Safety of Treatment Initiation With Biphasic Insulin Aspart 30 in Hospitalised Patients With Type 2 Diabetes
NCT ID: NCT01565733
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
2223 participants
OBSERVATIONAL
2007-01-31
2007-07-31
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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NovoMix® 30 users
biphasic insulin aspart 30
Biphasic insulin aspart 30 prescribed solely on the basis of clinical judgement. Initial dose, frequency of injections and further dosage amendments at the discretion of the treating physician.
Interventions
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biphasic insulin aspart 30
Biphasic insulin aspart 30 prescribed solely on the basis of clinical judgement. Initial dose, frequency of injections and further dosage amendments at the discretion of the treating physician.
Eligibility Criteria
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Inclusion Criteria
* Treated with oral anti-diabetics and/or human insulin
Exclusion Criteria
* Hypersensitive to biphasic insulin aspart or any of the excipients
* Pregnant or lactating women, or those who plan to get pregnant within the next 12 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
Warsaw, , Poland
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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BIASP-4017
Identifier Type: -
Identifier Source: org_study_id