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Continuous Glucose Monitoring in Critically Ill Surgical Patients

NCT01108640 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2014-06-16

No results posted yet for this study

Summary

The specific aim of this study is to identify the degree of correlation between real time subcutaneous glucose monitoring and intermittent glucose monitoring using capillary glucose samples, arterial blood samples and venous blood samples in critically ill surgical patients. A secondary aim will be to determine the accuracy of real time glucose monitoring.

Conditions

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Yale University

    lead OTHER

Principal Investigators

  • Kevin M Schuster, MD · Yale University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2012-07-31
Completion
2012-07-31

Countries

  • United States

Study Locations

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Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01108640 on ClinicalTrials.gov