drugset / Trial / NCT00338104

Conversion of Hyperglycemic Patients Being Treated With Intravenous Insulin Infusions to Lantus Insulin

NCT00338104 ↗

Phase 4 Completed 75 enrolled Northwestern University Sanofi · collab
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

EvaluationDrugModalityDoseRoute
Subject insulin glargine Protein / enzyme biologic 40 % Subcutaneous
Subject insulin glargine Protein / enzyme biologic 60 % Subcutaneous
Subject insulin glargine Protein / enzyme biologic 80 % Subcutaneous