跳至主要内容
临床试验/NCT01186003
NCT01186003已完成不适用

Effectiveness of a Subcutaneously Administered Long-Acting Insulin Detemir Added to Insulin Drip Therapy as Compared With Standard Insulin Drip Treatment

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2010年8月最近更新:
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
30
试验地点
1
主要终点
Reduction in Rebound Hyperglycemia (Blood Glucose Levels Over 180 mg/dl)

研究概览

简要总结

The investigators anticipate that the use of Detemir will decrease the duration of an insulin drip, the dose of short-acting insulin in the drip, hospital and ICU (intensive care unit) length of stay, improve glycemic control, and prevent rebound hyperglycemias when the insulin drip is discontinued.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diabetic ketoacidosis (DKA) and hyperosmolar non-ketotic states, hyperglycemia with severe illness, pre-and postoperative states, nothing by mouth (NPO), as well as gastric (tube feeding) and parenteral nutritional requiring insulin drip.
  • Patients with type 1 and type 2 diabetes mellitus (DM) will be included.
  • Patient with both types of diabetes will be among those treated with insulin drip while being NPO, having severe concomitant illness or receiving enteral and parenteral nutrition
  • Patients will be of age 19 to 80.

排除标准

  • Inability to consent for the study for any reason including cognitive impairment secondary to hyperglycemia, presence of severe medical conditions requiring intubation, severe sepsis, hypothermia, and anticipated length of insulin drop 2 weeks and longer, pregnancy, Levemir allergy, and concurrent sulfonamide treatment

研究组 & 干预措施

Insulin drip and Detemir

Active Comparator

Detemir 0.25 units per kg body weight given subcutaneously every 24 hours while patients are receiving intravenous (IV) standard insulin drip therapy

干预措施: Detemir (Drug)

结局指标

主要结局

Reduction in Rebound Hyperglycemia (Blood Glucose Levels Over 180 mg/dl)

时间窗: within 48 hours of discontinuation

Number of participants exhibiting rebound hyperglycemia (blood glucose levels over 180 mg/dl)

次要结局

  • Reduction in Duration of Insulin Drip Therapy and Reduction in Total and Average Per Hour Insulin Drip Dose(within one week of insulin drip therapy)
  • Reduction in ICU Length of Stay(within two weeks of hospitalization)
  • Equal or Improved Diabetes Control(within two weeks of hospitalization)
  • Reduction in Time to Get Back to Control of Glycemia (140-180 mg/dl) if Rebound Hyperglycemia Occurs(within one week post insulin drip)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Effectiveness of Adding Subcutaneous Long-Acting... | 临床试验