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临床试验/NCT01655940
NCT01655940已完成不适用

Comparison of the FORE-SITE and INVOS Cerebral Oximeters During Cardiac Surgery

Nationwide Children's Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2011年5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
50
试验地点
1
主要终点
Oxygen saturation

研究概览

简要总结

In this prospective study to try to standardize the care for patients, the investigators are planning to compare two cerebral oximeters currently in use at NCH in terms of their accuracy in determining the cerebral oxygen saturation as determined by jugular bulb oxygen saturation. Also, the investigators will compare these devices in terms of their response to changes in hemodynamics that occur during cardiac surgery.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients undergoing cardiac surgery

排除标准

  • 未提供

结局指标

主要结局

Oxygen saturation

时间窗: during surgery - Day 1

cannulation, decannulation, hemodynamic instability

次要结局

  • Mean arterial pressure(during surgery - Day 1)

研究者

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

Aymen N Naguib

Director of Pediatric Cardiothoracic Anesthesia

Nationwide Children's Hospital

研究点 (1)

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