Observational Study of Patients Using NovoMix® 30 or Levemir® for Treatment of Type 1 or Type 2 Diabetes
NCT ID: NCT00671008
Last Updated: 2024-01-02
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
400 participants
OBSERVATIONAL
2007-12-31
2008-09-30
Brief Summary
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The aim of this observational study is to evaluate the glycaemic control in patients with type 1 or 2 diabetes using NovoMix® 30 or Levemir® under normal clinical practice conditions.
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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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A
biphasic insulin aspart 30
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
B
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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biphasic insulin aspart 30
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
insulin detemir
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age: Levemir® above 6 years
* Age: Novomix® above 18 years
Exclusion Criteria
6 Years
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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Sarajevo, , Bosnia and Herzegovina
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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NN304-1964
Identifier Type: -
Identifier Source: org_study_id
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