ISRCTN76657275已完成未知
Acute Candesartan Cilexetil Outcomes Stroke Trial
City Hospitals Sunderland NHS Foundation Trust (UK)0 个研究点目标入组 50 人开始时间: 2005年9月14日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Clinical diagnosis of acute ischaemic stroke within 72 hours of symptom onset (proven on CT imaging).
- •2. Medically stable with no evidence of acute infection and not receiving antibiotic therapy.
- •3. Neurologically stable with no progression on NIHSS.
- •4. Able to swallow safely and able to tolerate unthickened oral fluids without risk of aspiration.
- •5. Mean blood pressure in the unaffected arm >120/70 from three readings taken within one hour at twenty minute intervals using a calibrated Omron M5-1 BP monitor.
排除标准
- •1. Previous severe disability (Modified Rankin Score greater to or equal to 3).
- •2. Nursing home resident.
- •3. Previous history of congestive cardiad failure requiring treatment with an ACE inhibitor or Angiotensin Receptor Blocker (ARB).
- •4. Renal impairment (defined serum creatinine >200 umol/l).
- •5. Women of child bearing potential.
- •6. Minors aged less than 18.
- •7. History of evidence of dementia without capacity for consent.
研究者
相似试验
Unknown
4 期
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Scandinavian Candesartan Acute Stroke Trial - SCASTAcute stroke (ischemic or haemoragic)EUCTR2004-002187-22-SEllevål University Hospital2,500
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Scandinavian Candesartan Acute Stroke Trial - SCASTAcute stroke (ischemic or haemoragic)EUCTR2004-002187-22-DEllevål University Hospital2,600
