Simvastatin in Aneurysmal Subarachnoid Haemorrhage (STASH) a Multicentre Randomised Controlled Clinical Trial
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
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
1
placebo
干预措施: placebo (Drug)
11
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
Mr PJ Kirkpatrick
Consultant Neurosurgeon
Cambridge University Hospitals NHS Foundation Trust
