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Polish Survey on the Efficacy of the Hypercholesterolemia Treatment (CEPHEUS)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Hypercholesterolemia

Study type

Observational

Funder types

Industry

Identifiers

NCT01243255
NIS-CPL-DUM-2010/1

Details and patient eligibility

About

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.

Enrollment

1,500 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

1,500 participants in 1 patient group

1
Description:
Patients with hypercholesterolemia on lipid lowering pharmacological treatment

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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