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临床试验/CTRI/2017/11/010443
CTRI/2017/11/010443已完成4 期

Comparative study on Efficacy and safety profile of Amitriptyline and Fluoxetine in patients with depression

svasanth0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1.19years â?? 60 years of age both sex
  • 2.newly diagnosed patients with clinical depression (moderate to severe ) according to ICD 10 criteria
  • 3. Major depressive disorder patients.

排除标准

  • 1.Less than 19 years
  • 2. more than 60 years.
  • 3.Pregnant and Lactating mothers.
  • 4.Patients with h/o Cardiac , Hepatic and renal disease ,Co morbid illness and terminal illness.
  • Known case of Pulmonary Tuberculosis, HIV/AIDS, Leprosy, Hypothyroidism.
  • Patients with history of hypersensitive reaction to Amitriptyline and Fluoxetine.
  • Patients on any other investigational drugs.
  • Depression with psychosis, bipolar depression .

研究者

发起方
svasanth

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