Polish Survey on the Efficacy of the Hypercholesterolemia Treatment

NCT ID: NCT01243255

Last Updated: 2012-04-04

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

1500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-12-31

Study Completion Date

2011-06-30

Brief Summary

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The purpose of the survey is to evaluate the efficacy of treatment of hypercholesterolemia in Polish patients who are currently on lipid- lowering pharmacological therapy . Efficient treatment is defined as achievement of the LDL cholesterol level goals according to the European Society of Cardiology 2007 guidlines.

Detailed Description

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Conditions

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Hypercholesterolemia

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

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

* Patients on lipid lowering drug treatment
* 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 patient's signed informed consent form
* Lack of the blood sample taken for lipid profile and glucose within 10 days before or after assessment of the patient
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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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