Overview

Effectiveness of Adding Subcutaneous Long-Acting Detemir to Insulin Drip Therapy Compared With Standard Insulin Drip Therapy

Status:
Completed
Trial end date:
2017-10-01
Target enrollment:
0
Participant gender:
All
Summary
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.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Colorado, Denver
Collaborator:
Novo Nordisk A/S
Treatments:
Insulin
Insulin Detemir
Insulin, Globin Zinc
Criteria
Inclusion Criteria:

- 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.

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 drop 2 weeks
and longer, pregnancy, Levemir allergy, and concurrent sulfonamide treatment