This trial is conducted in Europe. The aim of this trial is to investigate the efficacy and safety of an intensified treatment regimen with preprandial insulin aspart and insulin detemir once or twice daily to a more convenient regimen with biphasic insulin aspart 30 twice daily on blood glucose control in subjects with type 2 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
719
HbA1c
Time frame: after 6 months of treatment
Incidence of hypoglycaemic episodes
Adverse events
Difference of HbA1c change between the two groups
Time frame: after 13 weeks of treatment
Fasting plasma glucose of treatment
Time frame: after 13 and 26 weeks
Change in weight
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Novo Nordisk Investigational Site
Graz, Austria
Novo Nordisk Investigational Site
Linz, Austria
Novo Nordisk Investigational Site
Vienna, Austria
Novo Nordisk Investigational Site
Vienna, Austria
Novo Nordisk Investigational Site
Vienna, Austria
Novo Nordisk Investigational Site
Alsdorf, Germany
Novo Nordisk Investigational Site
Altenburg, Germany
Novo Nordisk Investigational Site
Altenkirchen, Germany
Novo Nordisk Investigational Site
Altenstadt, Germany
Novo Nordisk Investigational Site
Aschaffenburg, Germany
...and 117 more locations