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临床试验/NCT03848767
NCT03848767已完成不适用

An Early Feasibility Study to Evaluate the Functionality and Safety of an Automated Insulin Delivery System in Adult Patients With Type 1 Diabetes Mellitus During Meal Challenges

Eli Lilly and Company1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2019年2月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Continuous Glucose Monitor (CGM) Measured Percentage of Time <70 mg/dL

研究概览

简要总结

The Automated Insulin Delivery (AID) System is an investigational insulin delivery device being developed for use for participants with diabetes. The purpose of this study is to assess the safety of the AID system during meal challenges.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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%

排除标准

  • 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

研究组 & 干预措施

AID System Containing Insulin Lispro

Experimental

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.

干预措施: AID System (Device)

AID System Containing Insulin Lispro

Experimental

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.

干预措施: Insulin Lispro (Drug)

结局指标

主要结局

Continuous Glucose Monitor (CGM) Measured Percentage of Time <70 mg/dL

时间窗: In-Patient Period (3 Days)

CGM measured percentage of time \<70 milligrams per deciliter (mg/dL)

Number of Adverse Events (AEs)

时间窗: In-Patient Period (3 Days)

Number of AEs

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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