2,302
Participants
Start Date
December 8, 2015
Primary Completion Date
August 12, 2016
Study Completion Date
August 12, 2016
No treatment given
Information will be collected from the medical records (paper/electronic) of each patient at several outpatient clinics to describe the two periods of medical history: before and after the initiation date of Tresiba®. For each patient, data will be collected, to describe a minimum of 6 months to a maximum of 12 months in each period; thus, the study will collect information on 12 to 24 months of medical history for each patient.
Novo Nordisk Investigational Site, Vienna
Novo Nordisk Investigational Site, Vienna
Novo Nordisk Investigational Site, Gentofte Municipality
Novo Nordisk Investigational Site, Sankt Gallen
Novo Nordisk Investigational Site, München
Novo Nordisk Investigational Site, Athens
Novo Nordisk Investigational Site, Perugia
Lead Sponsor
Novo Nordisk A/S
INDUSTRY