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Observational Study to Observe the Safety of Levemir® Treatment in Patients With Type 2 Diabetes

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Novo Nordisk

Status

Completed

Conditions

Diabetes
Diabetes Mellitus, Type 2

Treatments

Drug: insulin detemir

Study type

Observational

Funder types

Industry

Identifiers

NCT00735501
NN304-1938

Details and patient eligibility

About

This observational study is conducted in Europe. The study aims to observe the incidence of serious adverse drug reactions in subjects with type 2 diabetes during Levemir® treatment.

Enrollment

314 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any patient with type 2 diabetes
  • Currently treated with basal human insulin therapy (basal only or in combination with oral glucose lowering drugs or other insulin)
  • Selection of patients will be at the discretion of the treating physician after the decision to prescribe one of the study products to the patient

Exclusion criteria

  • Known or suspected allergy to study product(s) or related products.
  • Pregnancy or breastfeeding or intention of becoming pregnant within the next 6 months

Trial design

314 participants in 1 patient group

A
Treatment:
Drug: insulin detemir

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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