Observational Study With InnoLet® in Daily Clinical Practice

NCT01492959 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1030

Last updated 2017-02-28

No results posted yet for this study

Summary

This study is conducted in Asia. The aim of this study is to review the efficacy and safety of insulin treatment with InnoLet® in daily clinical practice.

Conditions

  • Diabetes
  • Diabetes Mellitus, Type 1
  • Diabetes Mellitus, Type 2

Interventions

DRUG

insulin human

Insulin human delivered with the InnoLet® device was prescribed according to product labelling to subjects in need of insulin treatment

Sponsors & Collaborators

Principal Investigators

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

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-03-23
Primary Completion
2005-03-23
Completion
2005-03-23

Countries

  • South Korea

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 NCT01492959 on ClinicalTrials.gov