This study is conducted in Asia. The aim of this observational study is to compare the clinical safety profile and effectiveness of NovoMix® 30 and Levemir™ for the treatment of diabetes in the Philippines.
Study Type
OBSERVATIONAL
Enrollment
3,131
Evaluation of the safety profile and effectiveness of biphasic insulin aspart 30 in the treatment of diabetes mellitus under normal clinical practice conditions in the Philippines
Evaluation of the safety profile and effectiveness of insulin detemir in the treatment of diabetes mellitus under normal clinical practice conditions in the Philippines
Novo Nordisk Investigational Site
Manila, Philippines
Number of all (Major/Minor/Nocturnal) hypoglycaemic events, reported as serious adverse drug reactions.
Time frame: during 12 months of treatment
HbA1c
Time frame: at the end of the study
FBG (Fasting Blood Glucose)
Time frame: at the end of the study
Average (mean) fasting plasma glucose level
Time frame: at the end of the study
Number of minor (including nocturnal) hypoglycaemic events
Time frame: during 12 months of treatment
Number of major (including nocturnal) hypoglycaemic events
Time frame: during 12 months of treatment
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