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The purpose of this study is to determine whether a new cerebral oxygenation monitoring device is comparatively similar to the current approved devices.
Cerebral oxygenation monitoring is an innovative way to monitoring cardiac surgery patients intraoperatively to reduce the incidence of postoperative hypoxic side effects. There are a number of approved devices already in the market that have proved their efficacy.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of California, Irvine Medical Center
Orange, California, United States
Start Date
November 1, 2007
Primary Completion Date
May 1, 2009
Completion Date
May 1, 2009
Last Updated
September 5, 2011
21
ACTUAL participants
CDI 1000 COM and INVOS 5100
DEVICE
Lead Sponsor
University of California, Irvine
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05208567