Preference Study Between NovoFine® Autocover™ and a NovoFine® 8 mm Needle
NCT ID: NCT01024218
Last Updated: 2017-02-24
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
PHASE4
78 participants
INTERVENTIONAL
2004-12-01
2005-04-26
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Interventions
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NovoFine® needle 8 mm
autocover needle
Eligibility Criteria
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Inclusion Criteria
* Participants must demonstrate proficiency with the injection device in the handling test prior to testing the NovoFine® Autocover™ Needle in patients
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
Copenhagen, , Denmark
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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AUTOCOVER
Identifier Type: -
Identifier Source: org_study_id
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