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A Multi-center, Prospective, Non-interventional Evaluation of Efficacy, Safety and Convenience of Mixtard® 30 NovoLet® as Monotherapy, or in Combination With Oral Hypoglycaemic Agent ( OHA ), in Treatment of Subjects With Type 2 Diabetes in Routine Clinical Practice
This study is conducted in Asia. The aim of this study is to assess the efficacy, safety and convenience of the use of Mixtard® 30 NovoLet® used alone or combined with oral hypoglycaemic agent (OHA) in the management of type 2 diabetes mellitus in an out-patient setting.
Details
| Lead sponsor | Novo Nordisk A/S |
|---|---|
| Status | COMPLETED |
| Enrolment | 1935 |
| Start date | 2006-11 |
| Completion | 2007-06 |
Conditions
- Diabetes
- Diabetes Mellitus, Type 2
Interventions
- biphasic human insulin 30
Primary outcomes
- Change in fasting blood glucose (FBG)
- Change in 2-hour post prandial blood glucose
- Change in HbA1c (glycosylated haemoglobin)
- Change in prandial glucose increment (PGI)
Countries
Indonesia