Continuous Glucose Monitoring in Critically Ill
Stopped early · Not applicable
Conditions studied: Diabetes
In brief
The goal of this clinical research study is to learn if The Guardian® blood-sugar monitoring device can be used reliably in patients with high blood sugar who are receiving care in the ICU. Researchers will compare blood-sugar measurements from the study device with blood-sugar measurements from the standard "fingerstick" method of blood-sugar testing. This is being done to see if the new device can accurately measure blood sugar.
Key facts
- Study ID
- NCT00707434
- Run by
- M.D. Anderson Cancer Center
- People needed
- 6
- Starts
- 2008-06-01
- Expected to finish
- 2016-09-01
- Last updated by the study team
- 2020-03-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients in any of our University of Texas collaborative intensive care units.
- Critically ill patients on an insulin infusion protocol
You may not qualify if…
- Patients or their legal representatives who do not consent
- Patients with large areas of skin affected so as not to allow implantation of device.
- Patients < 18 years of age
Where it is running
- The University of Texas Southwestern Medical Center at Dallas — Dallas, Texas, United States
- University of Texas Medical Branch at Galveston — Galveston, Texas, United States
- University of Texas Health Science Center at Houston — Houston, Texas, United States
- University of Texas MD Anderson Cancer Center — Houston, Texas, United States
- University of Texas Health Science Center at San Antonio — San Antonio, Texas, United States
- University of Texas Health Science Center at Tyler — Tyler, Texas, United States
Full record on ClinicalTrials.gov
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