A Study of an Automated Insulin Delivery System in Adult Participants With Type 1 Diabetes Mellitus

Completed · Not applicable

Conditions studied: Type 1 Diabetes Mellitus

In brief

The purpose of this study is to evaluate whether an Automated Insulin Delivery (AID) System is safe to use and functions as intended with personalized basal insulin rates and when basal insulin rates are increased.

Key facts

Study ID

NCT03849612

Run by

Eli Lilly and Company

People needed

10

Starts

2019-02-21

Expected to finish

2019-03-27

Last updated by the study team

2019-04-25

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants with T1DM for at least 2 years and who have used an insulin delivery system with any rapid-acting insulin analog for the preceding 6 months
• Have a body mass index of 18.5 to 37 kilogram per meter squared
• Have a hemoglobin A1c level ≥6.0% and ≤9.0%

You may not qualify if…

• Have known allergies or history of hypersensitivity to insulin lispro
• Have had an episode of severe hypoglycemia within the past 6 months
• Have had more than 1 episode of diabetic ketoacidosis in the past 6 months

Where it is running

• Diablo Clinical Research — Walnut Creek, California, United States

Full record on ClinicalTrials.gov

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