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Observational Study on Efficacy, Safety and Convenience of Using Mixtard® 30 NovoLet® Alone or Combined With OHA in Treatment of Type 2 Diabetes in Routine Clinical Practice

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Novo Nordisk

Status

Completed

Conditions

Diabetes
Diabetes Mellitus, Type 2

Treatments

Drug: biphasic human insulin 30

Study type

Observational

Funder types

Industry

Identifiers

NCT01492166
NOPEN3-1890

Details and patient eligibility

About

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.

Enrollment

1,935 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Type 2 diabetes
  • Not adequately controlled on their current therapy

Trial design

1,935 participants in 1 patient group

Novolet®
Treatment:
Drug: biphasic human insulin 30

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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