A Study of an Automated Insulin Delivery System in Adult Participants With Type 1 Diabetes Mellitus During Meal Challenges
NCT ID: NCT03848767
Last Updated: 2019-04-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2019-02-20
2019-04-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DEVICE_FEASIBILITY
NONE
Study Groups
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AID System Containing Insulin Lispro
The AID system is comprised of a continuous subcutaneous insulin infusion (CSII) pump component with a hybrid closed-loop control (HCLC) algorithm, and a continuous glucose monitor (CGM) component.
AID System
AID System
Insulin Lispro
Individualized doses of insulin lispro administered via the AID system to maintain glycemic control except during meal challenges.
Interventions
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AID System
AID System
Insulin Lispro
Individualized doses of insulin lispro administered via the AID system to maintain glycemic control except during meal challenges.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Have a body mass index of 18.5 to 37 kilogram per meter squared
* Have a hemoglobin A1c level ≥6.0% and ≤9.0%
Exclusion Criteria
* 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
18 Years
65 Years
ALL
No
Sponsors
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Eli Lilly and Company
INDUSTRY
Responsible Party
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Principal Investigators
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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Role: STUDY_DIRECTOR
Eli Lilly and Company
Locations
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Rainier Clinical Research Center
Renton, Washington, United States
Countries
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Other Identifiers
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F3Z-MC-IORD
Identifier Type: OTHER
Identifier Source: secondary_id
17177
Identifier Type: -
Identifier Source: org_study_id
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