跳至主要内容
临床试验/NCT01103908
NCT01103908终止不适用

Ultrasound Dilution Cardiac Output at the Conclusion of Cardiopulmonary Bypass in Pediatric Patients

Transonic Systems Inc.1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2010年4月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
3
试验地点
1
主要终点
Cardiac output after cardiopulmonary bypass

研究概览

简要总结

Cardiac output, the amount of blood pumped by the heart in one minute, will be measured in pediatric patients undergoing surgery involving cardiopulmonary bypass (CPB). Cardiac output will be measured after cardiopulmonary bypass using a device that employs ultrasound dilution technology. At times, cardiac output will be measured during a procedure called modified ultrafiltration (MUF). The ultrasound dilution cardiac output measurements will be validated or compared with cardiac output measurements made using other FDA approved techniques and devices.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
— 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Pediatric patients (age < 21 years)
  • Pediatric patients undergoing surgery involving cardiopulmonary bypass

排除标准

  • Patients aged > 21 years
  • Patients undergoing surgery "off pump" (not involving cardiopulmonary bypass)

结局指标

主要结局

Cardiac output after cardiopulmonary bypass

时间窗: Less than 10 minutes

Cardiac output will be measured in pediatric patients after undergoing surgery involving cardiopulmonary bypass

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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