EUCTR2008-004122-17-NL进行中（未招募）1 期
International Study to Predict Optimised Treatment - in DepressioniSPOT-D - iSPOT-D
BRC operations Pty. Ltd.0 个研究点目标入组 2,163 人开始时间: 2008年8月20日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 2,163
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- Meet DSM-IV criteria for primary diagnosis of MDD
- •- HAM-D21 score of >16.
- •Patients and controls
- •-18-65 years age-range (inclusive)
- •- Subjects with Dutch fluency.
- •- Written, informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-Presence of suicidal ideations and/or tendencies, bipolar disorder, psychosis or primary eating disorders.
- •- Pregnancy and women of child bearing potential who are not taking a medically
- •accepted form of contraception
- •- Breastfeeding.
- •-Known contra-indication to the use of Escitalopram, Sertraline or Venlafaxine XR as
- •defined in the product package insert for each drug
- •-Use of any antidepressant or CNS drug which can not be washed out prior to
- •participation.
- •-Use of any medication which is known to be contraindicated
- •- Evidence of either hyper or hypo-thyroidism within previous 3 months.
研究者
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