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临床试验/EUCTR2006-005082-19-GB
EUCTR2006-005082-19-GB进行中(未招募)1 期

Effect of an angiotensin receptor antagonist on cerebral blood flow, cerebral perfusion pressure, and systemic and peripheral haemodynamics in patients with recent stroke. - Telmisartan in Acute Stroke

Research Innovation Services, University of Nottingham0 个研究点目标入组 34 人开始时间: 2006年10月31日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
34

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • Patients must be 18 years of age or over
  • Onset date of stroke is less than 5 days.
  • Systolic BP >140mmHg.
  • Anterior circulation stroke
  • Persisting stroke symptoms at time of enrolment or visible corresponding stroke lesion on CT
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Less than 18 years of age
  • Normotension or hypotension (systolic less than 140mmHg)
  • Onset date more than 5 days
  • Coma (Scandinavian Stroke Scale (SSS) <4)
  • Patients who are of childbearing potential, pregnant or breastfeeding
  • Known bilateral renal artery stenosis (or unilateral in a single kidney)
  • TIA (defined by symptoms resolved in 24 hours with a normal CT scan)
  • Posterior circulation stroke
  • Dysphagia with no enteral access
  • Chest infection requiring continuous oxygen therapy
  • COPD requiring regular inhalers/nebulisers (mild COPD requiring PRN bronchodilators permitted)
  • Known hypersensitivity to telmisartan or angiotensin receptor blockers

研究者

发起方
Research Innovation Services, University of Nottingham

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