Diabetes Mellitus, Type 2
Conditions
Keywords
Insulin pump therapy, Eli Lilly
Brief summary
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.
Detailed description
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.
Interventions
OTHERInsulin closed-loop
41-hour intervention period in which the participants are treated with rapid insulin in the closed-loop system.
Sponsors
McGill University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
To be eligible for the study, all participants must meet the following criteria: 1. Adult male or female ≥ 18 years of age. 2. Type 2 diabetes mellitus has been clinically diagnosed (the diagnosis of type 2 diabetes is based on the investigator's judgment) for at least 12 months 3. Using multiple daily insulin injections (one basal and ≥ 2 prandial doses) for ≥ 3 months. 4. Using insulin glargine (U100 or U300), detemir, degludec, or NPH. 5. Most recent (in the last 6 month) HbA1c ≤ 10%. 6. Use of a GLP1 agonist or SGLT inhibitor for the past 3 months.
Exclusion criteria
Participants who meet any of the following criteria are not eligible for the study: 1. Severe hypoglycaemic episode ≤ two months before admission. 2. Ongoing pregnancy, or any newly diagnosed pregnancy throughout the study 3. Clinically significant nephropathy, neuropathy or retinopathy as judged by the investigator. 4. Recent (within the past 6 months) acute macrovascular event (e.g. acute coronary syndrome or cardiac surgery). 5. Peripheral vascular disease, foot ulcer, Charcot arthropathy or any condition that limits ability to walk 6. Other serious medical illness likely to interfere with study participation or with the ability to complete the trial by the judgment of the investigator. 7. Use of oral hypoglycaemic agents besides SGLTi's, GLP1 agonists, and or metformin and unwilling to discontinue for the run-in and intervention period.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Glucose outcomes: percentage of time spent in specific glucose ranges (ex: 3.9-10.0 mmol/L) | 24 hours | As this is a pilot study, the only primary outcome is the glucose outcomes during the closed-loop portion. |
Countries
Canada
Outcome results
None listed