EUCTR2006-000754-40-DE进行中（未招募）不适用
Interaktion von Statinen mit Clopidogrel als Sekundärprophylaxe bei der akuten zerebralen Ischämie - CLOPISTAT - CLOPISTAT
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 15
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
- •- Age 40 – 80 years
- •- TIA or first ischemic stroke
- •- NIHSS < 5
- •- Serumcholesterol > 5 mmol/l, Serum-LDL-C > 3 mmol/l
- •- Written informed consent
- •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
- •- Pre- treatment with ASS or other anticoagulant medication within the last 6 weeks
- •- Pre-treatment with lipid-lowering agents within the last 6 weeks
- •- Thrombolysis in acute stroke
- •- Previous stroke
- •- Malignant systemic disease
- •- Dementia
- •- Bathel-Index > 1
- •- Known liver damage or persistent ellevation of liver enzymes
- •- Known or current abuse of drugs, medications or alcohol
- •- Subjects unlikely to comply with the requirements of the protocol
- •- Pregnancy or lactation
- •- Women with child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they meet the following definition of post-menopausal: 12 month of natural (spontaneous) amenorrhea or 6 weeks post surgical bilateral oophorectomy with or without hysterectomy or are using a highly effective method of birth control (defined as those which result in a low failure rate, i.e. less than 1% per year) when used consistently and correctly such as implants, injectables, combined oral contraceptives, some IUDs, sexual abstinence or vasectomized partner
- •- Participation in another clinical trial within the last 4 weeks
研究者
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