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临床试验/IRCT2016102430459N1
IRCT2016102430459N1已完成未知

Efficacy of a herbal syrup containing Lavandula angustifolia and Cuscuta chinensis versus citalopram in MDD with anxious distress, a double blind randomized clinical trial

Vice Chancellor for research, School of Traditional Medicine, Tehran University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 60 years(—)
性别
All

入选标准

  • 1. Age between 18 to 60 years old
  • 2. Presence of Major Depressive Disorder, with anxious distress based on DSM-5 criteria
  • 3. Scores lower than 18 in the Hamilton Rating Scale for Depression.
  • 4. Scores lower than 24 in the Hamilton Rating Scale for Anxiety
  • Exclusion criteria:
  • 1. The presence of psychotic symptoms, current or past history of Bipolar disorder, Schizophrenia and Schizotypal personality disorder
  • 2. Receiving psychotropic medications or any antidepressants during the past 14 days
  • 3. The presence of an unstable disorder, Kidney or Liver failure, malignancy, Thyroid problems, Diabetes, past history of Epilepsy, bleeding disorders
  • 4. Nursing and pregnant women, reproductive age without a contraception method
  • 5. Substance abuse or addiction in the past 3 months
  • 6. Suicidal tendency in the past year, scores greater than 2 on the Suicide item of the Hamilton Rating Scale for Depression
  • 7. Women who are receiving OCP
  • 8. Any clinically significant deterioration in the condition of the subject from baseline detected by the attending physician
  • 9. Current or past history of Cognitive disorder in the past year
  • 10. ECT during the past 3 months
  • 11. Psychotherapy in the past month
  • 12. A past history of allergy towards Lavender, Chinese dodder and Citalopram

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research, School of Traditional Medicine, Tehran University of Medical Sciences

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