Effectiveness of Adding Subcutaneous Long-acting Glargine to Insulin Drip Therapy Compared With Standard Insulin Drip Therapy
| Status: | Completed |
|---|---|
| Conditions: | Diabetes |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 9/23/2012 |
| Start Date: | April 2010 |
| End Date: | April 2011 |
| Contact: | Karen J Gray, BS |
| Email: | karen.gray@ucdenver.edu |
| Phone: | 720-848-2679 |
Effectiveness of a Subcutaneously Administered Long-acting Insulin Added to Insulin Drip Therapy as Compared With Standard Insulin Drip Treatment
The investigators anticipate that the use of Glargine 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.
Inclusion Criteria:
- Diabetic ketoacidosis (DKA) and hyperglycemic hyperosmolar non-ketotic states,
hyperglycemia with severe illness, pre- and postoperative states, nothing by mouth
(NPO), as well as gastric (tube feeding) and parenteral nutrition requiring insulin
drip.
- Patients with type 1 and type 2 diabetes mellitus (DM) will be included.
- Patients with both types of diabetes will be among those treated with the insulin
drip while being NPO, having severe concomitant illness or receiving enteral and
parenteral nutrition.
- Patients will be of age 19 to 80.
Exclusion Criteria:
- 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 drip 2
weeks and longer, pregnancy, Lantus allergy, and concurrent sulfonamide treatment
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