drugset / Trial / NCT00338104
Conversion of Hyperglycemic Patients Being Treated With Intravenous Insulin Infusions to Lantus Insulin
RandomizedParallel-groupOpen-labelTreatment
Summary
The primary objective of this study is to determine the optimal dose of glargine insulin when converting from intravenous short-acting continuous insulin infusions in surgical and intensive care unit patients using a prospective, controlled, parallel group, randomized study design. Note: Lantus insulin is the proprietary name for glargine insulin.
Timeline
- Start
- 2004-07
- Primary completion
- 2005-05
- Completion
- 2005-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | insulin glargine | Protein / enzyme biologic | 40 % | Subcutaneous |
| Subject | insulin glargine | Protein / enzyme biologic | 60 % | Subcutaneous |
| Subject | insulin glargine | Protein / enzyme biologic | 80 % | Subcutaneous |