EUCTR2014-000952-26-GB进行中(未招募)1 期
Dual Antiplatelet Therapy to Inhibit Coronary Atherosclerosis and Myocardial Injury in Patients with Necrotic High-risk Coronary Plaque Disease - DIAMOND - Dual Antiplatelet Therapy to Reduce Myocardial Injury
niversity of Edinburgh0 个研究点目标入组 202 人开始时间: 2014年7月4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
- 202
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
入选标准
- •1) Patients aged =40 years with angiographically proven multivessel coronary artery disease defined as at least two major epicardial vessels with any combination of either (a) >50% luminal stenosis, or (b) previous revascularization (percutaneous coronary intervention or coronary artery bypass graft surgery).
- •2) Provision of informed consent prior to any study specific procedures
- •3) Receiving aspirin
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 100
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 150
排除标准
- •1.An acute coronary syndrome within the last 12 months
- •2.An indication for dual anti-platelet therapy, such as drug eluting stent
- •3.Receiving thienopyridine therapy such as clopidogrel or prasugrel
- •4.Percutaneous coronary intervention or coronary artery bypass graft surgery within the last 3 months
- •5.Inability or unwilling to give informed consent
- •6.Women who are pregnant, breastfeeding or of child-bearing potential (women who have experienced menarche, are pre-menopausal and have not been sterilised) will not be enrolled into the trial
- •7.Known hypersensitivity to ticagrelor or one of its excipients
- •8.Active pathological bleeding or bleeding diathesis
- •9.Significant thrombocytopenia: platelets <100 x 109 /L
- •10. History of intracranial haemorrhage
- •11.Moderate to severe liver impairment (Child’s Grade B or C)
- •12.Maintenance therapy with strong CYP3A4 inhibitors, such as ketoconazole, nefazodone, ritonavir, indinavir, atazanavir, or clarithromycin
- •13.Major intercurrent illness or life expectancy <1 year
- •14.Renal dysfunction (eGFR =30 mL/min/1.73 m2)
- •15.Contraindication to iodinated contrast agents
- •16.Planned coronary revascularization or major non-cardiac surgery in the next 12 months
- •17. Maintenance therapy with simvastatin or lovastatin at doses greater than 40mg daily
- •18.Receiving oral anticoagulants including warfarin, rivaroxaban, dabigatran or apixaban.
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