This trial is conducted in Europe. The aim of this trial is to evaluate safety and efficacy in children with type 1 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Injected s.c. (under the skin) three times a day
Injected s.c. (under the skin) 30 minutes before the meals
May be administered s.c. (under the skin) in both treatment groups thrice daily
Novo Nordisk Investigational Site
Berlin, Germany
Novo Nordisk Investigational Site
Dresden, Germany
Novo Nordisk Investigational Site
Hagen, Germany
Novo Nordisk Investigational Site
Hamburg, Germany
Incidence of hypoglycaemic episodes during the treatment
Time frame: Week 0; week 24
Change in HbA1c (glycosylated haemoglobin A1c)
Time frame: Week 0; week 24
Incidence of Adverse Events (AEs)
Time frame: Week 0; week 24
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Novo Nordisk Investigational Site
Hanover, Germany
Novo Nordisk Investigational Site
Osnabrück, Germany