CTRI/2014/03/004453招募中4 期
A randomized study of the cost effectiveness and tolerability of escitalopram and desvenlafaxine in treatment of moderate to severe depression
Moulya Nagraj0 个研究点目标入组 60 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
- 入组人数
- 60
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
- •Subjects of either gender aged between 18-65 years.
- •Subjects with first episode or recurrent episode of depression according to (ICD-10) with baseline score >18 and < 40 according to MADRS.
- •Willingness to give written informed consent and available for follow up.
排除标准
- •Atypical depression
- •Postpartum depression
- •Pregnant women, breast feeding and women planning to conceive.
- •Subjects with severe depression requiring ECT and with high risk of suicidal tendency.
- •Co-morbid psychiatric illnesses
- •Previous history of epilepsy and sexual dysfunction
- •Serious or uncontrolled medical illness like glaucoma, hypertension, diabetes mellitus, hyperlipidemia, myocardial infarction, hepatic and renal impairment.
- •Depression secondary to medical illnesses, post traumatic depression.
- •Known history of allergy to both the study medications.
- •Participation in any other research study in recent past
研究者
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