Trial ID: | L6969 |
Source ID: | NCT00675493
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Associated Drug: |
Biphasic Insulin Aspart 30
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Title: |
Observational Study of Type 1 and Type 2 Diabetes Patients Having Switched From Human Premixes to NovoMix®30
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Acronym: |
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Status: |
COMPLETED
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Study Results: |
NO
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Results: |
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Conditions: |
Diabetes|Diabetes Mellitus, Type 1|Diabetes Mellitus, Type 2
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Interventions: |
DRUG: biphasic insulin aspart 30
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Outcome Measures: |
Primary: Change in HbA1c from baseline, For the duration of the study | Secondary: Percentage of subjects achieving HbA1c below 7.0% and below or equal to 6.5%, after 12 weeks and 24 weeks of treatment|Change in FPG (glucose variability), after 12 weeks and 24 weeks of treatment|Change in PPG (postprandial control), after 12 weeks and 24 weeks of treatment|Change in insulin dose and number of injections, at 12 weeks and 24 weeks of treatment|Change in oral antidiabetic drug therapy, after 12 weeks and 24 weeks of treatment|Change in body weight, at 12 weeks and 24 weeks of treatment|Change in number of hypoglycaemic events, during 4 weeks proceeding routine visits at 12 weeks and 24 weeks of treatment|Number of adverse drug reactions (ADR), after 12 weeks and 24 weeks of treatment
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Sponsor/Collaborators: |
Sponsor: Novo Nordisk A/S
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Gender: |
ALL
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Age: |
CHILD, ADULT, OLDER_ADULT
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Phases: |
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Enrollment: |
942
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Study Type: |
OBSERVATIONAL
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Study Designs: |
Observational Model: |Time Perspective: p
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Start Date: |
2008-05
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Completion Date: |
2009-01
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Results First Posted: |
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Last Update Posted: |
2016-02-19
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Locations: |
Bucharest, 010031, Romania
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URL: |
https://clinicaltrials.gov/show/NCT00675493
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