EUCTR2007-003218-33-DK进行中(未招募)不适用
Antitrombotisk effekt af ADP receptor inhibitor i tillæg til Aspirin til hyperkoagulable patienter der gennemgår CABG kirurgi.
Blood bank, Rigshospitalet, University Hospital of Copenhagen0 个研究点目标入组 130 人开始时间: 2007年7月24日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 130
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
- •·Patients undergoing elective CABG surgery in cardiopulmonary bypass
- •·Age > 18 years and able to give informed consent
- •·Stable vital signs within normal reference range (pulse within 20% of preoperatively, blood pressure within 10% of preoperatively, respiration frequency <18 breaths/min, normal consciousness) on the 1st postoperative day at time of inclusion
- •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.Age < 18 years
- •2.Cardiovascular
- •·ST-segment elevation myocardial infarction within 48 hours prior to randomization.
- •·Prior CABG within previous 4 weeks of randomization.
- •·Cardiogenic shock.
- •·Postoperative need for vasopressor and/or inotropic support postoperatively
- •3.Prior or concomitant therapy.
- •·Concurrent treatment with warfarin.
- •4.Hemorrhage risk
- •·History of bleeding diathesis or evidence of active abnormal bleeding within 30 days of randomization.
- •·Known haemophilia or thrombocytopathy (Glanzman´s thrombastenia, Bernard-Souliers sdm)
- •·History of hemorrhagic stroke at any time or stroke or TIA of any etiology within 30 days of randomization.
- •·Major surgery within 6 weeks prior to randomization.
- •·Known platelet count of <150,000/mm3.
- •·PT > 1.5 x control
- •·HCT < 25%
- •·Clinical signs of ongoing bleeding at time of inclusion (occult or overt)
- •·Known allergy or contraindication to aspirin or clopidogrel.
- •·Participation in a study of experimental therapy or device within prior 30 days.
- •·Creatinine level of greater than 4.0 mg/dl.
- •·Liver disease evidenced by ASAT/ALAT > 1.5 times normal
- •·Known history of alcohol or drug abuse.
- •·Pregnant women or women of child-bearing potential.
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