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临床试验/NCT01258231
NCT01258231招募中不适用

Identification of Genomic Predictors of Adverse Events After Cardiac Surgery

Brigham and Women's Hospital3 个研究点 分布在 1 个国家目标入组 4,000 人开始时间: 2000年8月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
4,000
试验地点
3
主要终点
Mortality (i.e. number of participants who are deceased during postoperative day 0 up to year 5)

研究概览

简要总结

This study aims to identify genetic causes of adverse events after cardiac surgery, such as atrial fibrillation, myocardial infarction, renal dysfunction and heart failure.

Patients undergoing heart surgery at Brigham and Women's Hospital and Texas Heart Institute are eligible to participate.

详细描述

This study aims to identify genetic causes of adverse events after cardiac surgery, such as atrial fibrillation, myocardial infarction, renal dysfunction and heart failure. In addition, we also examine blood and urine biomarkers (proteins).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
20 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Undergoing heart surgery
  • Willing to provide consent

排除标准

  • Enrolled in a concurrent drug or device trial that precludes concurrent enrollment

结局指标

主要结局

Mortality (i.e. number of participants who are deceased during postoperative day 0 up to year 5)

时间窗: Day of procedure to year 5

Data will be collected from electronic medical records; data points to be collected for this measurement include serum creatinine.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jochen Daniel Muehlschlegel, MD

Professor

Johns Hopkins University

研究点 (3)

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