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
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