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临床试验/NCT00731627
NCT00731627已完成3 期

Simvastatin in Aneurysmal Subarachnoid Haemorrhage (STASH) a Multicentre Randomised Controlled Clinical Trial

Cambridge University Hospitals NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 803 人开始时间: 2007年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
803
试验地点
2
主要终点
Modified Rankin Disability Score (mRS) at 6 months

研究概览

简要总结

Intracranial bleeding from ruptured blood vessels (called a subarachnoid haemorrhage -SAH) affects 7000 patients each year in the UK and is a source of considerable death and disability, even in young adults. Recent observations indicate that these bleeds can cause reduced cerebral blood flow which leads to a bad outcome. High rates of death and disability occur, and are particularly prevalent when low cerebral blood flow results in stroke. Prevention of cerebral artery spasm and improvement in blood vessel reflexes are the target of modern therapy. Candidate drugs include statins which have an impeccable safety record and multiple potential beneficial actions (improve cerebral blood flow, reduce inflammatory processes, reduce adverse blood coagulation) following SAH.

The investigators plan to use a statin, Simvastatin (40 mg) to improve cerebral blood flow and reduce inflammation. We have already completed a phase 11 study (n=80) which demonstrated potential benefits for acute statin therapy following SAH, and the investigators now wish to conduct a multi-centre phase 111 study to explore any potential clinical benefits in a larger population (n=1600). The purpose is to see whether the positive effects of statins seen in our phase II study translate into clinical benefits - both short term (e.g. reduced need for intensive care) and long term (outcome and wellbeing at 6 months).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

1

Placebo Comparator

placebo

干预措施: placebo (Drug)

11

Active Comparator

simvastatin

干预措施: simvastatin (Drug)

结局指标

主要结局

Modified Rankin Disability Score (mRS) at 6 months

时间窗: 6-12 months

次要结局

  • Need and intensity of delayed ischaemic deficit rescue therapy(1-3 months)
  • Incidence and duration of delayed ischaemic deficits(1-3 months)
  • Incidence and severity of sepsis(1-3 months)
  • Length of intensive care and total acute hospital stay(1-3 months)
  • Discharge destination(1-3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mr PJ Kirkpatrick

Consultant Neurosurgeon

Cambridge University Hospitals NHS Foundation Trust

研究点 (2)

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