Continuous Glucose Monitoring (POC) in the ICU

Stopped early · Not applicable

Conditions studied: Burns, Trauma

In brief

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.

Key facts

Study ID

NCT00464386

Run by

United States Army Institute of Surgical Research

People needed

23

Starts

2006-09-01

Expected to finish

2013-12-01

Last updated by the study team

2016-05-02

Who can join

Age: 18 and older, up to 72. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• remain 1 week in an ICU
• 18-72 years old
• severe trauma or thermal injury greater than 20% TBSA burn

You may not qualify if…

• cerebral arterial injury
• myocardial infarction
• pre-existing renal failure or liver failure
• history of hypoglycemia
• history or high risk of seizures
• pregnancy

Where it is running

• US Army Institute of Surgical Research — Fort Sam Houston, Texas, United States

Full record on ClinicalTrials.gov

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