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Centralized Pan-Russian Survey on the Undertreatment of Hypercholesterolemia (CEPHEUS)

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AstraZeneca

Status

Completed

Conditions

Dyslipidaemia

Study type

Observational

Funder types

Industry

Identifiers

NCT01221584
NIS-CRU-DUM-2010/1

Details and patient eligibility

About

The purpose of the study is to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the All-Russian Scientific Cardiology Society guidelines/ the 4th Joint European Task Force guidelines.

Enrollment

1,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject must be 18 years of age or older of either gender or race.
  • Subject must provide informed consent and comply with the survey procedures.
  • Subject is on lipid lowering drug treatment for at least 3 months, with no dose change for a minimum of 6 weeks.

Exclusion criteria

  • Subjects who are unwilling or unable to provide informed consent

Trial design

1,000 participants in 1 patient group

1
Description:
Subject 18 years of age or older on lipid lowering drug treatment for at least 3 months, with no dose change for a minimum of 6 weeks..

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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