A Prospective Study With a New Device for the Monitoring of Cerebral Oxygenation on Cardiac Surgery Patients

Stopped early

Conditions studied: Coronary Artery Disease, Heart Valve Disease

In brief

The purpose of this study is to determine whether a new cerebral oxygenation monitoring device is comparatively similar to the current approved devices.

Key facts

Study ID

NCT00598936

Run by

University of California, Irvine

People needed

21

Starts

2007-11-01

Expected to finish

2009-05-01

Last updated by the study team

2011-09-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• To be 18 years old or older
• Scheduled for cardiac surgery
• Treatment will include 72 hours or more of hospital stay
• Understand enough about the risks and benefits of the study to be able to make an informed decision before agreeing to be in the study

You may not qualify if…

• History of cerebrovascular disease
• History of skin problems on forehead (skin rashes, acne, allergies, etc.)
• History of craniofacial surgeries
• Pregnancy

Where it is running

• University of California, Irvine Medical Center — Orange, California, United States

Full record on ClinicalTrials.gov

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