跳至主要内容
临床试验/NCT00848770
NCT00848770Unknown不适用

Manipulation of Arterial Pressure Early in Non Thrombolysed Acute Ischemic Stroke: Effects on Death and Neurological Disability

Hospital de Clinicas de Porto Alegre1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
240
试验地点
1
主要终点
Ranking score and mortality

研究概览

简要总结

This is a controlled clinical trial among non thrombolysed acute ischemic stroke patients to determine the effects of three levels of arterial pressure on death and neurological disability. After the admission in the vascular unit of the Emergency Department the patients are randomized to maintain during the first 24h the Systolic Arterial Pressure in tree levels of pressure: 140 to 160 mmHg; 161 to 180 mmHg and 181 to 200 mmHg. The end point of the study is the Modified Rankin score and mortality in three month after the discharge.

详细描述

To maintain the tree levels of systolic arterial pressure during de first 24h we will use one of the two strategies:1) infusion of 500 to 1000ml of saline solution and/or norepinephrine solution to increase de systolic pressure or 2) infusion of esmolol or nitroprussiate solution to decrease de pressure. Every patient will have a transcranial doppler study in the first 24h to measure the mean velocity of cerebral arteries.

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
None

入排标准

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

入选标准

  • Patients 18 years or older, with the first Acute Ischemic Stroke within the first 6 hours of the symptoms and not candidate to thrombolysis
  • We will also include patients with previous Ischemic Stroke with Ranking score 0 or 1

排除标准

  • Improuvment of the symptoms rapidly (in the first 15 min after admission)
  • Seizures not related do the acute ischemic stroke
  • Previous ischemic stroke in the last 6 weeks and with Ranking score > 1
  • Haemorrhagic stroke
  • Anticoagulation
  • Hypoglycemia
  • Acute heart failure

研究组 & 干预措施

1, 140 to 160 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: Esmolol, Sodium Nitroprussiate (NPS) or Norepinephrine (NOR) (Drug)

1, 140 to 160 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: Esmolol, NPS or NOR (Drug)

1, 140 to 160 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: manipulation of SAP (Drug)

2, 161 to 180 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: Esmolol, Sodium Nitroprussiate (NPS) or Norepinephrine (NOR) (Drug)

2, 161 to 180 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: Esmolol, NPS or NOR (Drug)

2, 161 to 180 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: manipulation of SAP (Drug)

3, 181 to 200 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: Esmolol, Sodium Nitroprussiate (NPS) or Norepinephrine (NOR) (Drug)

3, 181 to 200 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: Esmolol, NPS or NOR (Drug)

3, 181 to 200 mmHg

Active Comparator

Esmolol, NPS or NOR

干预措施: manipulation of SAP (Drug)

结局指标

主要结局

Ranking score and mortality

时间窗: Three month

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

Loading locations...

相似试验