Diabetes Mellitus Clinical Trial
Official title:
DirecNet Pilot Study to Assess the Accuracy of Continuous Glucose Monitors in Normal Children
Continuous glucose monitors may be useful in the treatment of children with Type 1 diabetes mellitus. The purpose of this study was to determine whether two FDA-approved continuous glucose monitors, the Continuous Glucose Monitoring System (CGMS) and the GlucoWatch G2TM Biographer (GW2B), are sufficiently accurate to use in future studies to characterize glucose levels in children.
The characterization of glucose levels in healthy children during day and nighttime is
critical to the interpretation of glucose levels in diseases such as diabetes. This study
was conducted by the DirecNet Study Group to determine whether two FDA-approved continuous
glucose monitors are sufficiently accurate.
The study was conducted at five clinical centers and enrolled approximately 20 healthy
children (ages 7 to 17 years old) who did not have Type 1 or Type 2 diabetes nor a history
of the disease in their immediate families. Each participant was hospitalized for
approximately 26 hours to assess the accuracy of the continuous glucose monitors compared
with serum glucose determinations.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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