Observational Study to Observe the Efficacy of Levemir® (Insulin Detemir) in Patients With Type 2 Diabetes.
NCT ID: NCT00793273
Last Updated: 2014-08-15
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
1074 participants
OBSERVATIONAL
2008-11-30
2011-01-31
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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A
insulin detemir
Effectiveness and safety data collection in connection with the use of the drug Levemir® in daily clinical practice
Interventions
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insulin detemir
Effectiveness and safety data collection in connection with the use of the drug Levemir® in daily clinical practice
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Insulin-naive or currently treated with another basal insulin
* Inclusion of patients at the discretion of the treating physician after the decision to prescribe Levemir®
Exclusion Criteria
* Patients treated with short acting or with premix insulin
* Women who are pregnant, breast feeding or have the intention to become pregnant
* Known or suspected allergy to the study product or related product
18 Years
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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Zurich, Oerlikon, Switzerland
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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NN304-3694
Identifier Type: -
Identifier Source: org_study_id
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