liraglutide
DrugAnonymised patient level data will be collected by the patients' own general practitioner and electronic case report form (eCRF) will be used to capture the data.
NCT Number: NCT01890993
This study is conducted in Europe. The aim of this study is to demonstrate the clinical effectiveness and safety of liraglutide and dipeptidyl peptidase-4 (DPP-4) inhibitor therapy in routine primary care in Europe.
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Observational
Paris La Défense Cedex, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Anonymised patient level data will be collected by the patients' own general practitioner and electronic case report form (eCRF) will be used to capture the data.
Time frame: Baseline (anytime within 3 months before therapy initiation), month 12 (+/-2)
Time frame: Baseline (anytime within 3 months before therapy initiation), month 12 (+/-2)
Time frame: Baseline (anytime within 3 months before therapy initiation), month 12 (+/-2)
Novo Nordisk A/S
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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