Observational Study of NovoNorm® in Subjects With Diabetes
NCT ID: NCT01498913
Last Updated: 2017-02-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
5841 participants
OBSERVATIONAL
2001-08-30
2005-03-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Repaglinide
repaglinide
Prescription with NovoNorm® 0.5mg, 1mg or 2mg tablets according to product labelling in daily clinical practice at the discretion of the physician
Interventions
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repaglinide
Prescription with NovoNorm® 0.5mg, 1mg or 2mg tablets according to product labelling in daily clinical practice at the discretion of the physician
Eligibility Criteria
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Inclusion Criteria
ALL
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Principal Investigators
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Global Clinical Registry (GCR, 1452)
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Novo Nordisk Investigational Site
Seoul, , South Korea
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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AGEE-1882
Identifier Type: -
Identifier Source: org_study_id
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