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临床试验/NCT01484457
NCT01484457已完成早期 1 期

Controlled Insulin Delivery: Combining Technology With Treatment

Sansum Diabetes Research Institute3 个研究点 分布在 2 个国家目标入组 19 人开始时间: 2008年7月最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
19
试验地点
3
主要终点
Restoration of Euglycemia

研究概览

简要总结

Hypothesis: Closed-loop control systems for an artificial pancreas using multi-parametric model predictive control can be developed and evaluated safely in patients with Type 1 Diabetes Mellitus (T1DM) to control blood glucose concentrations.

This study seeks to combine real-time continuous glucose sensing with automated insulin delivery in a closed-loop system that will achieve euglycemia in patients with T1DM. The end result of this line of research will be an artificial pancreas that will provide around-the-clock glucose regulation through controlled insulin delivery in response to detected patterns of change in glucose levels.

详细描述

The goal of the JDRF Artificial Pancreas Project is to produce an autonomous artificial pancreas that can safely and effectively regulate glycemia in people with type 1 diabetes mellitus. In our work, this fully automated closed-loop system combines a subcutaneous continuous glucose monitor (CGM) and a continuous subcutaneous insulin infusion (CSII) pump with a sophisticated control algorithm. This is a proof-of-concept study to demonstrate that the controller could bring the patient back to a relatively normal glucose concentration after an unannounced meal and from mild hyperglycemia. Once the system is initiated, all insulin delivery is calculated automatically. There was no outside intervention either by the subject or medical personnel. An artificial pancreas system that aims at replicating normal beta-cell function by using the subcutaneous-subcutaneous (sc-sc) route needs to address inherent delays in both glucose sensing and insulin delivery. Our strategic approach is that a closed-loop system should operate safely without any knowledge of meals or other disturbances. We have developed the Artificial Pancreas System (APS©) and used it to clinically evaluate a control strategy that allows efficient glycemic control without any a priori meal information. The Artificial Pancreas device uses the Artificial Pancreas System (APS©) platform with the OmniPod insulin pump, the DexCom SEVEN PLUS CGM and a multi-parametric model predictive control algorithm (mpMPC) with an insulin-on-board (IOB) safety constraint.

研究设计

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

入排标准

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

入选标准

  • Willing to sign the consent form
  • Type 1 diabetes for at least 1 year prior to the study
  • Using continuous subcutaneous insulin infusion pump
  • Above 21 years of age
  • Willing to follow the study requirements

排除标准

  • Allergy to the sensor or to one of its components
  • Psychiatric disorders
  • Reported diabetic ketoacidosis within last 3 months
  • Abnormal liver function (Transaminase > 2 times the upper limit of normal)
  • Heart failure
  • Any carcinogenic disease
  • Any other chronic abnormality
  • Unwilling to perform or to follow the research protocol
  • Participation in any other study concurrent with the proposed study
  • Creatinine concentration above the upper limit of normal for age and sex
  • Active coronary artery disease
  • Active gastroparesis
  • History of uncontrolled seizures
  • Untreated adrenal insufficiency
  • Hypokalemia
  • Uncontrolled thyroid disease.
  • Condition, which in the opinion of the investigator, would interfere with patient safety

结局指标

主要结局

Restoration of Euglycemia

时间窗: 12 hours

The primary endpoint of this pilot study is successful restoration of euglycemia from the two perturbed conditions using closed loop control with minimal hypo- and hyperglycemia exposure. The first condition involves restoration of euglycemia when the subject is in a hyperglycemic state. The second condition involves restoration of euglycemia following consumption of a meal containing 25g CHO with no insulin bolus. The patients will be followed for the duration of the 12 hour study.

次要结局

  • Average percent-of-time-in-range (80 - 180 mg/dL)(12 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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