EUCTR2010-020185-19-DE进行中（未招募）1 期
Optimization of Treatment and Management of Schizophrenia in Europe - the optimise trial
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 500
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
- •Diagnosis of schizophrenia, schizophreniform or schizoaffective disorder as defined by DSM-IV on the basis of the Mini International Neuropsychiatric Interview Plus (M.I.N.I. Plus; Sheehan et al. 1998).
- •Age 18-40 years
- •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 500
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •A time interval between the onset of positive symptoms (hallucinations and/or delusions) and study entry exceeding two years.
- •Prior use of antipsychotic medication longer than an episode of two weeks in the previous year and/or 6 weeks lifetime.
- •Intolerance to one of the drugs in this study.
- •Patients who are coercively treated at a psychiatric ward (based on a judicial ruling)
- •Patients who are represented by a legal ward or under legal custody
- •The presence of one or more of the contraindications against any of the study drugs as mentioned in the IB texts
- •Pregnancy or lactation
研究者
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