An Observational Study of Efficacy and Safety of Modern Insulin in Diabetes Patients Switched From Anti-diabetic Treatment
NCT ID: NCT00698269
Last Updated: 2016-10-28
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
5926 participants
OBSERVATIONAL
2008-02-29
2009-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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A
insulin detemir
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
B
biphasic insulin aspart 30
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
C
insulin aspart
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
Interventions
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insulin detemir
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
biphasic insulin aspart 30
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
insulin aspart
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
* Treatment with any diabetes treatment other than NovoMix® 30, Levemir® and/or NovoRapid®
* Selection will be at the discretion of the individual physician
Exclusion Criteria
* Previous enrolled in this study
* Hypersensitivity to Levemir®, NovoMix® 30 and/or NovoRapid® or to any of the excipients
* Women who are pregnant, breast feeding or have the intention of becoming pregnant within 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
Riyadh, , Saudi Arabia
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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INS-3532
Identifier Type: -
Identifier Source: org_study_id