Observational Study to Observe the Safety of NovoMix® 30 Treatment in Patients With Type 2 Diabetes
NCT ID: NCT00729898
Last Updated: 2016-10-31
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
243 participants
OBSERVATIONAL
2008-03-31
2010-09-30
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 30
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
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Currently treated with basal human insulin therapy (basal only or in combination with oral glucose lowering drugs or other insulin
* Selection of patients will be at the discretion of the treating physician after the decision to prescribe one of the study products to the patient
Exclusion Criteria
* Pregnancy, breast-feeding or intention of becoming pregnant within the next 6 months
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
Rud, , Norway
Novo Nordisk Investigational Site
Farsta, , Sweden
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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BIASP-3512
Identifier Type: -
Identifier Source: org_study_id