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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

NCT01492166 COMPLETED

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 sponsorNovo Nordisk A/S
StatusCOMPLETED
Enrolment1935
Start date2006-11
Completion2007-06

Conditions

Interventions

Primary outcomes

Countries

Indonesia