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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


NCT number NCT00882336
Study type Observational
Source AstraZeneca
Contact
Status Completed
Phase N/A
Start date May 2009
Completion date October 2009

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