EUCTR2020-002787-32-GB进行中(未招募)1 期
Antidepressant for the prevention of DEPression following first episode Psychosis trial - ADEPP
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 508
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 first-episode psychosis (FEP).
- •Within 3 months of initial treatment for FEP (as defined by onset of care provision by an Early Intervention Team).
- •Positive and Negative Syndrome Scale (PANSS) individual positive item scores all = 4.
- •Sufficiently recovered from acute psychotic episode with capacity to consent.
- •Aged 18-35 years.
- •Currently prescribed antipsychotic medication at stable dose.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 508
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Current moderate or severe depression (as indicated by a Calgary Depression for
- •Schizophrenia Scale (CDSS) score of >7).
- •Currently prescribed antidepressant medication (or within 2 weeks of stopping if a Monoamine Oxidaise Inhibitor)
- •Previous history of mania.
- •Contraindications to selective serotonin reuptake inhibitors (SSRI) antidepressant treatment (e.g. recurrent thrombotic illness, previous adverse reaction, confirmed pregnancy, although risk in pregnancy is low, prescribed pimozide).
- •Serious medical or neurological illness (as identified by the treating consultant psychiatrist).
- •Electrocardiogram (ECG): QTc interval >450 as measured in the last 12 months.
- •Aged below 18 years
- •Aged over 35 years
研究者
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