The Effect of Real Time Continuous Glucose Monitoring in Subjects With Pre-diabetes

Completed · Not applicable

Conditions studied: Pre-diabetes, Impaired Glucose Tolerance

In brief

This study will investigate whether real-time continuous glucose monitoring can be used as a tool for behavior change in people with pre-diabetes.

Key facts

Study ID

NCT01741467

Run by

Walter Reed National Military Medical Center

People needed

110

Starts

2012-05-01

Expected to finish

2016-08-01

Last updated by the study team

2016-10-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 or older
• Newly diagnosed with pre-diabetes (within the previous 6 months) with a FPG of > or = 110-125mg/dl or an A1c > or = 6% - 6.4%
• Able to independently measure and read finger stick blood glucose levels
• Willing to wear the CGM device for up to 12 weeks during the study period
• Willing to test blood sugar by fingerstick twice per day while wearing the CGM
• DEERS eligible

You may not qualify if…

• Using medication for pre-diabetes
• Women who are pregnant, lactating, planning to become pregnant, or without a safe contraceptive method; all female subjects will undergo pregnancy testing via a serum HcG with their initial blood testing.
• Subjects who are taking glucocorticoids, amphetamines, anabolic, or weight-reducing agents during the course of the study.
• Active Duty service members likely to be deployed during the 18-month study period.

Where it is running

• Walter Reed National Military Medical Center — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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