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| Sponsors and Collaborators: |
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Information provided by: | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| ClinicalTrials.gov Identifier: | NCT00069537 |
Purpose
Good control of blood glucose levels is important in preventing complications from diabetes. This study assessed the accuracy and reliability of two FDA-approved continuous glucose monitors, the Continuous Glucose Monitoring System (CGMS) and the GlucoWatch G2 Biographer (GW2B), in children with type 1 diabetes mellitus (T1DM).
| Condition | Intervention | Phase |
|
Diabetes Mellitus, Insulin-Dependent |
Device: The GlucoWatch® G2™ Biographer (GW2B) Device: The Continuous Glucose Monitoring System (CGMS™) |
Phase IV |
| MedlinePlus related topics: | Diabetes Diabetes Type 1 |
| Drug Information available for: | Insulin Dextrose |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | DirecNet Inpatient Study to Test the Accuracy of Continuous Blood Glucose Monitoring Devices in Children With Type 1 Diabetes |
| Estimated Enrollment: | 90 |
| Study Start Date: | May 2002 |
| Estimated Study Completion Date: | November 2002 |
Intensive control of blood glucose levels has been shown to substantially prevent or delay complications of T1DM in adolescents and adults. The major limitation to implementation of intensive glycemic control is hypoglycemia. Younger children may be at increased risk for hypoglycemia and the risk/benefit ratio of intensive glycemic control may be less favorable in this population. Intensive therapy has not been systematically evaluated in children less than 13 years of age. This study was conducted by the Diabetes Research in Children Network (DirecNet) to assess the accuracy of the CGMS and the GW2B glucose monitors in comparison with standard blood glucose measurements in an inpatient setting.
During 24-hour clinical research center stays at five clinical centers, approximately 90 children and adolescents with T1DM (1 to 17 years of age) wore two FDA-approved continuous glucose monitors, CGMS and GW2B, and had frequent serum glucose determinations during the day and night. To assess glucose monitor function during periods of rising and falling blood glucose, insulin-induced hypoglycemia and meal-induced hyperglycemia tests were also performed.
Eligibility
| Ages Eligible for Study: | 1 Year to 17 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Exclusion Criteria
Contacts and Locations| United States, California | |||||
| Division of Pediatric Endocrinology and Diabetes, Stanford University | |||||
| Stanford, California, United States, 94305-5208 | |||||
| United States, Colorado | |||||
| Barbara Davis Center for Childhood Diabetes, University of Colorado | |||||
| Denver, Colorado, United States, 80262 | |||||
| United States, Connecticut | |||||
| Department of Pediatrics, Yale University School of Medicine | |||||
| New Haven, Connecticut, United States, 06519 | |||||
| United States, Florida | |||||
| Jaeb Center for Health Research | |||||
| Tampa, Florida, United States, 33647 | |||||
| Nemours Children’s Clinic | |||||
| Jacksonville, Florida, United States, 32207 | |||||
| United States, Iowa | |||||
| Department of Pediatrics, University of Iowa Carver College of Medicine | |||||
| Iowa City, Iowa, United States, 52242 | |||||
| Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Study Chair: | William V. Tamborlane, MD | Yale University |
More Information
| Study ID Numbers: | DirecNet 001, HD041890, HD041919-01, HD041908-01, HD041906-01, HD041918-01, HD041915 |
| First Received: | September 29, 2003 |
| Last Updated: | September 21, 2005 |
| ClinicalTrials.gov Identifier: | NCT00069537 |
| Health Authority: | United States: Federal Government |
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