiety drugs, antidepressants, antipsychotics, corticosteroids, female hormones, L-dopa, Digitalis, bromide, cyclosporin, disulfiram, isoniazid, yohimbine, etc. that are being administered alone or as multiple (combination therapy) (except when 4 weeks have elapsed since the last dose of the drug at the time of screening)
  • 9. Use of a thrombolytic or anticoagulant
  • 10. Medical conditions that may affect the severity of depressive symptoms (e.g., myocardial infarction, arrhythmia, brain tumor, multiple sclerosis, pancreatic disease, hypothyroidism/hyperthyroidism, hyperparathyroidism, Addison's disease, Cushing's disease, rheumatism) Arthritis, cancer, cerebrovascular disease, dementia, epilepsy, etc.)
  • 11. Chronic diseases that are not well controlled despite appropriate treatment (chronic active hepatitis, high blood pressure, diabetes, etc.), Poorly controlled hypertension refers to a condition in which blood pressure is not controlled below 140/90 mmHg even after three or more antihypertensive drugs have been administered in sufficient dose and combination of appropriate drugs including diuretics. It refers to a state in which HbA1c = 9.0% is maintained despite the combination of and administration at a sufficient dose.
  • 12. Being treated for liver cancer, cirrhosis, chronic renal failure, etc. or are being treated for congestive heart failure classified as NYHA Class III-IV
  • 13. Hepatic and renal dysfunction (at screening, ALT, AST, ALP = 2 times the upper limit of normal or creatinine > 2.0 mg/dL)
  • 14. Genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
  • 15. A disease that may affect drug absorption or have digestive problems after related surgery
  • 16. Enrollment in another clinical trial within 1 month before the start of the study
  • 17. Hypersensitivity or allergy to research-related drugs
  • 18. Use of herbal medicines or herbal preparations other than this investigational drug
  • 19. Those who do not understand the consent form or have difficulty in continuing research due to mental retardation or intellectual problems
  • 20. Pregnant or lactating women
  • 21. Those who are pregnant and do not agree to the accepted contraceptive methods (dual contraception*, intrauterine contraceptive device and spermicide) during the clinical trial period
  • *Double contraception refers to the case of using hepatic contraception (condoms, diaphragm, etc.) together with other contraceptive methods (sterilization, intrauterine contraceptive device, contraceptive cream, jelly or foam, etc.).
  • 22. In case the investigator is determine inappropriate to participate in the clinical trial due to other reasons

研究者

发起方
Kyung Hee University Oriental Medical Center

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