Observational Study to Evaluate the Safety and Efficacy of NovoMix® 70 in Type 2 Diabetes
NCT ID: NCT00704223
Last Updated: 2014-06-24
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
619 participants
OBSERVATIONAL
2008-05-31
2008-11-30
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
Start dose and frequency to prescribed by the physician as a result of a normal clinical evaluation
Interventions
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biphasic insulin aspart
Start dose and frequency to 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
* HbA1c over 7%
* No contraindication with NovoMix® 70
Exclusion Criteria
* Subjects participating in a clinical trial or another observational study
* Subjects under previous basis-bolus insulin therapy
* Women who are pregnant, breast feeding and women of child bearing capacity who are not using any reliable contraceptive method
18 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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Vienna, , Austria
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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BIASP-3576
Identifier Type: -
Identifier Source: org_study_id
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