This trial is conducted in Europe and Oceania. The aim of this trial is to assess the effects of liraglutide on energy intake in subjects with type 2 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
43
1.8 mg/day injected subcutaneously for 4 weeks
Liraglutide placebo, injected subcutaneously for 4 weeks
Glimepiride placebo, dose individually adjusted, administered orally for 4 weeks
Novo Nordisk Investigational Site
Adelaide, South Australia, Australia
Novo Nordisk Investigational Site
Neuss, Germany
The energy intake at a standardised buffet meal with a preload paradigm quantified using Foodworks 2.10
The energy intake at a standardised buffet meal without a preload paradigm quantified using Foodworks 2.10
Macronutrient distribution of food consumed at a standardised buffet meal with a preload paradigm quantified using Foodworks 2.10
Macronutrient distribution of food consumed at a standardised buffet meal without a preload paradigm quantified using Foodworks 2.10
Total duration of eating at the buffet meal (satiation)
Weight
Waist circumference
Adverse events
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Dose individually adjusted, administered orally for 4 weeks