Observational Study of Patients Using NovoMix® 30 or Levemir® for Treatment of Type 1 or Type 2 Diabetes
NCT ID: NCT00665093
Last Updated: 2017-01-09
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
1569 participants
OBSERVATIONAL
2007-05-31
2008-01-31
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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A
biphasic insulin aspart 30
Start dose and frequency prescribed by the physician as a result of a normal clinical evaluation
B
insulin detemir
Start dose and frequency prescribed by the physician as a result of a normal clinical evaluation
Interventions
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biphasic insulin aspart 30
Start dose and frequency prescribed by the physician as a result of a normal clinical evaluation
insulin detemir
Start dose and frequency prescribed by the physician as a result of a normal clinical evaluation
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* NovoMix® 30 above 18 yrs
* Patients with Type 1 or Type 2 diabetes, including newly diagnosed
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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Novo Nordisk Investigational Site
Skopje, , North Macedonia
Countries
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References
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Milenkovic T. Significant Improvements in Glycemic Control with BIAsp 30 in Clinical Reality: Experience from clinical practice in Macedonia. ADA American Diabetes Association 2009; Country: USA City: New Orleans
Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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BIASP-1894
Identifier Type: -
Identifier Source: org_study_id
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