Continuous Glucose Monitoring Technology in the Perioperative Period During Cardiac Surgery
This study is currently recruiting participants.
Verified July 2011 by Yale University
Sponsor:
Yale University
Collaborators:
Medtronic
Information provided by:
Yale University
ClinicalTrials.gov Identifier:
NCT01394588
First received: July 12, 2011
Last updated: July 13, 2011
Last verified: July 2011
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Purpose
This is an observational study of continuous glucose monitoring technology during cardiac surgery. The investigators would like to develop data for descriptive analysis of a comparison of continuous glucose monitoring with a gold standard under the conditions of cardiac surgery.
| Condition | Intervention |
|---|---|
|
Cardiac Surgery |
Device: Use of continuous glucose monitor during surgery. ( Medtronic Minimed Guardian REALTime Continuous Glucose Monitor) |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | A Prospective Observational Trial of Continuous Glucose Monitoring Technology in the Perioperative Period During Cardiac Surgery |
Resource links provided by NLM:
MedlinePlus related topics:
Heart Surgery
Drug Information available for:
Dextrose
U.S. FDA Resources
Further study details as provided by Yale University:
| Estimated Enrollment: | 50 |
| Study Start Date: | August 2010 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
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
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Competent adults scheduled for elective cardiac surgery.
Criteria
Inclusion Criteria:
- Competent adults scheduled for elective cardiac surgery.
Exclusion Criteria:
- Inability to consent, emergency surgery.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01394588
Contacts
| Contact: Robert Schonberger, MD | 2037852802 | robert.schonberger@yale.edu |
Locations
| United States, Connecticut | |
| Yale New Haven Hospital | Recruiting |
| New Haven, Connecticut, United States, 06510 | |
Sponsors and Collaborators
Yale University
Medtronic
Investigators
| Principal Investigator: | Robert Schonberger, MD | Yale University |
More Information
No publications provided
| Responsible Party: | Robert Schonberger, Yale University |
| ClinicalTrials.gov Identifier: | NCT01394588 History of Changes |
| Other Study ID Numbers: | 1006006996 |
| Study First Received: | July 12, 2011 |
| Last Updated: | July 13, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Yale University:
|
Cardiac Surgery Perioperative Glucose Control |
ClinicalTrials.gov processed this record on May 23, 2013