This observational study is conducted in Europe. The aim of this non-interventional (observational) study is to evaluate the efficacy of liraglutide (Victoza®) and to assess the conditions of use of Victoza® in daily medical practice in France.
Study Type
OBSERVATIONAL
Enrollment
3,152
Prescription is done at the discretion of the prescribing physician as part of normal clinical routine.
Novo Nordisk Investigational Site
Paris La Défense Cedex, France
Percentage of patients still in liraglutide treatment and having a HbA1c (glycosylated haemoglobin) value below 7.0%
Time frame: Month 24
Change in HbA1c at month 3
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Change in HbA1c at month 6
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Change in HbA1c at month 12
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Change in HbA1c at month 18
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Change in HbA1c at month 24
Time frame: Month 0, Month 24
Change in fasting plasma glucose (FPG) at month 3
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Change in fasting plasma glucose (FPG) at month 6
Time frame: Month 0, Month 6
Change in fasting plasma glucose (FPG) at month 12
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Change in fasting plasma glucose (FPG) at month 18
Time frame: Month 0, Month 18
Change in fasting plasma glucose (FPG) at month 24
Time frame: Month 0, Month 24
Change in Body Weight at Month 3
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Change in Body Weight at Month 6
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Change in Body Weight at Month 12
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Change in Body Weight at Month 18
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Change in Body Weight at Month 24
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