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临床试验/ACTRN12613000112763
ACTRN12613000112763已完成3 期

Youth Depression Alleviation: Augmentation with Anti-inflammatory Agent (YoDA-A)Proof of principle of the inflammatory and oxidative theory of depression: A treatment study of rosuvastatin and aspirin

Orygen, the National Centre of Excellence in Youth Mental Health, The University of Melbourne0 个研究点目标入组 130 人开始时间: 2013年1月30日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
130

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
15 Years 至 25 Years(—)
性别
All

入选标准

  • aged of 15 to 25 years inclusive
  • - have a diagnosis of current Major Depressive Disorder (MDD) using Structured Clinical Interview for DSM-IV Axis I Disorders (SCID)
  • - a score on the Montgomery-Asberg Depression Rating Scale of >/=20
  • - ability to give informed consent and comply with study procedures
  • - female participants are required to use effective contraception if sexually active
  • - established fluency in English
  • - if currently on treatment, that treatment (either pharmacological or psychosocial) needs to be stable treatment for at least two weeks prior to enrolment

排除标准

  • - First episode psychosis (at least one positive symptom occurring daily for at least one week, or at least three times per week if the symptom lasts for longer than one hour on each occasion)
  • - SCID-I/P diagnosis of diagnosis of bipolar I or II disorder or alcohol dependence
  • - acute or unstable systemic medical disorder (determined by the treating physician including the review of the routine bloods assessment), including abnormal liver function, thyroid function or haematological findings; or acute or unstable systemic medical disorder, including immune disorders, bleeding disorders (such as haemophillia), significant gastric pathology (e.g. gastric haemorrhage, erosive gastritis or active peptic ulcer disease) and pre-existing cardiac disease
  • - inability to comply with the requirements of informed consent or the study protocol (such as incapacity to consent, determined by the treating physician and research team)
  • - current regular (>weekly) use of statins, aspirin, NSAID’s paracetamol, corticosteroids or any other immunomodulatory agents
  • - Currently taking hypolipidaemics (e.g. gemfibrozil, nicotinic acid; cyclosporine), vitamin K antagonists and other anticoagulants (e.g. warfarin), protease inhibitors (including ritonavir), antacids (within 2 hrs); ketoconazole; spirinolactone; or cimetidine
  • - participants with a history of intolerance or allergy to study medications and those who are currently pregnant or breast feeding will also be excluded

研究者

发起方
Orygen, the National Centre of Excellence in Youth Mental Health, The University of Melbourne

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