EUCTR2012-005803-42-SE进行中（未招募）不适用
Evaluation of platelet function following cessation of ticagrelor - a study in patients with acute coronary syndrome and PCI with coronary stent
niversitetssjukhuset Örebro0 个研究点开始时间: 2013年1月31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
- •1. 12 months (+/- one week) treatment with double platelet blockade in the form of ASA and ticagrelor following PCI
- •2. Age = 45 years
- •3. Signed and dated Informed Consent
- •4. The subject is willing and judged capable of following the protocol throughout the study
- •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 0
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •1. Resistance against ticagrelor treatment (so-called non-responders”)
- •2. Other oral anti-platelets agents other than ticagrelor 180 mg and ASA 75 mg/day
- •3. Concurrent treatment with fluvoxamine, fluoxetine, moklobemide, voriconazole, fluconazole, ticlopidine, ciprofloxacin, cimetidine, carbamazepine, oxkarbazepine or chloramphenicol.
- •4. Oversensitivity/allergy to ticagrelor
- •5. Pregnancy or breastfeeding
研究者
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