EUCTR2015-001092-49-SE进行中（未招募）不适用
Valproic acid regulation of plasma PAI-1
Sahlgrenska Akademien Wallenberglaboratoriet0 个研究点开始时间: 2015年3月30日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •For all subjects:
- •1.Subect has given informed consent
- •2.Men and women aged 20 -85 years
- •3.Non smoker
- •Additional for patients with coronary artery disease:
- •4.Pronounced atherosclerosis
- •5.Treatment for acute myocardial infarction for more than a year ago
- •6.Only Trombyl (no other anticoagulant therapy)
- •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 50
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •2.BMI (body mass index) >35 kg / m²
- •3.Epilepsy
- •4.Uncontrolled hypertension
- •5.Malignancy
- •6.Mental disorder
- •7.Alcoholism
- •8.All forms of chronic illness with medications that are contraindicated to combine with Ergenyl
- •9.Acute infection
- •10.Difficulties in implementing the study with regard to the inability to lie still on a gurney because of the general condition or obvious difficulty with putting vein / artery catheter
- •11.Interaction with Ergenyl
- •12.Known hypersensitivity to valproic acid or other component included
- •13.Ongoing or planned pregnancy within the next 3 months
- •14.Breastfeeding women
- •15.Suspected or actual inability to perceive the study of information and instruction
研究者
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