Continuous Glucose Monitoring Technology in the Perioperative Period During Cardiac Surgery
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|ClinicalTrials.gov Identifier: NCT01394588|
Recruitment Status : Withdrawn (On further investigation, it was found that the continuous glucose monitors required a calibration period that precluded reliable data collection.)
First Posted : July 14, 2011
Last Update Posted : May 5, 2014
|Condition or disease||Intervention/treatment|
|Cardiac Surgery||Device: Use of continuous glucose monitor during surgery. ( Medtronic Minimed Guardian REALTime Continuous Glucose Monitor)|
|Study Type :||Observational|
|Actual Enrollment :||0 participants|
|Official Title:||A Prospective Observational Trial of Continuous Glucose Monitoring Technology in the Perioperative Period During Cardiac Surgery|
|Study Start Date :||August 2010|
Cardiac Surgery Patients
Competent Adult Patients going for elective cardiac surgery.
Device: Use of continuous glucose monitor during surgery. ( Medtronic Minimed Guardian REALTime Continuous Glucose Monitor)
Use of continuous glucose monitor during surgery.
Other Name: Medtronic Minimed Guardian REALTime Continuous Glucose Monitor
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01394588
|Principal Investigator:||Robert Schonberger, MD||Yale University|