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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT01585506 |
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Date of registration:
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26/03/2012 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Psychosocial Factors Related to Compliance With Treatment With Biphasic Insulin Analogues
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Scientific title:
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Psychosocial Factors Related to Compliance With Treatment With Biphasic Insulin Analogues |
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Date of first enrolment:
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September 20, 2010 |
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Target sample size:
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3618 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT01585506 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Poland
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Contacts
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Name:
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Global Clinical Registry (GCR, 1452) |
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Address:
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Telephone:
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Email:
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Affiliation:
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Novo Nordisk A/S |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients with type 2 diabetes in whom therapy with biphasic insulin analogues was
started
Age minimum:
N/A
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Diabetes
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Diabetes Mellitus, Type 2
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Intervention(s)
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Other: No treatment given
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Primary Outcome(s)
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Frequency and level of difficulty in introducing changes in compliance with the guidelines for biphasic insulin analogue use in subjects previously treated with biphasic human insulins
[Time Frame: Up to 3 months]
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Secondary Outcome(s)
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Correlations between the difficulty in introducing changes in compliance with the guidelines for biphasic insulin analogue use in subjects previously treated with biphasic human insulins, and psychosocial factors
[Time Frame: Up to 3 months]
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Secondary ID(s)
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BIASP-4018
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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