insulin detemir
DrugStart dose and frequency as well as dose alterations to be determined by the physician according to normal clinical evaluation
Other names: Levemir®
NCT Number: NCT00735501
This observational study is conducted in Europe. The study aims to observe the incidence of serious adverse drug reactions in subjects with type 2 diabetes during Levemir® treatment.
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Notify Me18 year and older
All sexes
Observational
Copenhagen S, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Start dose and frequency as well as dose alterations to be determined by the physician according to normal clinical evaluation
Other names: Levemir®
Time frame: After 26 weeks
Time frame: at 12 weeks and 26 weeks
Time frame: after 12 and 26 weeks
Time frame: at 12 and 26 weeks
Time frame: at 12 and 26 weeks
Time frame: at 12 and 26 weeks
Novo Nordisk A/S
Industry
Safety of Levemir® (Insulin Detemir) Treatment in Patients With Type 2 Diabetes
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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