CTRI/2019/01/017302招募中4 期
A comparative study of efficacy, safety and onset of action of vilazodone with escitalopram in patients of major depressive disorder at tertiary care hospital.
Dr Ankushe rohini0 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
- 招募中
- 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)Patients of either sex with age between 18 to
- •2)Newly diagnosed MDD patients meeting DSM- 5
- •criteria for depression.
- •3)Patient who give written informed consent.
排除标准
- •1)Pregnant or nursing women.
- •2)Patients with high risk of suicidal tendency
- •or previous suicide attempt within 6 months.
- •3)Patients with bipolar disorder, drug abuse or
- •dependency, post traumatic stress disorder,
- •obsessive â?? compulsive disorder.
- •4)Patients with previous depression resistant to
- •antidepressants and those who had taken treatment
- •with electroconvulsive therapy in previous 3
- •months or formal psychotherapy within 1 month.
- •5)Patients on other antidepressants.
- •6)Patients with neurological disorders (dementia,
- •seizures, stroke), obesity with functional
- •impairment, serious or unstable organic disorder
- •(neoplasia, cardiovascular, pulmonary,uncontrolled
- •type 1 or 2 diabetes).
- •7)Any other medical disorder which is confounding
- •our inclusion diagnosis.
- •8)Patients with drug intake for psychosis or anxiety.
- •9)Any history of allergy to the drugs.
研究者
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