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An Observational Study Evaluating Efficacy, Safety and Convenience of NovoNorm® in Treatment of Type 2 Diabetes in Routine Clinical Practice

Novo Nordisk logo

Novo Nordisk

Status

Completed

Conditions

Diabetes
Diabetes Mellitus, Type 2

Treatments

Drug: repaglinide

Study type

Observational

Funder types

Industry

Identifiers

NCT01498900
AGEE-1875

Details and patient eligibility

About

This study is conducted in Africa and Asia. The aim of this study is to evaluate the efficacy, safety and convenience of using repaglinide (NovoNorm®) in type 2 diabetes management in routine clinical practice.

Enrollment

30,554 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Type 2 diabetes
  • Newly diagnosed or not adequately controlled with current therapy

Trial design

30,554 participants in 1 patient group

Repaglinide
Treatment:
Drug: repaglinide

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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