Diabetes Type 1 Clinical Trial
Official title:
Feasibility Study to Assess Performance of an Integrated Sensor and Infusion Set. TRIAL II
The purpose of this study is to collect performance data on the integrated sensor and infusion set during 3 days of use and demonstrate performance adequacy of the Integrated sensor and infusion set with glucose sensing and insulin delivery functionalities. The hypothesis of this study is that having the infusion of insulin in close proximity to the sensor does not interfere with the sensor accuracy.
Sensor clinical accuracy will be evaluated based on the following parameters: Mean ARD
(absolute relative difference), median ARD, Clarke Grid Analysis. Meter BG values will be
used as reference. Descriptive statistics will be used to assess non-inferiority of the
Integrated sensor and infusion sets sensors compare to control Enlite sensors.
Insulin delivery functionality will be evaluated based on BG profiles obtained during
peri-prandial periods during which BG measurements will be performed at 15, 20, 30 min
intervals according to a SMBG schedule. Post-prandial pharmacodynamic profiles will be
analyzed to demonstrate the effect of insulin delivered using the Integrated sensor and
infusion set. Specifically, rise in glucose levels followed by their fall will be used as an
indication that insulin was delivered and absorbed. Post-prandial BG areas under the curve
(AUC), Tmax (time to maximum rise of BG), and Cmax (maximum post-prandial BG) values will be
calculated for each meal (breakfast, lunch, and dinner) consumed during both inpatient days
and compared. Intra - and inter-subject mean values and standard deviations will be
calculated. Paired and unpaired T-tests will be used to evaluate statistical significance.
Longevity of device performance will be assessed by comparing the listed parameters obtained
during two inpatient days.
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
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