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Clinical Trials/NCT00375336
NCT00375336
Unknown
N/A

Risk Markers of Coronary Artery Disease Associated With Calcific Aortic Valve Disease

Charles University, Czech Republic1 site in 1 country300 target enrollmentJanuary 2005

Overview

Phase
N/A
Intervention
Not specified
Conditions
Aortic Stenosis
Sponsor
Charles University, Czech Republic
Enrollment
300
Locations
1
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is

  • to determine the degree of endothelial dysfunction and inflammation in calcific aortic valve disease associated with coronary artery disease(CAD).
  • to determine whether there is relationship between calcium metabolism and calcific aortic valve disease associated with CAD.

Detailed Description

Cardiovascular disease, mainly coronary artery disease, causes more than one half of deaths in the developed countries. Only recently, calcific aortic valve disease, was proved to belong to the family of atherosclerosis. It is associated with higher cardiovascular morbidity and mortality, the cause of which is not entirely clear. The link to significant coronary artery disease, probably, is of highest importance. We compare groups of patients with coronary artery disease and calcific stenotic, sclerotic or intact aortic valve. The aim is to assess and compare their risk profile to verify our hypothesis that, within significant coronary artery disease, calcific aortic valve identifies a subgroup of patients with higher cardiovascular risk, assessed by endothelial dysfunction and the two year follow-up of cardiovascular events on optimally set treatment. Further, we study the possible association of valvular calcification and calcium metabolism in patients with normal kidney function.

Registry
clinicaltrials.gov
Start Date
January 2005
End Date
December 2008
Last Updated
17 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Charles University, Czech Republic

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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