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Clinical Trial Summary

The purpose of this study is to determine whether continuous glucose monitoring will improve glucose variability as measured by the coefficient of variation of glucose levels in very young children with T1D. The study adopts an open-label, multi-centre, multinational, prospective registry-based population cohort design contrasting CGM use to SMBG alone in young children with type 1 diabetes over 12 months. The primary endpoint is the difference between treatment modalities (CGM vs SMBG alone) in glycaemic variability, measured as the coefficient of variation of glucose levels, during the 12 months observational period. Other Key edpoints include time in range 70-180 mg/dl, time below range 70 mg/dl and time above range 180 mg/dl.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04558710
Study type Observational [Patient Registry]
Source University of Ljubljana, Faculty of Medicine
Contact
Status Completed
Phase
Start date June 1, 2018
Completion date December 30, 2019

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