Observational Study of Patients With Diabetes Using Levemir® FlexPen®
NCT ID: NCT00670683
Last Updated: 2016-03-03
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
797 participants
OBSERVATIONAL
2007-07-31
2009-09-30
Brief Summary
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The aim of this observational study is to evaluate the short term and the long term safety and efficacy of Levemir® FlexPen®. The study is planned and conducted as per requirement from Korea Food and Drug Administration (KFDA).
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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A
insulin detemir
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
Interventions
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insulin detemir
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
Eligibility Criteria
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Inclusion Criteria
Exclusion 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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Pusan, , South Korea
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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NN304-1914
Identifier Type: -
Identifier Source: org_study_id
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