EUCTR2006-000369-12-DE进行中（未招募）不适用
An open, randomized, single-center study assessing the serum time-concentration curves and the effect of prophylactic moxifloxacin (in comparison with cefuroxime) on the early inflammatory response to cardiopulmonary bypass in patients undergoing coronary artery bypass grafting - Moxi and CPB
Institute of Anaesthesiology, German Heart Centre0 个研究点目标入组 30 人开始时间: 2006年3月6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
- 30
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
- •coronary artery disease scheduled for coronary artery bypass grafting with cardiopulmonary bypass
- •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
- •- Body mass index > 30
- •- Ejection fraction < 50 %
- •- Severe cardiac arrhythmias (long QT syndrome) or intake of drugs which prolong the QT interval (available from: http://www.torsades.org)
- •- Renal and hepatic dysfunction, evaluated by serum creatinine and SGOT/SGPT values above the normal range
- •- Intake of corticosteroids
- •- Allergies to quinolones, cephalosporins, aprotinin, or other drugs leading to the decision to omit these drugs or to give prophylactic antihistamines and corticosteroids
- •- Antibiotic therapy or infectious disease until 2 weeks before start of the trial
- •- Women who are pregnant (women with childbearing potential must have a negative pregnancy test) and nursing mothers
- •- Tendinopathies caused by quinolones
- •- Seizures
研究者
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