Status:
TERMINATED
Effects of Cerebral Oxygen Saturation on Neuropsychological Outcomes
Lead Sponsor:
Weill Medical College of Cornell University
Collaborating Sponsors:
New York Presbyterian Hospital
Conditions:
Cardiovascular Diseases
Postoperative Complications
Eligibility:
All Genders
18-80 years
Phase:
PHASE2
PHASE3
Brief Summary
The purpose of this study is to evaluate the effects of maintaining adequate cerebral oxygen saturation (over 40%) on patients undergoing cardiac surgery. Effects on neuropsychological outcome, length...
Detailed Description
Central nervous system dysfunction is a major cause of morbidity after cardiac surgery. This study seeks to evaluate the effects of cerebral oxygen saturation on the neuropsychological outcome of card...
Eligibility Criteria
Inclusion
- Adult patient
- Elective cardiac surgery with cardiopulmonary bypass
- Coronary artery disease or valvular heart disease or combination of both
- Ability and willingness to give informed consent
Exclusion
- Pediatric patients
- Emergency surgery
- Unable to understand English
- Allergic to tape used to attach oxygen sensor
Key Trial Info
Start Date :
February 1 2001
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2007
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT00151307
Start Date
February 1 2001
End Date
April 1 2007
Last Update
June 6 2008
Active Locations (1)
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1
New York Presbyterian Hospital, Weill Medical College of Cornell University
New York, New York, United States, 10021