Polish Survey on the Efficacy of the Hypercholesterolemia Treatment
NCT ID: NCT01243255
Last Updated: 2012-04-04
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
1500 participants
OBSERVATIONAL
2010-12-31
2011-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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1
Patients with hypercholesterolemia on lipid lowering pharmacological treatment
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Lipid lowering drug treatment lasting at least 3 months
* No lipid lowering drug/dose change for a minimum 6 weeks prior to enrolment to the study
Exclusion Criteria
* Lack of the blood sample taken for lipid profile and glucose within 10 days before or after assessment of the patient
18 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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Principal Investigators
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Prof. Artur Mamcarz
Role: PRINCIPAL_INVESTIGATOR
Medical University of Warsaw
Barbara Możejko-Pastewka
Role: STUDY_DIRECTOR
AstraZeneca Pharma
Other Identifiers
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NIS-CPL-DUM-2010/1
Identifier Type: -
Identifier Source: org_study_id
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