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Centralised Pan-European Survey on the Undertreatment of Hyperchlesterolemia - CEPHEUS

Conditions
Patients on lipid-lowering pharmacological treatment
Registration Number
EUCTR2006-000954-31-FI
Lead Sponsor
AstraZeneca Oy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
20900
Inclusion Criteria

-Subject must be 18 years of age or older of either sex and of any race.
-Subject must demonstrate his/her willingness to participate in the survey and comply with its procedures by signing a written informed consent.
-Subject is on lipid-lowering drug treatment for at least 3 months, with no dose change for a minimum of 6 weeks.

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

-Subjects who are unwilling or unable to provide informed consent.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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