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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Division of Pediatric Endocrinology and Diabetes, Stanford University
Stanford, California, United States
Barbara Davis Center for Childhood Diabetes, University of Colorado
Denver, Colorado, United States
Department of Pediatrics, Yale University School of Medicine
New Haven, Connecticut, United States
Nemours Children's Clinic
Jacksonville, Florida, United States
Accuracy of the GlucoWatch G2 Biographer and CGMS sensors
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Jaeb Center for Health Research
Tampa, Florida, United States
Department of Pediatrics, University of Iowa Carver College of Medicine
Iowa City, Iowa, United States