This study is conducted in Europe. The aim of this observational study is to evaluate the blood glucose control when using NovoMix® 50 up to 12 months after initiation subjects with type 2 diabetes currently on a therapy with human biphasic insulin. An additional objective is also to observe the different regimes of starting and maintaining the treatment with NovoMix® 50 during one year.
Study Type
OBSERVATIONAL
Enrollment
270
Efficacy and safety data collection in connection with the use of the drug NovoMix® 50 in daily clinical practice.
Novo Nordisk Investigational Site
Ljubljana, Slovenia
Change in HbA1c
Time frame: At 0, 3, 6, 9, 12 months
Percentage of subjects achieving target HbA1c
Time frame: At 0, 3, 6, 9, 12 months
Change in FPG (fasting plasma glucose)
Time frame: At 0, 3, 6, 9, 12 months
Change in PPG (postprandial glucose)
Time frame: At 0, 3, 6, 9, 12 months
Change in number of hypoglycaemic events
Time frame: At 0, 3, 6, 9, 12 months
Change in insulin presentation
Time frame: At 0, 3, 6, 9, 12 months
Dose and number of injections
Time frame: At 0, 3, 6, 9, 12 months
Number of ADRs (adverse drug reaction)
Time frame: At 0, 3, 6, 9, 12 months
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