The objective of this study is to generate preliminary data in an inpatient setting to help optimize an insulin dosing logic (that decides how much to deliver insulin) for Eli Lilly's system.
After being informed about the study and potential risks, all participants giving written informed consent will undergo an admission visit to determine eligibility for study entry. Participants who meet the inclusion and exclusion criteria will then participate in two 41-hour intervention visits using Eli Lilly's insulin dosing algorithm.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
41-hour intervention period in which the participants are treated with rapid insulin in the closed-loop system.
Centre for Innovative Medicine at McGill University Health Centre Research Institute
Montreal, Quebec, Canada
Glucose outcomes: percentage of time spent in specific glucose ranges (ex: 3.9-10.0 mmol/L)
As this is a pilot study, the only primary outcome is the glucose outcomes during the closed-loop portion.
Time frame: 24 hours
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