This study is conducted in Asia. The aim of this observational study is to evaluate the quality of life and clinical outcomes in subjects using NovoMix® 30 (biphasic insulin aspart 30) for the treatment of diabetes mellitus under normal clinical practice conditions in India.
Study Type
OBSERVATIONAL
Enrollment
24,975
Being an observational study, dose of NovoMix 30 will be according to treating physician's discretion
Novo Nordisk Investigational Site
Bangalore, India
Change in Quality of Life from baseline (using QoLD questionnaire)
Time frame: From baseline to 26 weeks of treatment
Safety
Time frame: After 26 weeks
Efficacy
Time frame: After 26 weeks
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