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European Study of Cardiovascular Risk

Epidemiological Study of European Cardiovascular Risk Patients: Disease Prevention and Management in Usual Daily Practice

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00882336
Acronym
EURIKA
Enrollment
7200
Registered
2009-04-16
Start date
2009-05-31
Completion date
2009-10-31
Last updated
2009-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factors, Diabetes, Hyperlipidemia, Hypertension, Obesity, Smoking

Keywords

Cardiovascular risk management, Hyperlipidemia, Hypertension, Diabetes, Obesity

Brief summary

The main objective of this study is to describe the management of patients with cardiovascular risk factors in primary prevention among different European countries. The patient's participation consists of a single study visit during a routine visit of the patient to the clinic/office. Study variables will be measured: * By an interview between physician and patient during the visit and/or available medical records' information: social and demographic patient characteristics, relevant family medical history, current medication. * By questions asked to the physician: physician perception of patients' CV risk factor, guidelines adherence and cost-containment. * By measurement performed to the patient during the visit: weight, height, BMI, waist and hip circumference will be measured. * CV risk factors (blood parameters) will be measured by collecting available data documented within the last year in the medical records and by the collection and analyses of a blood sample during the visit.

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Provision of informed consent. * Patients 50+ years old, with at least one additional CV risk factor (with no previous CV event or hospitalisation for a CV event) from Primary Care or hospital outpatient clinic.

Exclusion criteria

* Subjects who are unwilling or unable to provide informed consent * Previous CV disease event or hospitalisation for a CV event * Current participation in a clinical trial

Design outcomes

Primary

MeasureTime frame
LDL-cholesterol, systolic and diastolic blood pressure, Tot. cholesterol, Non-HDL cholesterol, HDL-cholesterol, waist and hip circumference, HbA1cCross-sectional
Gender, age, patients with diabetes and/or hypertension (%), smoker status, family medical history.Cross-sectional

Secondary

MeasureTime frame
BMI, Score based 10 year CHD mortality > 5%, High Risk patients (no. and %)Cross-sectional
Use of concomitant medication: anticoagulant, anti hypertensive, antidiabetic, lipid-lowering drugsCross-sectional
Biomarkers: Apo-A1, Apo-B, Hs-CRP, Creatinine, albuminuria, uric acid, glomerular filtration rate.Cross-sectional

Countries

Austria, Belgium, France, Germany, Greece, Norway, Russia, Spain, Sweden, Switzerland, Turkey (Türkiye), United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026