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临床试验/NCT01610622
NCT01610622已完成不适用

Estimation of Cardiac Output in Neonatal ICU Using an Ultrasound Dilution Technique

Transonic Systems Inc.1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2012年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
7
试验地点
1

研究概览

简要总结

Presently there is no apparatus, clinically available, for routine determination of cardiac output (CO) in children. The goal of this research is to develop new technology that will help determine CO in neonates.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
— 至 1 Month(Child)
性别
All
接受健康志愿者

入选标准

  • All neonatal patients cared for in our ICU with umbilical venous and arterial catheters simultaneously in place for their care, will be eligible.

排除标准

  • Patients would be excluded if the family/guardian denied permission or if the attending physician felt the patient was not stable.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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