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European Study of Cardiovascular Risk (EURIKA)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Hypertension
Diabetes
Hyperlipidemia
Obesity
Cardiovascular Risk Factors
Smoking

Study type

Observational

Funder types

Industry

Identifiers

NCT00882336
NIS-CEU-DUM-2008/1

Details and patient eligibility

About

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.

Enrollment

7,200 estimated patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

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

Trial design

7,200 participants in 1 patient group

1
Description:
Patients 50+ years old, with at least one additional CV risk factor (with no previous CV event or hospitalization for a CV event)

Trial contacts and locations

778

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Data sourced from clinicaltrials.gov

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