NCT01394588

Brief Summary

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.

Trial Health

10
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2010

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

July 12, 2011

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 14, 2011

Completed
Last Updated

May 5, 2014

Status Verified

May 1, 2014

First QC Date

July 12, 2011

Last Update Submit

May 2, 2014

Conditions

Cardiac Surgery

Keywords

Cardiac SurgeryPerioperative Glucose Control

Study Arms (1)

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)

Interventions

Use of continuous glucose monitor during surgery. ( Medtronic Minimed Guardian REALTime Continuous Glucose Monitor)DEVICE

Use of continuous glucose monitor during surgery.

Also known as: Medtronic Minimed Guardian REALTime Continuous Glucose Monitor
Cardiac Surgery Patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Competent adults scheduled for elective cardiac surgery.

You may qualify if:

  • Competent adults scheduled for elective cardiac surgery.

You may not qualify if:

  • Inability to consent, emergency surgery.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Robert Schonberger, MD

    Yale University

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 12, 2011

First Posted

July 14, 2011

Study Start

August 1, 2010

Last Updated

May 5, 2014

Record last verified: 2014-05