NL-OMON54160已完成不适用
CONTINUOUS POSTOPERATIVE PERICARDIAL FLUSHING AFTER GENERAL CARDIAC SURGERY PROCEDURES WITH THE HAERMONICS INVESTIGATIONAL DEVICE : STUDY PROTOCOL OF THE FLUID (FLUsh with Investigational Device) TRIAL - The FLUID trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 992
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Adults undergoing a general cardiothoracic surgery procedure with the use of
- •cardiopulmonary bypass are eligible for participation
排除标准
- •Euroscore II > 20% , Intraoperatively diaphragm injury leading to an open
- •connection between the thoracic and abdominal cavity, Age < 18, Inability to
- •understand study information, Participation in any study involving an
- •investigational drug or device, Emergent procedures, Procedures performed off
- •pump, without the use of cardiopulmonary bypass, Minimal invasive cardiac
- •surgery procedures (e.g. minithoracotomy and hemisternotomy)
研究者
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