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临床试验/CTRI/2024/04/066519
CTRI/2024/04/066519尚未招募4 期

A Comparative Study of Efficacy and Safety of Vortioxetine with Escitalopram in Patients of Major Depressive Disorder at Tertiary Care Hospital - NI

nil0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

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

入选标准

  • 1)Adult Patients (18-65 years old) diagnosed with MDD based on DSM-5 criteria.
  • 2) Patients Presenting to the tertiary Care Hospital outpatient Department with moderate to severe symptoms.
  • 3) Willingness to Provide informed consent for participation in the study.

排除标准

  • Patients with a history of bipolar disorder, psychotic disorder, or substance abuse within the past six months.
  • Concurrent use of other antidepressants or psychotropic medications.
  • Patients with previous depression resistant to antidepressants and those who had taken treatment with ECT in previous 3 months or formal psychotherapy within 1 month.
  • Pregnancy or lactation.
  • Patients with drug intake for psychosis or anxiety.
  • Any history of allergy to the drugs.

研究者

发起方
nil

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