Switch From Premixed Human Insulin to Biphasic Insulin Aspart in the Netherlands

NCT01536626 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 211

Last updated 2017-02-24

No results posted yet for this study

Summary

This study is conducted in Europe. The aim of this observational study is to observe and investigate the process of switching from premixed human insulin 30/70 (BHI 30) to biphasic insulin aspart 30/70 (BIAsp 30) in an outpatient setting.

Conditions

Interventions

DRUG

biphasic insulin aspart 30

Prescription at the discretion of the treating physician

Sponsors & Collaborators

Principal Investigators

  • Global Clinical Registry (GCR, 1452) · Novo Nordisk A/S

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-06-09
Primary Completion
2007-04-10
Completion
2007-04-10

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01536626 on ClinicalTrials.gov