NPH and Regular Insulin in the Treatment of Inpatient Hyperglycemia: Comparison of 3 Basal-bolus Regimens
Diabetes Mellitus, Hyperglycemia
About this trial
This is an interventional treatment trial for Diabetes Mellitus focused on measuring Diabetes Mellitus, Hospital Hyperglycemia
Eligibility Criteria
Inclusion Criteria:
- Admitted to medical services
- Persistent blood glucose level > 140 mg/dL
- With an expected stay ≥ 48 hours
Exclusion Criteria:
- Subjects with type 1 diabetes mellitus
- Parenteral nutrition
- Glucose levels ≥ 400 mg/dL at screening
- Diabetic ketoacidosis or non-ketosis hyperosmolar state
- Clinically relevant hepatic disease
- Glomerular filtration rate ≤ 30 ml/min
- Pregnancy
- Terminal disease
- Inability to provide informed consent
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Once-daily insulin
Twice-daily insulin
Triple-daily insulin
60% of total dose of insulin as NPH insulin in the once-daily regimen was administered subcutaneously before breakfast. Also, 40% in rapid insulin before meals (every 8 hours).
60% of total dose of insulin as NPH insulin in the twice-daily regimen it was given before breakfast and before dinner. Also, 40% in rapid insulin before meals (every 8 hours).
60% of total dose of insulin as NPH insulin in the triple daily regimen it was administered before each meal. Also, 40% in rapid insulin before meals (every 8 hours).