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临床试验/NCT00606034
NCT00606034已完成4 期

A Prospective Trial of U500 Regular Insulin by Continuous Subcutaneous Insulin Infusion in Patients With Type 2 Diabetes and Severe Insulin Resistance Who Have Failed Previous Insulin Regimens

Mountain Diabetes and Endocrine Center1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2007年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
21
试验地点
1
主要终点
Improvement in Glycemic Control as Assessed by Change in Hemoglobin A1c (HbA1c)

研究概览

简要总结

Patients with Type 2 diabetes and severe insulin resistance with very large insulin requirements who have failed all previous insulin regimens using non-concentrated forms of insulin (U100 insulin formulations) will receive 5X concentrated insulin (U500 regular insulin)infused via insulin pump.

详细描述

Patients with Type 2 diabetes who have severe insulin resistance and very large insulin requirements (over 1.4 units of insulin /kg/day) often fail insulin regimens with persistent poor blood glucose control when standard U-100 insulin formulations are used. This is due in part to poor absorption of the large insulin volumes required using these less concentrated standard insulin preparations. The hypothesis that using a concentrated form of insulin called U-500 Regular insulin and delivering it by infusion via insulin pump will lower the volume of insulin required and therefore improve insulin absorption, which will lead to improved blood glucose control, will be tested.

研究设计

研究类型
Interventional
分配方式
Non Randomized
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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Type 2 diabetes on stable insulin regimen with or without oral agents for at least 3 months
  • HbA1c > 7%
  • No significant cardiovascular, renal or other serious medical diseases

排除标准

  • HbA1c < 7%
  • Chronic renal, hepatic, cardiovascular, or other serious medical illness
  • Females of childbearing age not using adequate contraception
  • Use of GLP mimetic

研究组 & 干预措施

All subjects active

Experimental

All subjects will receive the experimental treatment (U-500 insulin via Omnipod) since they have already failed all other previous insulin treatment regimens.

干预措施: U-500 Insulin delivered by Omnipod (disposable insulin pump) (Drug)

结局指标

主要结局

Improvement in Glycemic Control as Assessed by Change in Hemoglobin A1c (HbA1c)

时间窗: 1 year

HbA1c is expressed as a percentage. This measurement represents an average of plasma glucose concentration for about 3 months. We will report the change in HbA1c measured at 12 months vs Baseline.

次要结局

  • Percentage of Time Spent in Hypoglycemia(baseline versus 12 months)
  • Patient Satisfaction With Insulin Delivery Method Via Insulin Delivery Rating System Questionnaire (IDRSQ)(Baseline versus 1 year)

研究者

发起方
Mountain Diabetes and Endocrine Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Wendy Lane MD

Director of Research, Principal Investigator

Mountain Diabetes and Endocrine Center

研究点 (1)

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