ACTRN12621000181808进行中（未招募）3 期
The PRESIDE (PhaRmacogEnomicS In Depression) Trial: a double-blind RCT ofpharmacogenomically-informed prescribing of antidepressants on depression outcomes inpatients with major depressive disorder in primary care.
适应症
试验速览
- 阶段
- 3 期
- 状态
- 进行中（未招募）
- 入组人数
- 575
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 65 Years（—）
- 性别
- All
入选标准
- •Eligible participants for the trial are aged between 18 and 65 years old
- •Participants able to read and write English and competent to give informed consent
- •Participants who are contactable over the next 6 months for the study follow-up
- •Symptoms of depression - identified in the PHQ-9 initial screening questionnaire (iPad/phone delivery).
排除标准
- •currently taking antipsychotic medication, except if taking quetiapine (Seroquel) at a dose of 100mg at most PRN for sleep, with no history of psychosis
- •significant suicidal risk
研究者
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