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临床试验/IRCT201509201556N82
IRCT201509201556N82已完成3 期

Comparison of saffron and fluoexetine in the treatment of mild to moderate post partum depression :A duble –blind clinical trial

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
3 期
状态
已完成
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 45 years(—)
性别
Female

入选标准

  • Presence of Major Depressive Disorder; with peripartum onset based on DSM-5 criteria; age between 18 to 45 years old; score lower than 18 in Hamilton Rating Scale for depression. Exclusion criteria: -Psychotic symptoms or any other major psychiatric disorder; receiving any antidepressants during past one month or ECT during past two months; Presence of hypothyroidism or hyperthyrodism; srious suicidality or infanticide ideas; substance abuse or dependence uring the last three months

排除标准

  • 未提供

研究者

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