Continuous Glucose Monitoring (CGM) in Subjects With Type 2 Diabetes

Inclusion Criteria:

- Have been diagnosed with type 2 diabetes mellitus

- Have an HgbA1c value ≥ 7% and ≤17%.

- Are on basal insulin, with or without oral agents

- Are not on basal bolus insulin therapy.

- Have had no severe hypoglycemic episodes in the 6 months prior to enrollment in the
study. Severe hypoglycemia will be defined as any hypoglycemia that is both
neurologically impairing and absolutely requires assistance from a third party in the
form of carbohydrates, glucagon shots, or attention from a paramedic or other
healthcare professional.

- Have no known allergy to medical tape or sensors.

- Are capable of and willing to test their blood glucose (BG) on an average of 4
times per day.

- Are willing to not use Acetaminophen while enrolled in the study.

- Are willing not to undergo a MRI procedure while wearing the CGM sensor.

- Are willing and capable of performing self insertions of the device sensor.

- Women of child bearing potential must be willing to use an approved form of birth
control while enrolled in the study.

- Women of child bearing potential must be willing to perform pregnancy tests monthly
while enrolled in the study.

- Can understand and speak English fluently.

Exclusion Criteria

- Have been on pump therapy in the 6 months prior to enrollment in the study.

- Are receiving basal- bolus insulin therapy

- Are taking any medication that is not approved to be taken with insulin.

- Are pregnant or have intentions of becoming pregnant during the duration of the
study.

- Have any skin condition that would inhibit the proper wearing of the CGM sensor
including severe psoriasis, burns, eczema, scarring, excessive tattoos, etc.

- Have a hematocrit ≤30% or ≥55%

- Are currently enrolled in another clinical study (subjects must have ended
participation in other studies at least 30 days prior to enrolling in this study.

- Are employed by any company that manufactures or is developing a CGM device.

- Are deemed incapable of participating in the study by the Primary Investigator for
any reason.