Clinical Trials Directory

Trials / Terminated

TerminatedNCT00464386

Continuous Glucose Monitoring (POC) in the ICU

Continuous Glucose Monitors (CGM) Versus Point-of-Care (POC) Glucometers in the Intensive Care Unit (ICU)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
23 (actual)
Sponsor
United States Army Institute of Surgical Research · Federal
Sex
All
Age
18 Years – 72 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to prospectively evaluate whether the addition of continuous glucose monitoring to point-of-care (POC) glucometer monitoring improves glucose control.

Detailed description

Severe burns and traumatic injury can be associated with protracted illness and prolonged ICU course. The beneficial effects of strict serum glucose control in critically ill surgical patients have been demonstrated. Continuous glucose monitors may improve glucose control by providing close to real-time glucose measurements, giving the critical care team the ability to react to trends before hypo- or hyperglycemia is reached. These improvements may decrease the morbidity and mortality associated with severe thermal injury, thereby minimizing hospital stay and recovery. Burned and injured soldiers, airmen, sailors, and marines may return to duty in a more expeditious fashion, or at minimum, enjoy a better quality of life after discharge from the intensive care unit.

Conditions

Interventions

TypeNameDescription
DEVICEContinuous Glucose Monitoringmeasure glucose levels on burn patients

Timeline

Start date
2006-09-01
Primary completion
2009-02-01
Completion
2013-12-01
First posted
2007-04-23
Last updated
2016-05-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00464386. Inclusion in this directory is not an endorsement.