EUCTR2008-000433-21-IT进行中（未招募）1 期
High dose atorvastatin in acute ischemic stroke ? Monocenter pilot study - ADIS 1.0
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点目标入组 150 人开始时间: 2008年3月17日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 150
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
- 性别
- All
入选标准
- •1)Clinical-radiological diagnosis of acute ischemic stroke
- •2)Onset of symptoms within 12 hours before enrolment
- •3)NIHSS >= 4
- •4)Age >= 18 years
- •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
- •1)Inability or refusal of the patient or relative to provide the informed consent
- •2)Dysphagia associated with impossibility to insert a naso-gastric tube
- •3)Thrombolytic treatment of stroke
- •4)Patient already under statin treatment
- •5)Known statin intolerance
- •6)Modified Rankin Scale > 3 before the acute stroke
- •7)Pregnancy
- •8)Malignancy
- •9)Liver cirrhosis
- •10)Chronic hepatitis
- •11)Jaundice
- •12)Alcoholism
- •13)Acute hepatic failure
- •14)Concurrent treatment with cyclosporin, erythromycin, clarithromycin, itraconazole, ketoconazole, nefazodone, niacin, gemfibrozil, other derivatives of fibric acid or inhibitors of HIV proteases.
- •15)Baseline AST or ALT or CPK > 3 fold the maximum normal limit
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