Effectiveness and Safety of the Dexcom™ G4 Continuous Glucose Monitoring System in Pediatric Subjects With Diabetes Mellitus

Status:	Recruiting
Conditions:	Diabetes
Therapuetic Areas:	Endocrinology
Healthy:	No
Age Range:	Any
Updated:	2/4/2013
Start Date:	July 2012

Effectiveness and Safety of the Dexcom™ G4 Continuous Glucose Monitoring System in Pediatric Subjects With Diabetes Mellitus.

The primary objective of the study is to evaluate the safety and effectiveness of the G4
System (System) when used as an adjuvant to blood glucose testing over a 7-day period in
pediatric subjects with diabetes mellitus.

System effectiveness will be primarily evaluated with comparison to laboratory reference
Yellow Springs Instrument (YSI) venous sample measurements. The system performance will be
evaluated in terms of point and rate accuracy of the system in reference to YSI. The point
accuracy is measured as the proportion of G4 System values that are within ±20% of YSI
reference value for glucose levels >80 mg/dL and ±20 mg/dL at YSI glucose levels <80 mg/dL.
The trend accuracy of the device performance, i.e., continuous glucose error grid analysis,
will be evaluated as well as the temporal accuracy at different glucose rates of changes and
different glucose ranges (hypoglycemic, euglycemic, and hyperglycemic ranges). The primary
matched paired (Sensor-YSI) measurements will be collected during one in-clinic session.
System effectiveness will also be evaluated with SMBG measurements similarly.

Safety data of the system will also be collected and safety will be characterized by the
incidence of Adverse Device Effects (ADE) experienced by study participants.

Other objectives include the evaluation of device performance at an alternate site (the
upper buttocks).

Inclusion Criteria:

- Ages 2 to 17 years ;

- Diagnosis of diabetes mellitus;

- Willing to participate in one 7-day Sensor wear period;

- Willing to wear 2 systems simultaneously;

- Willing to take a minimum of 7 fingersticks per day during home use with a blood
glucose meter provided;

- Willing to attend one in-clinic session of up to 6 hours duration. Clinic procedures
where blood sampling via SMBG and/or venous YSI method, depending on age;

- Subject or guardian is able to speak, read, and write English.

Exclusion Criteria:

- Extensive skin changes/diseases at sensor wear site that preclude wearing the Sensor
on normal skin (e.g. extensive psoriasis, recent burns or severe sunburn, extensive
eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis);

- Known allergy to medical-grade adhesives;

- Require a magnetic resonance imaging (MRI) scan, computed tomography (CT) scan, or
diathermy during the wear period. If any of these procedures are required urgently
during the study, subjects will notify the study staff, end their continuous glucose
monitoring (CGM) session, and remove their sensor.

We found this trial at

sites

Rocky Mountain Diabetes and Osteoporosis Center

Idaho Falls, Idaho 83404

from

Idaho Falls, ID