Efficacy and Safety of Biphasic Insulin Aspart 30 for the Treatment of Type 2 Diabetes Mellitus
NCT ID: NCT01542060
Last Updated: 2012-04-12
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
298 participants
OBSERVATIONAL
2004-01-31
2004-12-31
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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BIAsp 30 users
biphasic insulin aspart 30
Administered via an insulin injection device. Dosages varied according to individual patients' medical requirement as determined by their attending clinician
Interventions
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biphasic insulin aspart 30
Administered via an insulin injection device. Dosages varied according to individual patients' medical requirement as determined by their attending clinician
Eligibility Criteria
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Inclusion Criteria
ALL
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Novo Nordisk A/S
Principal Investigators
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Corporate Vice President for diabetes and devices
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Amman, , Jordan
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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BIASP-1892
Identifier Type: -
Identifier Source: org_study_id
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