Trial ID: | L5037 |
Source ID: | NCT00698802
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Associated Drug: |
Ex1000
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Title: |
Safety and Efficacy of Biphasic Human Insulin Compared to EX1000 in Type 2 Diabetes
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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 2
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Interventions: |
DRUG: EX1000|DRUG: biphasic human insulin
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Outcome Measures: |
Primary: HbA1c, after 8 weeks of treatment | Secondary: HbA1c, For the duration of the trial|Fructosamine, For the duration of the trial|FPG, For the duration of the trial|4-point SMPG profiles, For the duration of the trial|Incidence of hypoglycaemic episodes, For the duration of the trial|Frequency and severity of adverse events (including injection site reactions), For the duration of the trial|Laboratory safety parameters (haematology, biochemistry and lipids), For the duration of the trial|Physical examination and vital signs, For the duration of the trial|Total daily insulin dosages, For the duration of the trial
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Sponsor/Collaborators: |
Sponsor: Novo Nordisk A/S
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE2
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Enrollment: |
397
|
Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
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Start Date: |
2008-06
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Completion Date: |
2009-03
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Results First Posted: |
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Last Update Posted: |
2015-04-14
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Locations: |
Vijayawada, 520002, India|Johannesburg, Gauteng, 2193, South Africa|Abu Dhabi, 51900, United Arab Emirates
|
URL: |
https://clinicaltrials.gov/show/NCT00698802
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