Primary Objective: \- To evaluate the decrease of Hb A1c ≥ 1% after 6 month treatment in patients with Type 2 Diabetes Mellitus (T2DM) uncontrolled on Oral Antidiabetics (OADs) Secondary Objectives: * To evaluate the percentage of patients with Hb A1c \< 7.5%, * To evaluate the rate of hypoglycaemia (symptomatic, severe) * To evaluate the middle dose of insulin per product - Insuman Basal, Insuman Comb, Insuman Rapid after 6 month treatment * To evaluate the change in Fasting Plasma Glucose (FPG) after 6 month treatment * To assess the overall safety * To evaluate the efficacy of education courses in Diabetes Schools (% of correct answers after second test compare to the testing of the initial level)
6 months
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
552
Pharmaceutical form: solution for injection Route of administration: subcutaneous
Sanofi-Aventis Administrative Office
Kyiv, Ukraine
Decrease of Hb A1c ≥ 1%
Time frame: Baseline, 6 months
Percentage of patients with Hb A1c < 7.5%
Time frame: 6 months
Rate of hypoglycaemias (symptomatic, severe)
Time frame: 6 months
Middle dose of insulin per product (Insuman Basal, Insuman Comb, Insuman Rapid)
Time frame: 6 months
Change in FPG
Time frame: Baseline 6 months
Number of patients with adverse events
Time frame: 6 months
Assessment of efficacy of education courses in Diabetes Schools
Percentage of correct answers after second test compare to the testing of the initial level
Time frame: Baseline, 6 months
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