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临床试验/ISRCTN76657275
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

发起方
City Hospitals Sunderland NHS Foundation Trust (UK)

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